659 results on '"A. Jelcic"'
Search Results
102. Identification of four novel T cell autoantigens and personal autoreactive profiles in multiple sclerosis
- Author
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Bronge, Mattias, Hogelin, Klara Asplund, Thomas, Olivia G., Ruhrmann, Sabrina, Carvalho-Queiroz, Claudia, Nilsson, Ola B., Kaiser, Andreas, Zeitelhofer, Manuel, Holmgren, Erik, Linnerbauer, Mathias, Adzemovic, Milena Z., Hellstrom, Cecilia, Jelcic, Ivan, Liu, Hao, Nilsson, Peter, Hillert, Jan, Brundin, Lou, Fink, Katharina, Kockum, Ingrid, Tengvall, Katarina, Martin, Roland, Tegel, Hanna, Graslund, Torbjorn, Al Nimer, Faiez, Guerreiro-Cacais, Andre Ortlieb, Khademi, Mohsen, Gafvelin, Guro, Olsson, Tomas, Gronlund, Hans, Bronge, Mattias, Hogelin, Klara Asplund, Thomas, Olivia G., Ruhrmann, Sabrina, Carvalho-Queiroz, Claudia, Nilsson, Ola B., Kaiser, Andreas, Zeitelhofer, Manuel, Holmgren, Erik, Linnerbauer, Mathias, Adzemovic, Milena Z., Hellstrom, Cecilia, Jelcic, Ivan, Liu, Hao, Nilsson, Peter, Hillert, Jan, Brundin, Lou, Fink, Katharina, Kockum, Ingrid, Tengvall, Katarina, Martin, Roland, Tegel, Hanna, Graslund, Torbjorn, Al Nimer, Faiez, Guerreiro-Cacais, Andre Ortlieb, Khademi, Mohsen, Gafvelin, Guro, Olsson, Tomas, and Gronlund, Hans
- Abstract
Multiple sclerosis (MS) is an inflammatory disease of the central nervous system (CNS), in which pathological T cells, likely autoimmune, play a key role. Despite its central importance, the autoantigen repertoire remains largely uncharacterized. Using a novel in vitro antigen delivery method combined with the Human Protein Atlas library, we screened for T cell autoreactivity against 63 CNS-expressed proteins. We identified four previously unreported autoantigens in MS: fatty acid-binding protein 7, prokineticin-2, reticulon-3, and synaptosomal-associated protein 91, which were verified to induce interferon-gamma responses in MS in two cohorts. Autoreactive profiles were heterogeneous, and reactivity to several autoantigens was MS-selective. Autoreactive T cells were predominantly CD4(+) and human leukocyte antigen-DR restricted. Mouse immunization induced antigen-specific responses and CNS leukocyte infiltration. This represents one of the largest systematic efforts to date in the search for MS autoantigens, demonstrates the heterogeneity of autoreactive profiles, and highlights promising targets for future diagnostic tools and immunomodulatory therapies in MS.
- Published
- 2022
- Full Text
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103. Combined Genetic Ablation of CD54 and CD58 in CAR Engineered Cytotoxic Lymphocytes Effectively Averts Allogeneic Immune Cell Rejection
- Author
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Hammer, Quirin, Perica, Karlo, Mbofung, Rina M., van Ooijen, Hanna, Varady, Erika, Jelcic, Mark, Pan, Yijia, Momayyezi, Pouria, Groff, Brian, Abujarour, Ramzey, Krokeide, Silje Zandstra, Lee, Tom, Williams, Alan M., Goodridge, Jode P., Valamehr, Bahram, Önfelt, Björn, Sadelain, Michel, Malmberg, Karl-Johan, Hammer, Quirin, Perica, Karlo, Mbofung, Rina M., van Ooijen, Hanna, Varady, Erika, Jelcic, Mark, Pan, Yijia, Momayyezi, Pouria, Groff, Brian, Abujarour, Ramzey, Krokeide, Silje Zandstra, Lee, Tom, Williams, Alan M., Goodridge, Jode P., Valamehr, Bahram, Önfelt, Björn, Sadelain, Michel, and Malmberg, Karl-Johan
- Abstract
Allogeneic cell therapies hold promise to be cost effective with scaled manufacturing for multi-dosing and on-demand off-the-shelf availability. A critical consideration for allogeneic cell products is their ability to persist, maintain function and avoid rejection by the patient's immune system. Genetic knockout (KO) of beta-2-microglobulin (B2M) leads to complete loss of cell-surface human leukocyte antigen (HLA) class I expression and efficiently abrogates CD8+ T-cell reactivity. However, loss of HLA class I triggers NK cell-mediated missing-self recognition and manipulation of B2M must therefore be combined with other immune-modulating strategies to limit recipient NK cell reactivity.We hypothesized that rejection by the patient's immune system can be diminished in primary CAR T cells, iPSC-derived T (iT) and NK (iNK) cells by reverse-engineering common tumor escape mechanisms. The adhesion molecules CD54 and CD58 are both present at the target cell side of the immune synapse, and loss of either of these molecules have previously been reported to elicit immune escape. Here, we show that the combined deletion of CD54 and CD58 in allogeneic immune effector cells makes them resistant to rejection by recipient immune cells through unidirectional reduced synapse formation (Figure 1A).HLA class I down-regulation by B2M silencing in primary T and NK cells triggered potent cytotoxicity by resting allogeneic NK cells. This response was mostly driven by educated NK cells expressing either NKG2A or killer cell immunoglobulin-like receptors (KIR) binding to HLA-E and HLA-C, respectively. However, over-expression of HLA-E or single HLA-C ligands in a K562 screening model only shut down the specific response of the NK cell subset carrying the cognate inhibitory receptor, resulting in only partial resistance to NK cells at the bulk level. Notably, the introduction of HLA-E was particularly detrimental in donors with expanded NKG2C+ NK cell subsets, due to its stimulatory effec, QC 20230316
- Published
- 2022
- Full Text
- View/download PDF
104. SARS-CoV-2 infection and venous thromboembolism after surgery: an international prospective cohort study
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Nepogodiev, D., Simoes, J. F. F., Li, E., Picciochi, M., Glasbey, J. C., Baiocchi, G., Blanco-Colino, R., Chaudhry, D., Alameer, E., El-Boghdadly, K., Wuraola, F., Ghosh, D., Gujjuri, R. R., Harrison, E. M., Lule, H., Kaafarani, H., Khosravi, M., Kronberger, I., Leventoglu, S., Mann, H., Mclean, K. A., Mengesha, M. G., Modolo, M. M., Ntirenganya, F., Norman, L., Outani, O., Pius, R., Pockney, P., Qureshi, A. U., Roslani, A. C., Satoi, S., Shaw, C., Bhangu, A., Omar, O. M., Ahmed, W. -U. -R., Argus, L., Ball, A., Bywater, E. P., Brar, A., Dawson, B. E., Duran, I., Elhadi, M., Jones, C. S., Kamarajah, S. K., Keatley, J. M., Lawday, S., Marson, E. J., Ots, R., Santos, I., Taylor, E. H., Trout, I. M., Varghese, C., Venn, M. L., Xu, W., Dajti, I., Gjata, A., Kacimi, S. E. O., Boccalatte, L., Cox, D., Townend, P., Aigner, F., Kronberger, I. E., Samadov, E., Alderazi, A., Hossain, K., Padmore, G., van Ramshorst, G., Lawani, I., Cerovac, A., Delibegovic, S., Gomes, G. M. A., Buarque, I. L., Gohar, M., Slavchev, M., Nwegbu, C., Agarwal, A., Martin, J., Ng-Kamstra, J., Olivos, M., Lou, W., Ren, D. -L., Calvache, J. A., Perez Rivera, C. J., Hadzibegovic, A. D., Kopjar, T., Mihanovic, J., Jimenez, P. M. A., Gouvas, N., Klat, J., Novysedlak, R., Amisi, N., Christensen, P., El-Hussuna, A., Batista, S., Lincango-Naranjo, E., Emile, S., Sandoval, D. A. A., Dhufera, H., Hailu, S., Kauppila, J. H., Arnaud, A. P., Demetrashvili, Z., Albertsmeier, M., Lederhuber, H., Loffler, M. W., Acquah, D. K., Ofori, B., Tabiri, S., Metallidis, S., Tsoulfas, G., Aguilera-Arevalo, M. -L., Recinos, G., Mersich, T., Wettstein, D., Kembuan, G., Milan, P. B., Khosravi, M. H., Mozafari, M., Hilmi, A., Mohan, H., Zmora, O., Gallo, G., Pata, F., Pellino, G., Fujimoto, Y., Kuroda, N., Abou Chaar, M. K., Ayasra, F., Fakhradiyev, I., Hamdun, I. H. S., Jin-Young, J., Jamal, M., Karout, L., Gulla, A., Rasoaherinomenjanahary, F., Samison, L. H., Sanchez, I. I. D., Gonzalez, D. S., Martinez, L., Martinez, M. J., Nayen, A., la Medina, A. R. -D., Nunez, J., Nashidengo, P. R., Shah, R., Shrestha, A. L., Jonker, P., Kruijff, S., Noltes, M., Steinkamp, P., Wright, D., Abdur-Rahman, L., Ademuyiwa, A., Adisa, A., Osinaike, B., Seyi-Olajide, J., Williams, O., Williams, E., Pejkova, S., Al Balushi, Z., Sayyed, R., Mohsen, M. A., Abukhalaf, S. A., Cukier, M., Gomez-Fernandez, H., Yip, S. S., Ojeda, X. P. V., Sacdalan, M. D., Major, P., Azevedo, J., Cunha, M. F., Zarour, A., Bonci, E. -A., Negoi, I., Efetov, S., Kochetkov, V., Litvin, A., Ingabire, J. A., Bucyibaruta, G., Faustin, N., Habumuremyi, S., Imanishimwe, A., de Dieu, H. J., Munyaneza, E., Ncogoza, I., Ndong, A., Radenkovic, D., Chew, M. H., Koh, F., Ngu, J., Panyko, A., Bele, U., Kosir, J. A., Daoud, H., Bravo, A. M. M., Jayarajah, U., Wickramasinghe, D., Adam, M. E. A. E., Rutegard, M., Sund, M., Adamina, M., Gialamas, E., Horisberger, K., Alshaar, M., Huang, A., Lohsiriwat, V., Charles, S., Jlassi, H., Isik, A., Lekuya, H. M., Kopetskyi, S., Alsaadi, H., Alshryda, S., Alser, O., Bankhead-Kendall, B., Breen, K., Mashbari, H., Cal, F. B., Al-Naggar, H., Maimbo, M., Mazingi, D., Abbott, T., Akhbari, M., Benson, R., Bhanderi, S., Biccard, B., Caruana, E., Chakrabortee, S., Chapatwala, R., Costas-Chavarri, A., Demetriades, A. K., Desai, A., Di Saverio, S., Drake, T., Edwards, J., Evans, J., Fiore, M., Ford, S., Fotopoulou, C., Fowler, A., Futaba, K., Ganly, I., James, H. G., Griffiths, E., Gronchi, A., Hutchinson, P., Hyman, G. Y., Incorvia, J., Jain, R., Jenkinson, M., Khan, T., Knight, S. R., Kolias, A., Kudsk-Iversen, S., Kwan, T. Y., Leung, E., Mayol, J., Mckay, S., Meara, J. G., Mills, E., Moug, S., Patel, A., Perinotti, R., Rice, H. E., Roberts, K., Schache, A., Shaw, R., Smart, N., Stephens, M., Stewart, G. D., Teasdale, E., Vaughan-Shaw, P., Vidya, R., Wright, N., Zimmelman, N., Agastra, E., Thereska, D., Lucchini, S. M., Laudani, V., Chwat, C., Salazar, I. I. P., Pachajoa, D. A. P., Duro, A., Arancibia, J. A. C., D'Aulerio, G., Dudi-Venkata, N., Egoroff, N., Farik, S., Lott, N., Moss, J. -L., Rennie, S., Tan, L., Vo, U. G., Watson, D., Watters, D., Bright, T., Hollington, P., Zhou, X., Kroon, H. M., Farfus, A., Barker, J., Watson, E., Stevens, S., Latif, H., Dawson, A. C., Chuan, A., Muralidharan, V., Wong, E., Ackermann, T., Pacilli, M., Hodgson, R., Heriot, A., Choong, P., Brown, W., Lidder, S., Yeung, J., Traeger, L., Regalo, G., Gourlay, R., Badiani, S., Koh, C., Putnis, S., Haider, F., Mitul, A. R., Komen, N., Dhondt, B., Cappeliez, S., Pigeolet, M., Schoneveld, M., Stijns, J., Oosterlinck, W., Flamey, N., Kpangon, C., Agbadebo, M., Tobome, S. R., Barros, A. V., Junior, S. A., do Amaral Campos, H. G., Gross, J., Coimbra, F. J. F., Kowalski, L. P., Makdissi, F., Nakagawa, S., Neto, J. P. D., Vartanian, J. G., Yazbek, G., Zequi, S. C., Flumignan, R., Jaworska, N., Dell, A., Shanthanna, H., Behzadi, A., Nessim, C., Mozel, M., St-germain, P., Russell, C., Groot, G., Safieddine, N., Wijeysundera, D., Eskander, A., Chadi, S., Mackenzie, S., Flexman, A., Heredia, F., Villanueva, J., Waissbluth, S., Macchiavello, R., Escudero, M. I., Fuentes, T., Mimica, X., Saenz, D. B., Caicedo, L., Alzate, J. P., Luna, J., Alonso, N. F. P., Silva, C. O., Rodriguez, J., Silva-Igua, L., Torres, M. L., Trujillo, L. M., Calvache, A. J. N., Balanta-Melo, J., Figueroa-Casanova, R., Garcia-Montoya, O. -J., Toro, C. A. M., Botero, M. V., Arango, M. C. M., Martinez, E. D., Perdomo, V. G., Montenegro, E., Rodriguez-Abreu, J., Mejia, D., Abouelnagah, G., Shehata, S., Rida, A. H. E. F., Hassan, R. A., Saad, M. M., Loaloa, M. R., Mostafa, B., Qassem, M., Fahmy, M., Abozied, H., Azzam, A. Y., Ghozy, S., Sallam, A., Shehta, A., Abdelkhalek, M., Samaka, R., Morsy, A., Sherif, A. E., Negussie, A., Fisseha, T., Shumbash, K., Abebe, M., Yasin, S. M., Akililu, Y. B., Megersa, A., Tefera, T., Assefa, M., Atnafu, B., Tsegaye, B., Bezabih, Y. S., Sisay, S., Bekele, K., Jira, M., Derilo, H., Degefa, E., Tadesse, A., Nidaw, M., Sarjanoja, E., Testelin, S., Boucher, S., Jouffret, L., Lakkis, Z., Le Bian, A. Z., Harper, L., des Deserts, M. D., Andre, B., Slim, K., Verhaeghe, R., Police, A., Girard, E., Chebaro, A., Nkembi, A. S., Arnalsteen, L., Ballouhey, Q., Mege, D., Jeandel, C., Duchalais, E., Bouche, P. -A., Manceau, G., Cretolle, C., Hervieux, E., Girard, N., Seguin-Givelet, A., Gaujoux, S., De Simone, B., Boisson, M., Bergeat, D., Fredon, F., Nappi, F., Kassir, R., Scalabre, A., Migliorelli, F., Ezanno, A. -C., Seeliger, B., Vaysse, C., Charbonneau, H., Misrai, V., Abbo, O., Angeles, M. A., Brunaud, L., Modabber, A., Wolf, S., Kamphues, C., Hohn, P., Glowka, T. R., Rokohl, A. C., Bork, U., Fluegen, G., Horch, R. E., Schmedding, A., Schnitzbauer, A., Eberbach, H., Schlager, D., Spelsberg, F., Keppler, L., Hecker, A., Wolfer, S., Ronellenfitsch, U., Nitschke, C., Peiper, C., Hakami, I., Welter, S., Nikolaieva, K., Roth, A., Lindert, J., Gousias, K., Rissmann, A., Linz, V. C., Rahbari, N., Rassweiler-Seyfried, M. -C., Gut, A. E., Gempt, J., Reim, D., Wagner, A., Keppler, A. M., Stoleriu, M. G., Saier, T., Stadler, J., Kaiser, J. C., Brunner, S. M., Pfister, K., Herzberg, J., Nowak, K., Reinhard, T., Stavrou, G. A., Konigsrainer, A., Konrads, C., Quante, M., Laban, S., von Pusch, S., Hirschburger, M., Doerner, J., Wiegering, A., Tampaki, E. C., Ruiz, A. G., Rodas, A., Portilla, A. L., Carrera, J., Duarte, A. B., Lowey, M., Barillas, S., Suroy, A., Vaishnav, D., Chowdappa, R. G., Madabhavi, I., Bhat, D., Venkatappa, S. K., Thakar, S., Jain, K., Kumar, A., Nagar, M., Mishra, T., Sekar, A., Gupta, A., Kaman, L., Karthigeyan, M., Tripathi, M., Rammohan, A., Vayoth, S. O., Rajanbabu, A., Subbian, A., Gupta, R., Raut, M., Evelyn, N., Kannaiyan, R. L., Matai, A., Misra, S., Bhende, V., Muthu, S., Ghosh, I., Sharma, A., Bajaj, A., Rajan, S., Agarwal, G., Pawar, P., Alexander, P., Vijayakumar, M. V., Hameed, Z., Badareesh, L., Chaudhry, N. K., Baliarsing, L., Dharap, S., Kulkarni, A., Thyavihally, Y., Sharma, R. D., Pramesh, C. S., Soni, R., Dube, S. K., Sharma, S., Singh, H., Bains, L., Ghodke, R., Sodhai, V., Maji, S., Basu, S., Mahakalkar, C., Kannan, R., Mehraj, A., Ranganath, N., Phadnis, A., Yadev, I., Kavalakat, A., Mittal, R., Vallam, K. C., Akhavizadegan, H., Maleki, E. R., Kandevani, N. Y., Ikele, H., Mcnestry, C., Fleming, C., O'Brien, S., Elwahab, S. A., Davis, N., Javadpour, M., Mcdonnell, B., Connor, C. O., Bolger, J., Clancy, C., Croghan, S. M., Donlon, N., Cullinane, C., Creavin, B., Muheilan, M., Earley, H., Kabir, S. M. U., Fahadullah, M., Ryan, E., Connelly, T., Hashimoto, D., Alqudah, M. A., Alajalen, A., Omari, R. Y., Qasem, A., Alawneh, Y., Ahmad, A., Aladawi, O., Alrayes, B., Haidar, H., Husain, S., Qassem, F., Sumadi, A., Salhiyeh, A. A., Al-Manaseer, B. M., Alsunna, Z., Ra'Ed, H., Hamad, F. R. B., Abuleil, A., Jimaale, E. A. M., Abu-Mehsen, M., Olaywah, N., Wafi, O., Ababneh, H., Abu-Ismail, L., Khamees, A., Alkhatib, A., Bolatbekova, R., Kulimbet, M., Nurgozhin, T., Saliev, T., Zhussupov, B., Almabayev, Y., Kaidarova, D., Tamoos, K., Aqeelah, A., Mohammed, A. A. K., Al Maadany, F., Alkadeeki, G., Gahwagi, M., Aldressi, W., Amnaina, M., Alansari, A. H. A., Alkaseek, A., Yagoub, G., Amer, A. B., Salem, M., Almugaddami, A., Burgan, D., Abdelkabir, M., Alshareef, K., al Islam Ben Jouira, R., Meelad, A., Bouhuwaish, A., Dwaga, S. E., Khalifa, H., Almiqlash, B., Suliaman, T., Alawami, M., Elhajdawe, F., Aboazamazem, H., Ellojli, I., Msherghi, A., Saleh, I. A., Alayan, M., Ndayishyigikiye, M. D., Munyika, A., Plarre, P., Borowski, D. W., Wells, C., Teague, R., Elliott, B., Kieser, D., Mohyieldin, O., Mcintosh, N., Haran, C., King, J., Ha, J., Mcguinness, M. J., Adesanya, O., Olaogun, J., Akinmade, A., Bwala, K., Agbonrofo, P., Afolabi, A., Usang, U., Ekenze, S., Olori, S., Lawal, T. A., Okunlola, A., Kache, S., Sale, D., Anyanwu, L. -J., Okereke, C., Tolani, M. A., Filipce, V., Todorovic, L., Stavridis, S., Massoud, J. G., Alsibai, S., Sultan, R., Altaf, H. N., Bhatti, A. B. H., Waqar, S. H., Aziz, A., Kerawala, A. A., Rai, L., Anwer, M., Tariq, A., Ayub, B., Niazi, S. U., Naseem, M. Y., Sarwar, M. Z., Khokhar, M. I., Zahid, I. A., Majid, H. J., Talat, N., Asif, M., Chaudhary, M. H., Farooq, U., Ahmad, S., Mabood, W., Bukhari, S. I., Tariq, M., Yaqoob, E., Javed, S., Malik, M. U., Yaqoob, H. N., Pacheco, G. M. F., Melendez, R. M., Urbina, A. D. P. P., Chiuyari, J. R., Alvarado, C. E. O., Lau, L. F. R., Borda-Luque, G., Niquen-Jimenez, M., Arias, C., Zegarra, S., Pallardel, J. B., Oscco, R. A. U., Mendiola, G., Colmenares, Y. T. C., Zapata, C. S., Ortiz, M. R., Borges, F. C., Viveiros, O., Serralheiro, P., Santos-Costa, P., Mendes, F., Melo, M. R., Cardoso, P., Soares, A., Pereira, R. G., Silva, N., Caiado, A., Sacras, M. L., Azevedo, P., Almeida-Reis, R., Oliveira, J., Nogueiro, J., Sampaio-Alves, M., Costa, L. C., Baia, C., Deus, A. C., Branquinho, R., Marcal, A., Tojal, A., Makkai-Popa, S. T., Mironescu, A., Grama, F., Toma, E. A., Filipescu, D., Bacalbasa, N., Motas, N., Ionescu, S., Ginghina, O., Costea, R., Zarnescu, N. O., Drasovean, R., Dimofte, M. -G., Porumb, V., Kirov, M., Molitvin, Y., Pykhteev, V., Raevskaya, M., Butyrskii, A., Alshahrani, M., Althumairi, A., Alzerwi, N., Al Ameer, A., Madkhali, T., Almulhim, A. S., Ghazwani, S., Ayoub, A., Iskander, O., Ghunaim, M., Alharthi, M., Alzaidi, T. M., Alyami, M., Al Amri, A., Alfakhri, A., Alhefdhi, A., Chowdhury, S., Nouh, T., Alshehri, A., Alzahrani, A., Alalawi, Y., Awad, S., Konate, I., Tendeng, J., Teo, N. Z., Aqil, S., Lopez, C. B., Mozo, A. S., Infante, A. R., Vivancos, P. C., Prieto, M., Roman, I. A. S., Fernandez, L. G., Vives, J. M. M., Carreras-Castaner, A., Diaz-Feijoo, B., Sieira-Gil, R., Turrado-Rodriguez, V., Lopez, A. S., Sanchez-Cabus, S., Toscano, M. J., Sin, M. C., Laura, S. G., Sole, O. M., Bellver, P. P., Perez-Bertolez, S., Prat-Ortells, J., Martinez, M. R., Rubio-Palau, J., Tarrado, X., Mendoza, V. A., Bescos, C., Espin-Basany, E., Espinosa-Bravo, M., Gil-Sala, D., Gonzalez-Suarez, S., Estruch, N. M., Marino, L. P., Rodriguez-Tesouro, A., Portilla, F. R., Perez, M. P. T., Vives, I., De Cortazar, U. G., Tudela, K., Landaluce-Olavarria, A., Gomez, M. E., Almoguera, J., Ugarte-Sierra, B., Jimenez, V., Bertrand, M., Puiggros, L. C., Delisau-Puig, O., Garcia-Adam ez, J., Bergkvist, D. J., Maldonado-Marcos, E., Garcia, L. D., Golet, M. R., Soto-Darias, I., Rahy-Martin, A. C., Enjuto, D., Ramos-Luengo, A., Fernandez, J. D., Duarte, C. L., Thies, C. O., Marquez, L., Vita, D. C., Dziakova, J., Velasco, J. C., Mateo-Sierra, O., Quintana-Villamandos, B., Valcarcel, C. R., Rio, J., de Leon, L. R. G., Di Martino, M., Prada, J., Gonzalez, J. S., Losada, M., Gomez, J. T. C., Corripio-Sanchez, R., Forero-Torres, A., Morales-Puebla, J. M., Perez-Chrzanowska, H., Gonzalez, S. V., Yebes, A., Zapardiel, I., Alonso, M. D., Palacios, N. M., Sanchez, A. C., Fernandez, F. S., Gurumeta, A. A., Abad-Motos, A., Corella, F., Ripolles-Melchor, J., Sanz-Gonzalez, R., Fuentes, M. A., Martin, M. T. F., Espino, P. C., Prats, M. C., Fernandez-Lopez, A. -J., Escudero, D. G., Soria, V. G., Alonso, J. A. M., Ruiz-Marin, M., Perez, B. G., Moya-Angeler, J., Martinez, D. F., Bayo, H. L., Colas-Ruiz, E., Romera, S. B., Pellice, M. T. G., Sole, M. J., Velasquez, E. J. R., Nunez, B., Jimenez, R., Zabaleta, J., Gonzalez-Gimeno, M. J., Vazquez, I. O., Ferrer, A. P., Martin-Laez, R., Suarez, M. M., Eiras, M. A. F., Ramallo-Solis, I., Gomez-Rosado, J. -C., Guillen, J. R. O., Boira, M. A., Bauset, J. C. C., Domenech, J., Badenes, R., Bernal-Sprekelsen, J. C., Sancho-Muriel, J., De Andres-Asenjo, B., Tejero-Pintor, F. J., Vallve-Bernal, M., Melero, A. V., Blasco, L. S., Escartin, J., Mallen, V. D., Srishankar, S., Sooriyabandara, C., Basnayake, O., Gunawansa, N., Weeraddana, P. D., Vimalakanthan, T., Gishanthan, S., Chandrasinghe, P., Sauvain, M. -O., Ghazal, A., Al-Sabbagh, Y., Alhassoun, T., Albared, S. M., Naem, A., Alnahr, H., Jisry, G., Hammed, A., Xaviour, O. F., Turinawe, G., Mubezi, I., Sikakulya, F. K., Kakeeto, A., Kabweru, W. M., Kiweewa, R., Matovu, P., Isaac, O., Mashhour, M., El Helw, A., Kherani, S., Mohamed, A., Abbas, F. M. A., Mohammed, D., Aldlyami, E., Kundra, R., Michael, A. L. R., Khalil, K. 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H., Datler, P., Dawoud, C., Farr, A., Foessleitner, P., Grimm, C., Harpain, F., Hoda, M. A., Holawe, S., Kranawetter, M., Ott, J., Perricos, A., Pesta, M., Pillerstorff, R., Reiterer, C., Riss, S., Rosta, K., Scheriau, G., Tschernko, E., Wenzl, R., Wiedemann, D., Wohlrab, P., Zapletal, B., Zimmermann, M., Zimpfer, D., Findl, O., Fisus, A., Ruiss, M., Komaz, M., Meindl, N., Primavesi, F., Stadlbauer, K. H., Stattner, S., Steiner, F., Cerny, O., Falkensammer, E., Knotzer, H., Koglberger, P., Poidinger, B., Wiesinger, C. G., Burtscher, J., Rath, S., Trivik-Barrientos, F., Aliyeva, G., Behbudov, V., Muslumov, G., Zeynalov, N., Alam, M., Alfayez, F., Hasan, B., Mahdi, M., Mulla, H., Qader, K., Saeed, A., Shirazi, A., Albastaki, A., Birido, N., Chagla, H. H., Dawaishan, A., Dawaishan, B., Farhan, A., Juma, I., Khan, A., Patel, A. M. E., Srinivasan, M., Deen, F. W. A. M. A. N., Abdulqadir, S., Jabr, A., Maqsood, F., Almoosa, N., Naseer, M., Alam, M. S., Basher, A. K. M. K., Islam, S. M. N., Karim, S., Faisel, M., Khan, S., Mannan, I. I., Nazia, N., Bentham, M., Corbin, S., Doyle, A., Eastmond, A., Haynes, A., O'Shea, M., Phillips, E., Walkes, K., Artyushkov, E. L., Kaplan, M. L., Straltsov, V., Litvina, Y., Lyzikov, A., Tihmanovich, V. E., Borges, M., Brits, T., De Hous, N., De Wachter, S., Menovsky, T., Mortiers, X., Vermeulen, D., Vleminckx, N., Ysebaert, D., Bontinck, J., Bulthe, D., Rasschaert, R., Van Haver, A. -S., Van Belle, K., Verstraeten, L., Vounckx, M., D'Ulisse, S., De Bruyne, Y., El Nakadi, B., Heloise, T., Luisetto, M., Marinakis, S., Maton, M., Viste, C., Van Daele, E., Vandeputte, M., Duinslaeger, M., Jacobs-Tulleneers-Thevissen, D., Jansen, Y., Janssens, W., Kunda, R., Messaoudi, N., Ruyssers, M., Van Eetvelde, E., Vanhoeij, M., Van den Eynde, J., Van den Eynde, R., Chaoui, A. M., Akpla, M., Lawani, S., Agossou, H., Behanzin, H. A., Bokossa, C., Dewanon, H., Yome, H., Boukari, A., Gbehade, O., Amossou, L. 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H., Kamel, M., Khallaf, M., Elghazaly, S. M., Mahfouz, A., Mahmoud, O., Mahran, W., Mahrous, D., Marsis, A., Hussein, A. M., Sayed, A. M., Mohammed, M. M., Mokhtar, A., Monib, F. A., Nageeb, A., Nageh, M. A., Nageh, M., Omar, N. G., Ragab, A., Ramadan, A., Temerik, A. R., Safwat, H., Salah, O., Mahmoud, A. E. S., Saleh, A., Sallam, M., Samir, A., Sayad, R., Sayed, E., Sedik, A. S., Shahine, M., Soliman, A., Soliman, W., Taher, M. G., Wanees, R., Yousof, E. A., Youssef, A., Elabedeen, O. Z., Hassan, A. E. S., Fattah, S. A., Abostate, A., Ali, S., Salama, S. A. S., Allam, M., Alsadek, A., Arafa, E., Barakat, A., El Sherpiny, M., Elbehairy, G., Eleisawy, M., Elgendy, A., Elhawary, R., Eltregy, S., Hamdy, M., Hassan, G., Khalifa, A., Mahmoud, A., Altukhy, A. M., Noah, K., Noureldin, Y., Nowar, M., Saad, M., Elsaeidy, A. S., Elsaeidy, K. S., Sabry, H., Sameh, M., Said-elnaby, A. T., Zahed, M., Zahran, M., Zaid, A., Zoghary, A. Z., Atef, M., Abdelhamid, M. H. S., Alazab, E., Awad, A. K., Darwesh, A., El Fiky, L., Elgarhy, I., Nassef, M. A., Shaban, M., Shalaby, M. M. M., Wahba, A., Fouad, O. Y. O., Elsadek, M., Gad, D., Abdelsamed, A., Bayomy, A., Elsalhy, M., Fahim, A., Seleim, A., Afifi, E., Gamal, F. A., Gamal, M., Eldesouky, O., Eldwini, M. H. E. E., Fahmy, M. M. F., Hussein, A., Ouf, A., Sami, O., Shaat, S., Bahi, A. W. M. K., Atea, A., Gamal, I., El Kassas, M., Omar, W., Tawheed, A., Al-oribi, S., Aly, N. K., Elfiky, M., Elmaghraby, A. E., Elrahmany, A., Elsherbeeny, M., Helmy, Y., Nabil, A., Farahat, A. S., Soliman, M., Wassef, A., Abdelrahman, A., Elsaban, S., Ghaly, G., Hamdy, R., Mondy, H., Abdallah, L., Darwish, A. K. Z., Rabea, M., Azab, M. A., Abbas, A. S., El-Deeb, M., Fawzy, M., Ibraheem, M., Bakry, A., Elnems, S., Elsheikh, R., Gbreel, M. I., Hafez, M., Jammal, M., Hamam, K. M., Makram, A. M., Makram, O. M., Rabie, S., Askalany, S. Y., Abushanab, M. M. I., Eid, A., El Ghalid, M. R. I. A., Abdelaty, A. A., Fayad, E. A., Radwan, A., Shokry, A., Farouk, A. M., Elfallal, A., Elfeki, H., Elsaeed, M., Elsaid, M., Makroum, A., Elsaid, D. M., Mostafa, M., Omar, M. W., Rezk, M., Sakr, A., Sanad, A., Shalaby, M., Shawqy, M., Shetiwy, M., Shoma, A., Tawakl, N., Yunes, A., Abouzid, A., Atallah, K., Elmorsi, R., Elsherbini, A., Gaballa, K., Hamdy, O., Metwally, I. H., Refky, B., Zuhdy, M., Zahran, M. A., Abdellah, F., Abdelmawla, A., Abdrabou, A., Abubakr, A., Al Gohary, R., Al-Shazly, M. H., Allam, A. R., Aposaeeda, A., Asfour, M., Ayman, A., Omran, A. A., Daghash, I. T., Ebada, M. A., Eid, T., El Kelany, A., El Shemy, E., El-Hag-Aly, M., Elgamal, O., Elghoury, M., Elkased, A. F., Ellakwa, T. H., Ellakwa, H., Elmeanawy, A., Elnoamany, S., Elsabagh, A., Elsawey, A., Elshabrawy, E., Elshakhs, S., Elsoudy, N., Ezzat, E., Fawzy, A., Gamal, A., Gameel, A., Gharbia, K., Ghonaim, M., Ghonaim, A., Hafez, A., Ismail, Z., Khaled, M., Meselhy, M., Mikhail, P., Mougahed, M., Mustafa, A., Nada, A., Omran, J., Ebiad, M. S., Saleh, I., Salem, N., Salem, O., Selim, S., Shalaby, G., Sherif, H., Soltan, H., Wahbah, M., Abdelbary, E. Z., Zayan, A. H., Afify, A., Hadiya, H. A., Elshref, M. J., Ahmed, M. M., Nasser, N., Abdeldayem, H., Salama, I. A., Ammar, K., Ayoub, I., Badawy, M. T., Balabel, M., Fayed, Y., Gad, E. H., Gomaha, M., Hammad, E., Hegazy, O., Hegazy, E., Ibrahim, T., Kallaf, M., Macshut, M., Magdy, A., Oteem, A., Samaan, S., Sharshar, M., Shoreem, H., Soliman, E., Soliman, H. E., Yassein, T., Zakaria, H., Eldaly, A., Mashaly, S., Abd-Elsalam, S., Abdel-Elsalam, W., Shaalah, A. A., Elbahnasawy, M., Elhalaby, I., Hamada, M., Soliman, S. H., Hawila, A., Morsy, M. S., Naieem, M., Nasreddin, M., Salman, S., Sarsik, S., Shabana, A., Tolba, E., Zagho, M., Kams, L., Ratsep, T., Riips, K., Abdurehman, O., Admasu, A., Berhea, A., Eado, Y., Hailu, N., Kidane, M., Mohammed, A., Mohammed, K., Tibelt, A., Woldemariam, M. A., Yonael, L., Alemu, M., Aklilu, A. T., Asele, F., Assefa, S., Azmach, D., Bekele, P., Mamo, M., Maru, N., Mekuria, H., Menkir, A., Mikru, F., Siraw, E., Suga, H., Sumoro, N., Teka, A., Thomas, E., Woldemariam, D., Wubishet, E., Abebe, E., Abebe, K., Asfaw, F., Bergene, E., Eshete, M., Gebrehiwot, F. G., Gedefaw, Y., Mengesha, M. W., Mengiste, N., Menjeta, A., Muleta, M. B., Sefera, S., Tedla, Y., Teklu, D., Teshome, H., Tirfe, L., Tsegabrhan, S., Tsehaye, M., Worku, B., Molla, M., Supha, M., Taye, T., Abebe, N., Alemu, B., Chanie, A., Degefu, H., Desalegn, D., Gebre, H., Hussen, H., Kassa, D., Laeke, T., Mammo, T. N., Negash, S., Sahlu, A., Tiruneh, A. G., Wolde, A., Woldeselassie, H. G., Ahmed, M. Y., Zewdneh, B., Fentaw, J., Salia, S., Tabore, K., Gurara, A., Abreha, T., Abrha, T., Beyene, G., Weldu, M. A., Abdissa, D., Tesfaw, M., Wolle, M., Asmamaw, D., Assefa, B. Z., Bedane, D., Bekele, E., Getie, A., Melkamu, S., Mengesha, W., Shumye, G., Tagele, G., Tesfa, A. A., Workneh, W., Genetu, S., Mebratu, E., Chanyalew, L., Deresse, T., Girma, A., Seid, M., Shimelash, D., Shitaw, A., Ayalew, T., Diress, T., Kassahun, B., Kassaye, B., Mulugeta, E., Tesfaw, G., Yimenu, B., Benecha, S., Aman, M., Mekete, A., Tesemma, A., Mohammed, A. A., Abdullahi, Y. Y., Adem, E., Ahmedin, M., Assefa, Y., Ayde, F., Berhe, A., Gebremeskel, Z., Siyoum, E. G., Teresa, S., Wude, Z., Yemer, F., Yohannes, D., Zeleke, E., Zerihun, G., Degefe, D. W., Derilo, H. T., Eliyas, N., Bayissa, F., Deressa, Y., Gemechu, L., Gurmu, T., Kasaye, A., Melese, L., Muleta, L., Mulugeta, G., Taye, S., Teshome, A., Tesso, B., Gebrekirstos, G., Haile, M., Kassa, H., Saddik, M., Mengist, A., Heikkinen, J., Helminen, O., Huhta, H., Kotkavaara, T., Mosorin, M. -A., Pitkanen, J., Qian, C., Sinikumpu, J., Sova, H., Tastula, M., Virta, V. P., Bettoni, J., Dakpe, S., Devauchelle, B., Lavagen, N., Bastard, F., Bin, K., Breheret, R., Fouquet, O., Gueutier, A., Henric, N., Kahn, A., Kun-Darbois, J. -D., Moukoko, D., Pineau, A., Podevin, G., Schmitt, F., Alshawared, F., Beyrne, C. D., Lugans, L., Marie-Macron, L., Doussot, A., Ahmed, O., Alnajjar, L., Mis, T. C., Fliss, S., Giocanti-Auregan, A., Gregory, T., Guiraudet, P., Le Fouler, A., Martinod, E., Onorati, I., Peretti, M., Quilichini, J., Radu, D., Tresallet, T., Andro, C., Maffert, A., Chapman, T., Halden, M., Fayon, J., Mattevi, C., Marion, H., Bendjemar, L., Lionel, C., Mikhael, E., Macias, R. M., Villefranque, V., Volpin, E., Trilling, B., Boleslawski, E., Constance, H. -L., Drubay, V., El Amrani, M., Eveno, C., Lecolle, K., Martin, L., Noiret, B., Piessen, G., Truant, S., Zerbib, P., Aubry, E., Denimal, F., Lamblin, A., Barrat, B., Caire, F., Christou, N., Fourcade, L., Laloze, J., Bouv-Hez, M. M., Salle, H., Taibi, A., Tricard, J., Usseglio, J., Chopinet, S., Gregoire, E., Delpont, M., Blanchard, C., Crenn, V., de Vergie, S., Denis, W., Fragnaud, H., Regenet, N., Rigaud, J., Varenne, Y., Anract, P., Barat, M., Biau, D., Dautry, R., Dohan, A., Idier, L., Lang, E., Thouny, C., Tzedakis, S., Audenet, F., Cazelles, A., Chamouni, A., Karoui, M., Mejean, A., Clermidi, P., Langlais, T., Leonelli, L., Maisonneuve, E., Nicolas, B., Perrot, O., Prost, D., Thomin, A., Thouement, T., Athiel, Y., Berry, R., Boddaert, G., Bonnet, S., Cathala, N., Conso, C., Denet, C., Laforest, A., Levy-Zauberman, Y., Macek, P., Mombet, A., Ollat, D., Scamporlino, A., Zadegan, F., Amine, C. A., Baratte, B., Chartier-Kastler, E., Chereau, N., Colas, P. -A., Duquesne, I., Genser, L., Petit, G. G., Goumard, C., Hasani, A., Lim, C., Martellotto, S., Melot, C., Menegaux, F., Pinar, U., Pocard, M., Roupret, M., Scatton, O., Seisen, T., Severine, N., Turco, C., Chouillard, E., Beganton, P., Frasca, D., Kerforne, T., Corbiere, L., Gasmi, A., Ghemame, M., Guerin, S., Khene, Z. -E., Livin, M., Mahmoud, F., Maillot, B., Merdrignac, A., Mouriaux, F., Robin, F., Sulpice, L., Vazeux, C., Bertheuil, N., Bonneau, S., Cazemajou, C. T., Cousin, I., Defert, C., Fustec, E., Juricic, M., Lavoue, V., Mevel, G., Timoh, K. N., Renault, A., Violas, P., Schwarz, L., Tuech, J. J., Morichau-Beauchant, T., Sauvat, F., Haddad, E., Vermersch, S., Patrizi, A., Roux, A., Aime, A., Malgras, B., Cherkaoui, Z., D'Urso, A., Felli, E., Gonzalez, C. A., Ignat, M., Mutter, D., Pessaux, P., Vix, M., Gornes, H., Vergriete, K., Berthoumieu, P., Genre, L., Le Gall, H., Pierre, T., Chalhoub, M., Del, M., Martinez, A., Fuchs-Buder, T., Vancon, A., Faya, C. A., Asaph, E., Baruwa, E., Hofman, G., Machemedze, S., Idiata, M. M., Muhemi, R., Ndizeye, O., Nkunzimana, E., O'Connor, J., O'Connor, Z., Tchoba, S., Boumas, N., Devidze, G., Pisarevi, G., Baumgarten, S., Grusser, L., Holzle, F., Kowark, P., Kowark, A., Rossaint, R., Schafer, B., Wallqvist, J., Winnand, P., Ziemann, S., Anthuber, M., Broecheler, T., Edlinger, F., Gosslau, Y., Hyhlik-Duerr, A., Maksymiw, F., Shiban, E., Sommer, F., Sommer, B., Zerwes, S., Beyer, K., Lauscher, J. C., Lee, L. D., Loch, F. N., Schineis, C., Aghalarov, I., Belyaev, O., Braumann, C., Enste, A., Fahlbusch, T., Herzog, T., Horn, J., Jedanowski, J., Knipschild, J., Luu, A. M., Mohan, P. V., Siemen, L., Slobodkin, I., Strotmann, J. J., Uhl, W., Wolf, K., Coburn, M., Egger, E., Eichhorn, K., Enderes, J., Far, F., Franzen, A., Guresir, E., Hadjiathanasiou, A., Kalff, J. C., Kohistani, Z., Manekeller, S., Mustea, A., Probst, C., Randau, T., Recker, F., Schuss, P., Strassberger-Nerschbach, N., Strieth, S., Treede, H., van Beekum, C. J., Vatter, H., Velten, M., Vilz, T. O., Wirtz, D., Wittmann, M., Behr, M., Bulian, D. R., Marche, B., Moczko, T., Otchwemah, R., Schulz, S. -A., Thomaidis, P., Bruns, C., Cursiefen, C., Domrose, C., Fuchs, H., Heindl, L. M., Mallmann, M. R., Mallmann, C., Ratiu, D. A., Canzler, U., Distler, M., Korn, S., Meisel, C., Meusel, M., Petzold, A., Praetorius, C., von Renesse, J., Weitz, J., Wimberger, P., Alkhanji, N., Fung, S., Jaber, K., Knoefel, W. T., Vay, C., Clonda, O., Cottin, T., Juodiene, E., Juodis, D., Petrovic, B., Solodarenko, O., Binder, J., Grutzmann, R., Hackner, D., Junker, S., Arsalan, M., Banek, S., Chun, F., Faqar-Uz-Zaman, S. F., Keese, D., Kluth, L., Rolle, U., Van Linden, A., Walther, T., Bayer, J., Beck, J., Fung, C., Kraus, L. M., Leiber, C., Neidert, N., Sandkamp, R., Schnell, O., Schulte, A., Strahle, J., Jarmusch, S., Novotny, H. F. G., Becker, J., Fulghum, C., Gonschor, B., Herbolzheimer, M., Nicolaiciuc, S., Trulson, A., Vogelsang, H., Zimmermann, B., Akbari, A. A., Boening, A., Edinger, F., Hecker, M., Knitschke, M., Koch, C., Reichert, M., Schmidt, G., Schneck, E., Uhl, E., Nobrega, S. F., Kauffmann, P., Miller, C., Nemeth, M., Sievers, D., Kisser, U., Kleeff, J., Klose, J., Lorenz, K., Papendick, N., Plontke, S., Seiwerth, I., Steer, S., Thomssen, C., Ukkat, J., Dumpies, C. W., Gessner, M., Hanke, J., Klauke, F., Leuschner, S., Mendel, T., Muller, K., Schmidt, B., Schreiter, V., Stosberg, P., Vinz, F., Herbig, B., Sander, J., Schulte, T. M., Betz, C. S., Bewarder, J., Bier, J., Bottcher, A., Burg, S., Busch, C. -J., Bussmann, L., Gosau, M., Heuer, A., Izbicki, J., Klatte, T. O., Konig, D., Kopke, L. -G., Moeckelmann, N., Praetorius, M., Priemel, M., Stadlhofer, R., Stangenberg, M., Uzunoglu, F. G., Wittig, L., Zech, H., Zeller, N., Roux, F., Spaeth, T., Fricker, R., Muller, T., Schroder, L., Alasmari, M., Boeker, C., Hakami, I. A., Mall, J. W., Kyritsis, I., Graeb, C., Huber-Strossner, K., Branzan, D., Doss, M., Gockel, I., Jodicke, C., Osterhoff, G., Pempe, C., Sucher, R., Adler, T., Kelly, K., Merkle, J., Siebert, J., Hirche, C., Kneser, U., Tapking, C., Agrawal, R., Qureischie, H., Croner, R., Koslowski, L., Krause, H., Meyer, F., Turial, S., Al-Nawas, B., Battista, M. J., Goedeke, J., Hasenburg, A., Heider, J., Mueller, L. K., Zeller, S., Jentschura, S. L. P., Kowalewski, K. -F., Kriegmair, M., Mannle, D., Reissfelder, C., Rotter, N., Scherl, C., Seyfried, S., Kirschniak, A., Rolinger, J., Wilhelm, P., Bader, F. G., Ottl, S., Behr, A. V., Diamantis, A., Fichter, A., Grill, F., Heck, M., Jira, D., Kallmayer, M., Koll, F., Luhne, S., Meyer, B., Patachia, R., Pergolini, I., Safi, S., Schaffer, C., Schirren, M., Wegmann, H., Wirth, M., Zhu, Z., Aghamaliyev, U., Almaghrabi, M., Bocker, W., Bruder, J., Frank, K., Herterich, V., Huber, V., Ilmer, M., Kammerlander, C., Neuerburg, C., von Ehrlich-Treuenstatt, V. H., Werner, J., Borner, N., Fegg, F., Hartmann, D., Ladurner, R., Liokatis, P., Patzer, K., Schlager, J. G., Smolka, W., Zimmermann, P., Hatz, R., Steinhart, D., Glowalla, C., Schneidmueller, D., Henkel, K. W., Steiner, M., Holz, K., Knorr, C., Kuehlmann, B., Oikonomou, K., Prantl, L., Flurschutz, R., Honarpisheh, H., Kroger, M., Lepiorz, D., Luths, C., Niemeier, A., Sras, Y., Strate, T., Winter, T., Freiman, T., Gessler, F., Won, S. -Y., Widyaningsih, R., Hoffmann, S., Schafer, R. C., Thiel, J. T., Bertolani, E., Steidle, C., Uberruck, L., Yurttas, C., Ziegler, P., Zimmermann, A., Bolenz, C., Dayan, D., Greve, J., Hoffmann, T. K., Janni, W., Lobig, N., Schochter, F., Vahl, J. M., Wezel, F., Greif, V., Schmidbauer, S., Marsch, I., Schneider, R., Boenicke, L., Degener, S., Dreger, N. M., Horstmeier, F. C., Kruschwitz, J., Rombach, A., Schmidt, N., Seiberth, R., Singh, J., Smit, M., von Rundstedt, F. -C., Zirngibl, H., Diessner, J., Friedrich, S., Germer, C. -T., Helmer, P., Herrmann, J., Kranke, P., Kubler, H., Lock, J., Lotz, C., Meffert, R., Meybohm, P., Muller, S., Notz, Q., Popp, M., Schlegel, N., Schlesinger, T., Schmid, B., Sitter, M., Steinisch, A., Treutlein, A., van den Berg, A., Wurmb, T. E., Agyeman-Duah, N. K., Appiah, E., Armah, R., Asare, C., Awere-Kyere, L., Daary, D., Gakpetor, D., Allah, S. M., Obbeng, A., Osei-Poku, D., Puozaa, D., Tackie, E., Adu-Aryee, N. A., Agboadoh, N., Asare, O., Bowan, A. B., Brown, G. D., Clegg-Lamptey, J. -N., Dedey, F., Dery, C., Fenu, B. S., Harrison, M. A., Kumassah, P., Kuuzie, E., Nsaful, J., Olayiwola, D. O., Smith, C., Banka, C., Hussey, R., Azize, D. A., Aniakwo, L. A., Adofo-Asamoah, Y., Agbeno, E. K., Agyapong, M. M., Agyen, T., Mensah, K. A., Alhassan, B. A. B., Amoako-Boateng, M., Appiah-Thompson, P., Gyimah, N. A. -M., Asante-Bremang, M., Asante-Asamani, A., Atawurah, H., Appiah, A. B., Baidoo, R. O., Baidoo, E. I., Boakye, B., Boateng, A., Dadoe, D., Dayie, M. S. C. -J. K., Debrah, S., Doku, K., Enti, E., Ken-Amoah, S., Koggoh, P., Kpangkpari, R., Maison, P., Mensah, S., Mensah, P., Mensah, T. A., Morna, M. T., Nimako-Mensah, J., Nkrumah, J., Nortey, M., Ofori, E. O., Opandoh, I. N. M., Osei-Tutu, E., Adae, J. O., Quansah, K., Quartson, E., Rahman, G. A., Walawah, D., Yigah, M., Yussif, S., Jiagge, N., Nachelleh, E., Acquaye, J., Agbedinu, K., Agyei, F., Agyemang-Prempeh, A., Amo-Antwi, K., Amoah, M., Amoah, G., Amoako, Y. A., Aning, D. G., Ankobea-Kokroe, F., Mintah, D. A., Anyitey-Kokor, D., Appiah-kubi, A., Arthur, J., Ativor, V., Barnor, I., Braimah, Y., Darko-Asante, R., Davor, A., Issahalq, M. D., Dzogbefia, M., Emile, T., Fiifi-Yankson, P., Gaveh, V., Gudugbe, S., Gyabaah, S., Gyamfi, F. E., Gyedu, A., Gyimah, D., Hammond, B., Jonathan, B. -Y., Joseph, Y., Konney, T. O., Konney, A., Kusi, K., Kyei, I., Lovi, A., Naabo, N., Nimako, B., Nyadu, B., Nyarko, O. O., Ofosu-Barko, B. B., Oppong, P. P., Osabutey, A., Poku, M., Sagoe, R., Yifieyeh, A., Ansong, G., Abass, A., Abdul-Mumin, A., Adjeso, T., Alatiiga, J. A., Amadu, M., Annan, N., Leal, G. A., Bukari, M., Buunaaim, A., Cheyuo, E., Salifu, L. D., Damah, M., Dery, M., Dzantor, E. K., Garcia, O. G., Baba, Y. I., Issaka, A., Muntaka, A. -J. M., Murphy, J., Agyeman, Y. N., Amankwaa, W. O., Osman, I., Pie, S., Seidu, A. S., Sheriff, M., Charadan, A. M. S., Titigah, A., Yahaya, M., Yakubu, M., Yenli, E. M. T. -A., Grypiotis, I., Kiriakopoulos, N., Koliopoulos, G., Kyvelos, V., Micha, G., Papadopoulou, T., Balalis, D., Fradelos, E., Korkolis, D., Alexakis, N., Angelou, K., Haidopoulos, D., Prodromidou, A., Rodolakis, A., Thomakos, N., Psychogios, D., Antonakis, P., Bramis, K., Chardalias, L., Contis, I., Dafnios, N., Dellaportas, D., Dimitra, P., Fragkoulidis, G., Gkiokas, G., Gklavas, A., Hadjizacharias, T., Karageorgou, D., Konstadoulakis, M., Kontopoulou, C., Massaras, D., Memos, N., Papaconstantinou, I., Politis, D., Polydorou, A., Stamatis, K., Theodosopoulos, T., Vezakis, A., Avgerinos, K., Katunin, J., Kechagias, A., Kelgiorgi, D., Kritikos, N., Pengerma, P., Bisdas, T., Ioannidis, A., Konstantinidis, M., Konstantinidou, S., Patelis, N., Antonopoulou, M. I., Deskou, E., Kalles, V., Manatakis, D. K., Stamos, N., Tasis, N., Arkadopoulos, N., Danias, N., Economopoulou, P., Frountzas, M., Kokoropoulos, P., Michalopoulos, N., Selmani, J., Sidiropoulos, T., Vassiliu, P., Paraskevas, K. 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H., Kamel, M., Khallaf, M., Elghazaly, S. M., Mahfouz, A., Mahmoud, O., Mahran, W., Mahrous, D., Marsis, A., Hussein, A. M., Sayed, A. M., Mohammed, M. M., Mokhtar, A., Monib, F. A., Nageeb, A., Nageh, M. A., Nageh, M., Omar, N. G., Ragab, A., Ramadan, A., Temerik, A. R., Safwat, H., Salah, O., Mahmoud, A. E. S., Saleh, A., Sallam, M., Samir, A., Sayad, R., Sayed, E., Sedik, A. S., Shahine, M., Soliman, A., Soliman, W., Taher, M. G., Wanees, R., Yousof, E. A., Youssef, A., Elabedeen, O. Z., Hassan, A. E. S., Fattah, S. A., Abostate, A., Ali, S., Salama, S. A. S., Allam, M., Alsadek, A., Arafa, E., Barakat, A., El Sherpiny, M., Elbehairy, G., Eleisawy, M., Elgendy, A., Elhawary, R., Eltregy, S., Hamdy, M., Hassan, G., Khalifa, A., Mahmoud, A., Altukhy, A. M., Noah, K., Noureldin, Y., Nowar, M., Saad, M., Elsaeidy, A. S., Elsaeidy, K. S., Sabry, H., Sameh, M., Said-elnaby, A. T., Zahed, M., Zahran, M., Zaid, A., Zoghary, A. Z., Atef, M., Abdelhamid, M. H. S., Alazab, E., Awad, A. 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A., Radwan, A., Shokry, A., Farouk, A. M., Elfallal, A., Elfeki, H., Elsaeed, M., Elsaid, M., Makroum, A., Elsaid, D. M., Mostafa, M., Omar, M. W., Rezk, M., Sakr, A., Sanad, A., Shalaby, M., Shawqy, M., Shetiwy, M., Shoma, A., Tawakl, N., Yunes, A., Abouzid, A., Atallah, K., Elmorsi, R., Elsherbini, A., Gaballa, K., Hamdy, O., Metwally, I. H., Refky, B., Zuhdy, M., Zahran, M. A., Abdellah, F., Abdelmawla, A., Abdrabou, A., Abubakr, A., Al Gohary, R., Al-Shazly, M. H., Allam, A. R., Aposaeeda, A., Asfour, M., Ayman, A., Omran, A. A., Daghash, I. T., Ebada, M. A., Eid, T., El Kelany, A., El Shemy, E., El-Hag-Aly, M., Elgamal, O., Elghoury, M., Elkased, A. F., Ellakwa, T. H., Ellakwa, H., Elmeanawy, A., Elnoamany, S., Elsabagh, A., Elsawey, A., Elshabrawy, E., Elshakhs, S., Elsoudy, N., Ezzat, E., Fawzy, A., Gamal, A., Gameel, A., Gharbia, K., Ghonaim, M., Ghonaim, A., Hafez, A., Ismail, Z., Khaled, M., Meselhy, M., Mikhail, P., Mougahed, M., Mustafa, A., Nada, A., Omran, J., Ebiad, M. S., Saleh, I., Salem, N., Salem, O., Selim, S., Shalaby, G., Sherif, H., Soltan, H., Wahbah, M., Abdelbary, E. Z., Zayan, A. H., Afify, A., Hadiya, H. A., Elshref, M. J., Ahmed, M. M., Nasser, N., Abdeldayem, H., Salama, I. A., Ammar, K., Ayoub, I., Badawy, M. T., Balabel, M., Fayed, Y., Gad, E. H., Gomaha, M., Hammad, E., Hegazy, O., Hegazy, E., Ibrahim, T., Kallaf, M., Macshut, M., Magdy, A., Oteem, A., Samaan, S., Sharshar, M., Shoreem, H., Soliman, E., Soliman, H. E., Yassein, T., Zakaria, H., Eldaly, A., Mashaly, S., Abd-Elsalam, S., Abdel-Elsalam, W., Shaalah, A. A., Elbahnasawy, M., Elhalaby, I., Hamada, M., Soliman, S. H., Hawila, A., Morsy, M. S., Naieem, M., Nasreddin, M., Salman, S., Sarsik, S., Shabana, A., Tolba, E., Zagho, M., Kams, L., Ratsep, T., Riips, K., Abdurehman, O., Admasu, A., Berhea, A., Eado, Y., Hailu, N., Kidane, M., Mohammed, A., Mohammed, K., Tibelt, A., Woldemariam, M. A., Yonael, L., Alemu, M., Aklilu, A. 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A., Workneh, W., Genetu, S., Mebratu, E., Chanyalew, L., Deresse, T., Girma, A., Seid, M., Shimelash, D., Shitaw, A., Ayalew, T., Diress, T., Kassahun, B., Kassaye, B., Mulugeta, E., Tesfaw, G., Yimenu, B., Benecha, S., Aman, M., Mekete, A., Tesemma, A., Mohammed, A. A., Abdullahi, Y. Y., Adem, E., Ahmedin, M., Assefa, Y., Ayde, F., Berhe, A., Gebremeskel, Z., Siyoum, E. G., Teresa, S., Wude, Z., Yemer, F., Yohannes, D., Zeleke, E., Zerihun, G., Degefe, D. W., Derilo, H. T., Eliyas, N., Bayissa, F., Deressa, Y., Gemechu, L., Gurmu, T., Kasaye, A., Melese, L., Muleta, L., Mulugeta, G., Taye, S., Teshome, A., Tesso, B., Gebrekirstos, G., Haile, M., Kassa, H., Saddik, M., Mengist, A., Heikkinen, J., Helminen, O., Huhta, H., Kotkavaara, T., Mosorin, M. -A., Pitkanen, J., Qian, C., Sinikumpu, J., Sova, H., Tastula, M., Virta, V. 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M., Salle, H., Taibi, A., Tricard, J., Usseglio, J., Chopinet, S., Gregoire, E., Delpont, M., Blanchard, C., Crenn, V., de Vergie, S., Denis, W., Fragnaud, H., Regenet, N., Rigaud, J., Varenne, Y., Anract, P., Barat, M., Biau, D., Dautry, R., Dohan, A., Idier, L., Lang, E., Thouny, C., Tzedakis, S., Audenet, F., Cazelles, A., Chamouni, A., Karoui, M., Mejean, A., Clermidi, P., Langlais, T., Leonelli, L., Maisonneuve, E., Nicolas, B., Perrot, O., Prost, D., Thomin, A., Thouement, T., Athiel, Y., Berry, R., Boddaert, G., Bonnet, S., Cathala, N., Conso, C., Denet, C., Laforest, A., Levy-Zauberman, Y., Macek, P., Mombet, A., Ollat, D., Scamporlino, A., Zadegan, F., Amine, C. A., Baratte, B., Chartier-Kastler, E., Chereau, N., Colas, P. -A., Duquesne, I., Genser, L., Petit, G. G., Goumard, C., Hasani, A., Lim, C., Martellotto, S., Melot, C., Menegaux, F., Pinar, U., Pocard, M., Roupret, M., Scatton, O., Seisen, T., Severine, N., Turco, C., Chouillard, E., Beganton, P., Frasca, D., Kerforne, T., Corbiere, L., Gasmi, A., Ghemame, M., Guerin, S., Khene, Z. -E., Livin, M., Mahmoud, F., Maillot, B., Merdrignac, A., Mouriaux, F., Robin, F., Sulpice, L., Vazeux, C., Bertheuil, N., Bonneau, S., Cazemajou, C. T., Cousin, I., Defert, C., Fustec, E., Juricic, M., Lavoue, V., Mevel, G., Timoh, K. N., Renault, A., Violas, P., Schwarz, L., Tuech, J. J., Morichau-Beauchant, T., Sauvat, F., Haddad, E., Vermersch, S., Patrizi, A., Roux, A., Aime, A., Malgras, B., Cherkaoui, Z., D'Urso, A., Felli, E., Gonzalez, C. A., Ignat, M., Mutter, D., Pessaux, P., Vix, M., Gornes, H., Vergriete, K., Berthoumieu, P., Genre, L., Le Gall, H., Pierre, T., Chalhoub, M., Del, M., Martinez, A., Fuchs-Buder, T., Vancon, A., Faya, C. 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H., Antal, Z., Kalman, A., Voros, P., Bahrehmand, K., Echim, T., Novak, Z., Sztipits, T., Bihari, L. A., Hidi, L., Piros, L., Rozsa, B., Sotonyi, P., Szatai, L., Herczeg, G., Pordany, B., Tornyi, F., Dede, K., Egyed, T., Saftics, G., Kulcsicka-Gut, J., Sipos, Z., Toth, D., Patel, B., Majmudar, H., Mankad, S., Pathan, S., Sharathkumarkl, L., Sasatti, L., Mahankali, S., Annayappa, S. K. S., Agrawal, T., Anandan, P., Baindur, A., Bd, M., Savitha, C., Anitha, G. S., Harigond, S., Tejeswini, K. K., Kesarla, V., Manangi, M., Hareesh, P. B., Ranjan, J. K. R., Shetty, A., Chikkanayakanahalli, S. S., Sunil, T., Syamala, S., Tharanath, K., Atal, A., Rajagopal, N., Srinath, B. S., Nk, V., Thirumanikandan, P. L., Mishra, N., Shrivastava, S., Wadhwani, R., Ahmad, R., Haq, Z. A., Behera, P., Dhurwe, R., Haq, R., Jain, V., Karna, S., Pushpalatha, K., Raj, S., Santoshi, J. A., Singh, P., Verma, V., Waindeskar, V., Yadav, M. S., Aziz, Z., Chakraborty, K., Chappity, P., Das, G., Datta, D., Jena, S. K., Kar, M., Khuntia, S., Kumar, P., Kumar, R., Kv, A., Mishra, A., Mishra, S., Mittal, Y., Muduly, D., Panda, R., Panigrahi, S., Parija, S., Patra, S., Rout, B., Sahu, R., Sarkar, S., Singh, S., Sudha, S., Sultania, M., Tripathy, S., Varghese, P., Kansay, R., Kaushik, R., Gupta, S. K., Khare, S., Kumar, V., Mohindra, S., Patil, N., Salunke, P., Savlania, A., Singh, K., Pradeep Krishna, R. V., Narasimhan, G., Rela, M., Appukuttan, A., Goudar, S., Mallick, S., Titus, C., Chidambarasamy, E. S., Madhavan, D., Murugesan, A., Narayanasamy, K., Barani Kumar, P. B., Rajan, F., Vijayaragavan, P., Borthakur, B., Chauhan, T. S., Govil, A., Hanjoora, V. M., Srivastava, A., Tiwari, S., Vishwani, V., Pendyala, K. S., Prasad, N., Bothra, J., Deb, M., Herle, K., Jayaram, H., Kannaiyan, L., Krithiga, A., Mukta, W., Nagpal, P., Pathak, P., Banerjee, S., Chaudhary, R., Choudhary, G. R., Chugh, A., Dixit, P., Elhence, A., Gahlot, N., Garg, M., Ghuman, N. K., Jha, D., Kala, P., Kaur, A., Madduri, V., Pandey, H., Pareek, P., Pathak, M., Rathod, K. J., Rodha, M. S., Saxena, R., Sharma, N., Shekhar, S., Singh, M., Suryanarayanan, B., Vishnoi, J. R., Amin, S., Sharma, T., Murugesan, K., Ramasamy, A. B. S., Chatterjee, D., Gerber, C. G., Naskar, U., Aggarwal, G., Agrawal, S. K., Jain, P., Jain, D., Kewlani, V., Pipara, A., Priya, N., Raja, R., Shakya, S., Thambudorai, R., Kharkongor, D., Akhtar, N., Anand, A., Asnani, M., Chaturvedi, A., Chaurasia, A., Enny, L. E., Garg, S., Jaiswal, A. K., Jaiswal, S., Jaware, Y., Kala, N., Karnatak, R., Kumar, U., Shrivastava, A. K., Mehrotra, S., Mishra, B., Namrata, Ojha, B. K., Ozair, A., Pal, U. S., Pandey, A., Raja, N., Ramakant, P., Roy, A., Sachan, R., Sankhwar, S., Sankhwar, P., Sarin, D., Shukla, A., Singh, K. R., Singh, R., Singh, U., Solanki, V., Sonkar, A. A., Srivastava, C., Suryawanshi, P., Tewarson, V., Verma, R., Verma, M. L., Yadav, A., Chand, G., Chanthar, K. M. M. V., Hoysal, D., Batra, N., Bhatti, A., Chopra, R., David, S., Dhar, T., Dutt, U. K., Dutta, R., Gandhi, S., Haque, P. D., Paul Sudhakar John, B., Veetil, S. K., Kaur, G., Kumar, N., Luther, A., Mahajan, A., Mandrelle, K., Mathews, S., Michael, V., Mukherjee, P., Pargal, P., Paul, R., Phillip, A., Phillips, R., Samuel, A., Singh, N., Singh, I., Singh, A., Grewal, S. S., Singhania, A., Thirumalai, S., Varghese, A., Wesley, J., Thomas, J., Zechariah, P., Ifthikar, M. A., Mathew, R. T., Shetty, R., Vijaykumar, M. V., Hameed, B. M. Z., Ibrahim, S., Jyothish, G., Krishna, S., Mathew, S., Kumar, A. S., Sinha, P. K., Sridhar, R., Agarwal, S., Balasubramaniam, S., Chhatrapati, S., Deshpande, C., Dharia, A., Fernandes, S., Gore, M., Jayakumar, A., Mhamane, R., Nirgude, A., Parab, S., Patil, M., Peswani, A., Sahu, A., Samel, S., Shah, F., Haridas, D., Shetty, V., Abraham, B., Agarwal, V., Ahmad, Q., Asari, A., Attar, M. I., Ayyalasomayajula, N. S., Bachawat, S., Bachhav, S., Badhe, V., Badhwar, S., Basa, V. I. K. A. S., Bothara, V., Chattopadhyay, S., Chaudhari, S., Chavan, R., Chawathe, P., Dadhich, S., Dalal, A., Date, A., Deshpande, M., Dev, P., Dongre, N., Doshi, A., Gade, M., Gajjar, S., Gawande, M., Ghalme, A., Ghugare, B., Gupta, I., Jain, M., Jenasamant, S. S., Joshi, V., Kalwadia, N., Kapadia, N., Kattana, H. B. R., Kaushik, T., Kayal, A., Kovale, S., Kulkarni, Y., Kumar, K., Kumawat, K., Lad, V., Maskara, N., Mistry, R., Mohanty, S. R., Motwani, K., Mulchandani, M., Nadkarni, M., Pandey, S., Parab, M., Pardiwala, D., Patkar, A., Pawar, N., Pawar, A., Pednekar, A., Peshattiwar, V., Pokharkar, H., Potdar, O., Pothare, A., Rahmani, F., Rajput, S., Narendra, N. R., Rao, A., Rao, S., Rohela, H., Sakhrekar, R., Salunkhe, D., Sandlas, G., Sarkar, H., Satpathy, A., Sekhar, R., Shelke, Y., Shetty, S. S., Shetye, S., Kulkarni, A. S., Singal, U., Solanki, F., Sonawane, R., Thete, R., Vhatkar, R., Vora, S., Waigankar, S., Wasnik, S., Yadav, M., Yedave, R., Acharya, H., Bangar, A., Bharucha, M., Dhumane, P., Karmarkar, S., Nathani, R., Nehe, A., Nene, A., Noronha, W. J., Palapalle, N., Patel, P., Poyyil, D., Redkar, R., Shah, M., Tewari, S., Bakshi, G., Chaudhari, V., Deshmukh, A., Desoouza, A., Nair, D., Nayak, P., Patkar, S., Puri, A., Qureshi, S., Shetty, P., Shylasree, T., Thakkar, P., Thiagarajan, S., Tiwari, V. K., Voppuru, S. R., Soni, A., Soni, G., Alam, J., Bagaria, D., Bajpai, M., Bisoi, A. K., Chauhan, S., Choudhary, N., Chouhan, R. S., Chumber, S., Farooque, K., Gudala, V., Joshi, M., Kabra, A., Kale, S. S., Kumar, S., Mahajan, D., Malhotra, R., Menon, P. R., Misra, B., Mittal, S., Parshad, R., Priyadarshini, P., Sagar, S., Sharma, P. B., Sharma, V., Trikha, V., Tyagi, M., Bansal, K., Varma, K., Bhardwaj, R., Mittal, A., Ponnusamy, S., Singh, G. R., Tuli, I., Bhor, P., Dhar, S., Kale, S., Aggarwal, M., Gupta, H., Deshpande, A., Gadekar, A., Jaysingani, T., Panjwani, T., Patil, R., Vaidya, N., Vishwakarma, S. K., Wayal, U., Dutta, D., Arora, R., Dhingra, M., Garg, P. K., Huda, F., Kandwal, P., Kant, R., Seenivasagam, R. K., Joshua, L. M., Poonia, D. R., Rajput, D., Sadhasivam, S., Singh, V., Chandanwale, K., Philip, M., Thorat, V., Choudhury, Y., Das, D., Das, M., Goala, S., Laskar, F. Y., Laskar, P., Malik, K., Sarkar, A., Singha, S. T., Singha, M. N., Singha, D., Srungavarapu, G., Tapkire, R., Tling, S., Andrabi, S. M. I., Bhat, G. A., Chowdri, N., Kour, R., Parray, F., Shah, Z. A. M. I. R. A. H. M. A. D., Wani, R., Adamala, S., Gowder, R., Hegde, S., Mashitha, M. S., Sreeram, S., Ankadavar, S., Bafna, D., Dhanani, B., Ingle, N., Jadhao, P., Joseph, S., Kapote, S., Karkada, S., Lad, P., Lohia, R., Madje, S., Narasiman, V., Chisthi, M., George, G., Jothi, H., Pareed, D., Mathew, G. D. C., Abel, L., Agrawal, M., Rabindranath, B., Baldia, M., Barla, R. K., Beck, M., Benjamin, S., Bliss, J., Cherian, L., Devarakonda, S., Ete, G., George, A. J. P., and Franceschini G. (ORCID:0000-0002-2950-3395)
- Abstract
SARS-CoV-2 has been associated with an increased rate of venous thromboembolism in critically ill patients. Since surgical patients are already at higher risk of venous thromboembolism than general populations, this study aimed to determine if patients with peri-operative or prior SARS-CoV-2 were at further increased risk of venous thromboembolism. We conducted a planned sub-study and analysis from an international, multicentre, prospective cohort study of elective and emergency patients undergoing surgery during October 2020. Patients from all surgical specialties were included. The primary outcome measure was venous thromboembolism (pulmonary embolism or deep vein thrombosis) within 30 days of surgery. SARS-CoV-2 diagnosis was defined as peri-operative (7 days before to 30 days after surgery); recent (1–6 weeks before surgery); previous (≥7 weeks before surgery); or none. Information on prophylaxis regimens or pre-operative anti-coagulation for baseline comorbidities was not available. Postoperative venous thromboembolism rate was 0.5% (666/123,591) in patients without SARS-CoV-2; 2.2% (50/2317) in patients with peri-operative SARS-CoV-2; 1.6% (15/953) in patients with recent SARS-CoV-2; and 1.0% (11/1148) in patients with previous SARS-CoV-2. After adjustment for confounding factors, patients with peri-operative (adjusted odds ratio 1.5 (95%CI 1.1–2.0)) and recent SARS-CoV-2 (1.9 (95%CI 1.2–3.3)) remained at higher risk of venous thromboembolism, with a borderline finding in previous SARS-CoV-2 (1.7 (95%CI 0.9–3.0)). Overall, venous thromboembolism was independently associated with 30-day mortality (5.4 (95%CI 4.3–6.7)). In patients with SARS-CoV-2, mortality without venous thromboembolism was 7.4% (319/4342) and with venous thromboembolism was 40.8% (31/76). Patients undergoing surgery with peri-operative or recent SARS-CoV-2 appear to be at increased risk of postoperative venous thromboembolism compared with patients with no history of
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- 2022
105. Severe Neuro-COVID is associated with peripheral immune signatures, autoimmunity and neurodegeneration: a prospective cross-sectional study
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Etter, Manina M; https://orcid.org/0000-0002-2889-8305, Martins, Tomás A; https://orcid.org/0000-0001-6016-2288, Kulsvehagen, Laila; https://orcid.org/0000-0001-5236-8323, Pössnecker, Elisabeth; https://orcid.org/0000-0002-6271-2404, Duchemin, Wandrille, Hogan, Sabrina; https://orcid.org/0000-0003-3994-8109, Sanabria-Diaz, Gretel, Müller, Jannis; https://orcid.org/0000-0003-1394-8231, Chiappini, Alessio, Rychen, Jonathan, Eberhard, Noëmi, Guzman, Raphael, Mariani, Luigi, Melie-Garcia, Lester, Keller, Emanuela; https://orcid.org/0000-0002-7560-7574, Jelcic, Ilijas; https://orcid.org/0000-0003-3090-7319, Pargger, Hans; https://orcid.org/0000-0002-1234-7568, Siegemund, Martin; https://orcid.org/0000-0002-2013-4140, Kuhle, Jens, Oechtering, Johanna, Eich, Caroline, Tzankov, Alexandar; https://orcid.org/0000-0002-1100-3819, Matter, Matthias S; https://orcid.org/0000-0002-2005-5266, Uzun, Sarp, Yaldizli, Özgür, Lieb, Johanna M; https://orcid.org/0000-0002-9407-6473, Psychogios, Marios-Nikos, Leuzinger, Karoline; https://orcid.org/0000-0002-5654-9356, Hirsch, Hans H; https://orcid.org/0000-0003-0883-0423, Granziera, Cristina, Pröbstel, Anne-Katrin; https://orcid.org/0000-0002-7748-1872, Hutter, Gregor, Etter, Manina M; https://orcid.org/0000-0002-2889-8305, Martins, Tomás A; https://orcid.org/0000-0001-6016-2288, Kulsvehagen, Laila; https://orcid.org/0000-0001-5236-8323, Pössnecker, Elisabeth; https://orcid.org/0000-0002-6271-2404, Duchemin, Wandrille, Hogan, Sabrina; https://orcid.org/0000-0003-3994-8109, Sanabria-Diaz, Gretel, Müller, Jannis; https://orcid.org/0000-0003-1394-8231, Chiappini, Alessio, Rychen, Jonathan, Eberhard, Noëmi, Guzman, Raphael, Mariani, Luigi, Melie-Garcia, Lester, Keller, Emanuela; https://orcid.org/0000-0002-7560-7574, Jelcic, Ilijas; https://orcid.org/0000-0003-3090-7319, Pargger, Hans; https://orcid.org/0000-0002-1234-7568, Siegemund, Martin; https://orcid.org/0000-0002-2013-4140, Kuhle, Jens, Oechtering, Johanna, Eich, Caroline, Tzankov, Alexandar; https://orcid.org/0000-0002-1100-3819, Matter, Matthias S; https://orcid.org/0000-0002-2005-5266, Uzun, Sarp, Yaldizli, Özgür, Lieb, Johanna M; https://orcid.org/0000-0002-9407-6473, Psychogios, Marios-Nikos, Leuzinger, Karoline; https://orcid.org/0000-0002-5654-9356, Hirsch, Hans H; https://orcid.org/0000-0003-0883-0423, Granziera, Cristina, Pröbstel, Anne-Katrin; https://orcid.org/0000-0002-7748-1872, and Hutter, Gregor
- Abstract
Growing evidence links COVID-19 with acute and long-term neurological dysfunction. However, the pathophysiological mechanisms resulting in central nervous system involvement remain unclear, posing both diagnostic and therapeutic challenges. Here we show outcomes of a cross-sectional clinical study (NCT04472013) including clinical and imaging data and corresponding multidimensional characterization of immune mediators in the cerebrospinal fluid (CSF) and plasma of patients belonging to different Neuro-COVID severity classes. The most prominent signs of severe Neuro-COVID are blood-brain barrier (BBB) impairment, elevated microglia activation markers and a polyclonal B cell response targeting self-antigens and non-self-antigens. COVID-19 patients show decreased regional brain volumes associating with specific CSF parameters, however, COVID-19 patients characterized by plasma cytokine storm are presenting with a non-inflammatory CSF profile. Post-acute COVID-19 syndrome strongly associates with a distinctive set of CSF and plasma mediators. Collectively, we identify several potentially actionable targets to prevent or intervene with the neurological consequences of SARS-CoV-2 infection.
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- 2022
106. Vaccination with designed neopeptides induces intratumoral, cross-reactive CD4+ T cell responses in glioblastoma
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Wang, Jian; https://orcid.org/0000-0002-4127-322X, Weiss, Tobias; https://orcid.org/0000-0002-5533-9429, Neidert, Marian C; https://orcid.org/0000-0003-2828-4706, Toussaint, Nora C; https://orcid.org/0000-0001-7911-7647, Naghavian, Reza; https://orcid.org/0000-0002-1328-4095, Moreno Sellés, Carla; https://orcid.org/0000-0002-6982-8602, Foege, Magdalena; https://orcid.org/0000-0002-6835-6375, Tomas Ojer, Paula; https://orcid.org/0000-0003-3173-7534, Medici, Gioele; https://orcid.org/0000-0003-2279-6014, Jelcic, Ivan; https://orcid.org/0000-0002-6187-7098, Schulz, Daniel; https://orcid.org/0000-0002-0913-1678, Rushing, Elisabeth; https://orcid.org/0000-0001-7616-6320, Dettwiler, Susanne; https://orcid.org/0000-0003-1169-6296, Schrörs, Barbara; https://orcid.org/0000-0001-9758-250X, Shin, Joo Heon; https://orcid.org/0000-0002-5563-8605, McKay, Ron; https://orcid.org/0000-0001-7527-432X, Wu, Catherine J; https://orcid.org/0000-0002-3348-5054, Lutterotti, Andreas; https://orcid.org/0000-0003-1301-2863, Sospedra, Mireia; https://orcid.org/0000-0001-8333-7423, Moch, Holger; https://orcid.org/0000-0002-7986-2839, Greiner, Erich F; https://orcid.org/0000-0001-9550-1606, Bodenmiller, Bernd; https://orcid.org/0000-0002-6325-7861, Regli, Luca; https://orcid.org/0000-0003-4639-4474, Weller, Michael; https://orcid.org/0000-0002-1748-174X, Roth, Patrick; https://orcid.org/0000-0003-3897-214X, Martin, Roland; https://orcid.org/0000-0002-0982-1329, Wang, Jian; https://orcid.org/0000-0002-4127-322X, Weiss, Tobias; https://orcid.org/0000-0002-5533-9429, Neidert, Marian C; https://orcid.org/0000-0003-2828-4706, Toussaint, Nora C; https://orcid.org/0000-0001-7911-7647, Naghavian, Reza; https://orcid.org/0000-0002-1328-4095, Moreno Sellés, Carla; https://orcid.org/0000-0002-6982-8602, Foege, Magdalena; https://orcid.org/0000-0002-6835-6375, Tomas Ojer, Paula; https://orcid.org/0000-0003-3173-7534, Medici, Gioele; https://orcid.org/0000-0003-2279-6014, Jelcic, Ivan; https://orcid.org/0000-0002-6187-7098, Schulz, Daniel; https://orcid.org/0000-0002-0913-1678, Rushing, Elisabeth; https://orcid.org/0000-0001-7616-6320, Dettwiler, Susanne; https://orcid.org/0000-0003-1169-6296, Schrörs, Barbara; https://orcid.org/0000-0001-9758-250X, Shin, Joo Heon; https://orcid.org/0000-0002-5563-8605, McKay, Ron; https://orcid.org/0000-0001-7527-432X, Wu, Catherine J; https://orcid.org/0000-0002-3348-5054, Lutterotti, Andreas; https://orcid.org/0000-0003-1301-2863, Sospedra, Mireia; https://orcid.org/0000-0001-8333-7423, Moch, Holger; https://orcid.org/0000-0002-7986-2839, Greiner, Erich F; https://orcid.org/0000-0001-9550-1606, Bodenmiller, Bernd; https://orcid.org/0000-0002-6325-7861, Regli, Luca; https://orcid.org/0000-0003-4639-4474, Weller, Michael; https://orcid.org/0000-0002-1748-174X, Roth, Patrick; https://orcid.org/0000-0003-3897-214X, and Martin, Roland; https://orcid.org/0000-0002-0982-1329
- Abstract
Purpose: The low mutational load of some cancers is considered one reason for the difficulty to develop effective tumor vaccines. To overcome this problem, we developed a strategy to design neopeptides through single amino acid mutations to enhance their immunogenicity. Experimental design: Exome and RNA sequencing as well as in silico HLA-binding predictions to autologous HLA molecules were used to identify candidate neopeptides. Subsequently, in silico HLA-anchor placements were used to deduce putative T-cell receptor (TCR) contacts of peptides. Single amino acids of TCR contacting residues were then mutated by amino acid replacements. Overall, 175 peptides were synthesized and sets of 25 each containing both peptides designed to bind to HLA class I and II molecules applied in the vaccination. Upon development of a tumor recurrence, the tumor-infiltrating lymphocytes (TIL) were characterized in detail both at the bulk and clonal level. Results: The immune response of peripheral blood T cells to vaccine peptides, including natural peptides and designed neopeptides, gradually increased with repetitive vaccination, but remained low. In contrast, at the time of tumor recurrence, CD8+ TILs and CD4+ TILs responded to 45% and 100%, respectively, of the vaccine peptides. Furthermore, TIL-derived CD4+ T-cell clones showed strong responses and tumor cell lysis not only against the designed neopeptide but also against the unmutated natural peptides of the tumor. Conclusions: Turning tumor self-peptides into foreign antigens by introduction of designed mutations is a promising strategy to induce strong intratumoral CD4+ T-cell responses in a cold tumor like glioblastoma.
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- 2022
107. Dynamics of Inflammatory and Neurodegenerative Biomarkers after Autologous Hematopoietic Stem Cell Transplantation in Multiple Sclerosis
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Ruder, Josefine; https://orcid.org/0000-0002-3139-4052, Dinner, Gianna, Maceski, Aleksandra, Berenjeno-Correa, Ernesto, Müller, Antonia Maria; https://orcid.org/0000-0003-4420-9466, Jelcic, Ilijas; https://orcid.org/0000-0003-3090-7319, Kuhle, Jens, Martin, Roland; https://orcid.org/0000-0002-0982-1329, Ruder, Josefine; https://orcid.org/0000-0002-3139-4052, Dinner, Gianna, Maceski, Aleksandra, Berenjeno-Correa, Ernesto, Müller, Antonia Maria; https://orcid.org/0000-0003-4420-9466, Jelcic, Ilijas; https://orcid.org/0000-0003-3090-7319, Kuhle, Jens, and Martin, Roland; https://orcid.org/0000-0002-0982-1329
- Abstract
Autologous hematopoietic stem cell transplantation (aHSCT) is a highly efficient treatment of multiple sclerosis (MS), and hence it likely normalizes pathological and/or enhances beneficial processes in MS. The disease pathomechanisms include neuroinflammation, glial cell activation and neuronal damage. We studied biomarkers that in part reflect these, like markers for neuroinflammation (C-X-C motif chemokine ligand (CXCL) 9, CXCL10, CXCL13, and chitinase 3-like 1 (CHI3L1)), glial perturbations (glial fibrillary acidic protein (GFAP) and in part CHI3L1), and neurodegeneration (neurofilament light chain (NfL)) by enzyme-linked immunosorbent assays (ELISA) and single-molecule array assay (SIMOA) in the serum and cerebrospinal fluid (CSF) of 32 MS patients that underwent aHSCT. We sampled before and at 1, 3, 6, 12, 24 and 36 months after aHSCT for serum, as well as before and 24 months after aHSCT for CSF. We found a strong increase of serum CXCL10, NfL and GFAP one month after the transplantation, which normalized one and two years post-aHSCT. CXCL10 was particularly increased in patients that experienced reactivation of cytomegalovirus (CMV) infection, but not those with Epstein-Barr virus (EBV) reactivation. Furthermore, patients with CMV reactivation showed increased Th1 phenotype in effector memory CD4+ T cells. Changes of the other serum markers were more subtle with a trend for an increase in serum CXCL9 early post-aHSCT. In CSF, GFAP levels were increased 24 months after aHSCT, which may indicate sustained astroglia activation 24 months post-aHSCT. Other CSF markers remained largely stable. We conclude that MS-related biomarkers indicate neurotoxicity early after aHSCT that normalizes after one year while astrocyte activation appears increased beyond that, and increased serum CXCL10 likely does not reflect inflammation within the central nervous system (CNS) but rather occurs in the context of CMV reactivation or other infections post-aHSCT.
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- 2022
108. Comparison of Two Different Canine Anti-IgG Antibodies for Assessment of Oligoclonal Bands in Cerebrospinal Fluid and Serum of Dogs via Isoelectric Focusing Followed by an Immunoblot
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Prümmer, Julia K, Stein, Veronika M, Marti, Eliane; https://orcid.org/0000-0003-1284-4350, Ziegler, Mario, Lutterotti, Andreas, Jelcic, Ilijas; https://orcid.org/0000-0003-3090-7319, Steffen, Frank, Buch, Thorsten; https://orcid.org/0000-0002-2236-9074, Maiolini, Arianna, Prümmer, Julia K, Stein, Veronika M, Marti, Eliane; https://orcid.org/0000-0003-1284-4350, Ziegler, Mario, Lutterotti, Andreas, Jelcic, Ilijas; https://orcid.org/0000-0003-3090-7319, Steffen, Frank, Buch, Thorsten; https://orcid.org/0000-0002-2236-9074, and Maiolini, Arianna
- Abstract
Isoelectric focusing followed by immunoblotting is a method routinely used in human medicine to assess the presence of oligoclonal bands (OCBs) in cerebrospinal fluid (CSF) and serum. The detection of OCBs is a valuable diagnostic test, especially important in patients with the suspicion of multiple sclerosis (MS), in which at least two OCBs are found in the CSF not present in paired serum samples in up to 95% of patients. So far, presence of OCBs in CSF and serum of dogs has only been investigated in a small cohort of dogs diagnosed with degenerative myelopathy and healthy dogs. The main objective of the current study was to describe the method used for OCB detection and compare two different canine anti-IgG antibodies: a canine rabbit-anti-IgG antibody (Jackson ImmunoResearch) vs. a canine goat-anti-IgG antibody (Bio-Rad). The method was performed according to the instructions of the commercial kit used. The canine goat-anti-IgG antibody showed a better performance than the canine rabbit-anti-IgG antibody. The availability of the technique of OCB detection in the dog paves the way for further studies, especially in the field of inflammatory diseases of the canine central nervous system, and comparison between specific human and canine diseases.
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- 2022
109. Severe Neuro-COVID is associated with peripheral immune signatures, autoimmunity and signs of neurodegeneration: a prospective cross-sectional study
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Etter, Manina M; https://orcid.org/0000-0002-2889-8305, A. Martins, Tomás, Kulsvehagen, Laila; https://orcid.org/0000-0001-5236-8323, et al, Keller, Emanuela; https://orcid.org/0000-0002-7560-7574, Jelcic, Ilijas; https://orcid.org/0000-0003-3090-7319, Etter, Manina M; https://orcid.org/0000-0002-2889-8305, A. Martins, Tomás, Kulsvehagen, Laila; https://orcid.org/0000-0001-5236-8323, et al, Keller, Emanuela; https://orcid.org/0000-0002-7560-7574, and Jelcic, Ilijas; https://orcid.org/0000-0003-3090-7319
- Abstract
IMPORTANCE: Growing evidence suggests that coronavirus disease 2019 (COVID-19) is associated with neurological sequelae. However, the underlying pathophysiological mechanisms resulting in central nervous system (CNS) derogation remain unclear. OBJECTIVE: To identify severity-dependent immune mechanisms in the cerebrospinal fluid (CSF) and plasma of COVID-19 patients and their association with brain imaging alterations. DESIGN: Prospective cross-sectional cohort study. SETTING: This study was performed from August 2020 to April 2021. Participants were enrolled in the outpatient clinics, hospital wards and intensive care units (ICU) of two clinical sites in Basel and Zurich, Switzerland. PARTICIPANTS: Age >18 years and a positive SARS-CoV-2 test result were inclusion criteria. Potentially matching individuals were identified (n=310), of which 269 declined to participate and 1 did not match inclusion criteria. Paired CSF and plasma samples, as well as brain images, were acquired. The COVID-19 cohort (n=40; mean [SD] age, 54 [20] years; 17 women (42%)) was prospectively assorted by neurological symptom severity (classes I, II and III). Age/sex-matched inflammatory (n=25) and healthy (n=25) CSF and plasma control samples were obtained. For volumetric brain analysis, a healthy age/sex-matched control cohort (n=36) was established.
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- 2022
110. Radiation modified high impact polystyrene
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Jelčić, Želimir and Ranogajec, Franjo
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- 2012
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111. Whole Genome Sequencing Reveals a Chromosome 9p Deletion Causing DOCK8 Deficiency in an Adult Diagnosed with Hyper IgE Syndrome Who Developed Progressive Multifocal Leukoencephalopathy
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G. Day-Williams, Aaron, Sun, Chao, Jelcic, Ilijas, McLaughlin, Helen, Harris, Tim, Martin, Roland, and Carulli, John P.
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- 2015
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112. Identification of four novel T cell autoantigens and personal autoreactive profiles in multiple sclerosis
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Bronge, Mattias, primary, Högelin, Klara Asplund, additional, Thomas, Olivia G., additional, Ruhrmann, Sabrina, additional, Carvalho-Queiroz, Claudia, additional, Nilsson, Ola B., additional, Kaiser, Andreas, additional, Zeitelhofer, Manuel, additional, Holmgren, Erik, additional, Linnerbauer, Mathias, additional, Adzemovic, Milena Z., additional, Hellström, Cecilia, additional, Jelcic, Ivan, additional, Liu, Hao, additional, Nilsson, Peter, additional, Hillert, Jan, additional, Brundin, Lou, additional, Fink, Katharina, additional, Kockum, Ingrid, additional, Tengvall, Katarina, additional, Martin, Roland, additional, Tegel, Hanna, additional, Gräslund, Torbjörn, additional, Al Nimer, Faiez, additional, Guerreiro-Cacais, André Ortlieb, additional, Khademi, Mohsen, additional, Gafvelin, Guro, additional, Olsson, Tomas, additional, and Grönlund, Hans, additional
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- 2022
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113. Large and Small Cerebral Vessel Involvement in Severe COVID-19
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Sebastian Winklhofer, Daniel Kirschenbaum, Zsuzsanna Varga, Adrian Waeckerlin, Sabeth Aurelia Dietler, Michael Huber, Peter Steiger, Jan Willms, Andreas Lutterotti, Marcellina Isabelle Haeberlin, Ilijas Jelcic, Francesca Porta, Lukas L. Imbach, Karl Frontzek, Christoph Stippich, Christoph Globas, Irene A Abela, Emanuela Keller, Giovanna Brandi, and University of Zurich
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10028 Institute of Medical Virology ,Male ,Contrast Media ,Antibodies, Viral ,Severity of Illness Index ,Covid ,Brain Ischemia ,10234 Clinic for Infectious Diseases ,Tertiary Care Centers ,Medicine ,neuroimaging ,Electroencephalography ,cerebrovascular disorders ,Middle Aged ,Magnetic Resonance Imaging ,coronavirus disease ,COVID-19 Nucleic Acid Testing ,ComputingMethodologies_DOCUMENTANDTEXTPROCESSING ,Consciousness Disorders ,Female ,Radiology ,10023 Institute of Intensive Care Medicine ,Cardiology and Cardiovascular Medicine ,Switzerland ,medicine.medical_specialty ,2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,Critical Illness ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,610 Medicine & health ,cerebrospinal fluid ,COVID-19 Serological Testing ,10180 Clinic for Neurosurgery ,10043 Clinic for Neuroradiology ,Severity of illness ,Humans ,Aged ,Cerebral Hemorrhage ,Ischemic Stroke ,Advanced and Specialized Nursing ,SARS-CoV-2 ,business.industry ,COVID-19 ,Cerebral Arteries ,central nervous system ,10040 Clinic for Neurology ,Tomography x ray computed ,Critical illness ,Ischemic stroke ,Brief Reports ,Neurology (clinical) ,Cerebral vessel ,Tomography, X-Ray Computed ,business - Abstract
Supplemental Digital Content is available in the text., Background and Purpose: Case series indicating cerebrovascular disorders in coronavirus disease 2019 (COVID-19) have been published. Comprehensive workups, including clinical characteristics, laboratory, electroencephalography, neuroimaging, and cerebrospinal fluid findings, are needed to understand the mechanisms. Methods: We evaluated 32 consecutive critically ill patients with COVID-19 treated at a tertiary care center from March 9 to April 3, 2020, for concomitant severe central nervous system involvement. Patients identified underwent computed tomography, magnetic resonance imaging, electroencephalography, cerebrospinal fluid analysis, and autopsy in case of death. Results: Of 32 critically ill patients with COVID-19, 8 (25%) had severe central nervous system involvement. Two presented with lacunar ischemic stroke in the early phase and 6 with prolonged impaired consciousness after termination of analgosedation. In all but one with delayed wake-up, neuroimaging or autopsy showed multiple cerebral microbleeds, in 3 with additional subarachnoid hemorrhage and in 2 with additional small ischemic lesions. In 3 patients, intracranial vessel wall sequence magnetic resonance imaging was performed for the first time to our knowledge. All showed contrast enhancement of vessel walls in large cerebral arteries, suggesting vascular wall pathologies with an inflammatory component. Reverse transcription-polymerase chain reactions for SARS-CoV-2 in cerebrospinal fluid were all negative. No intrathecal SARS-CoV-2-specific IgG synthesis was detectable. Conclusions: Different mechanisms of cerebrovascular disorders might be involved in COVID-19. Acute ischemic stroke might occur early. In a later phase, microinfarctions and vessel wall contrast enhancement occur, indicating small and large cerebral vessels involvement. Central nervous system disorders associated with COVID-19 may lead to long-term disabilities. Mechanisms should be urgently investigated to develop neuroprotective strategies.
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- 2020
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114. Severe Neuro-COVID is associated with peripheral immune signatures, autoimmunity and signs of neurodegeneration: a prospective cross-sectional study
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Manina M. Etter, Tomás A. Martins, Laila Kulsvehagen, Elisabeth Pössnecker, Wandrille Duchemin, Sabrina Hogan, Gretel Sanabria-Diaz, Jannis Müller, Alessio Chiappini, Jonathan Rychen, Noëmi Eberhard, Lester Melie-Garcia, Emanuela Keller, Ilijas Jelcic, Hans Pargger, Martin Siegemund, Jens Kuhle, Johanna Oechtering, Caroline Eich, Alexandar Tzankov, Matthias S. Matter, Özgür Yaldizli, Johanna M. Lieb, Marios-Nikos Psychogios, Caroline M. Berkemeier, Karoline Leuzinger, Hans H. Hirsch, Cristina Granziera, Anne-Katrin Pröbstel, and Gregor Hutter
- Abstract
ImportanceGrowing evidence suggests that coronavirus disease 2019 (COVID-19) is associated with neurological sequelae. However, the underlying pathophysiological mechanisms resulting in central nervous system (CNS) derogation remain unclear.ObjectiveTo identify severity-dependent immune mechanisms in the cerebrospinal fluid (CSF) and plasma of COVID-19 patients and their association with brain imaging alterations.DesignProspective cross-sectional cohort study.SettingThis study was performed from August 2020 to April 2021. Participants were enrolled in the outpatient clinics, hospital wards and intensive care units (ICU) of two clinical sites in Basel and Zurich, Switzerland.ParticipantsAge >18 years and a positive SARS-CoV-2 test result were inclusion criteria. Potentially matching individuals were identified (n=310), of which 269 declined to participate and 1 did not match inclusion criteria. Paired CSF and plasma samples, as well as brain images, were acquired. The COVID-19 cohort (n=40; mean [SD] age, 54 [20] years; 17 women (42%)) was prospectively assorted by neurological symptom severity (classes I, II and III). Age/sex-matched inflammatory (n=25) and healthy (n=25) CSF and plasma control samples were obtained. For volumetric brain analysis, a healthy age/sex-matched control cohort (n=36) was established.ExposuresLumbar puncture, blood sampling and cranial MRI and/or CT.Main outcomes and measuresProteomics, standard parameters and antibody profiling of paired CSF and plasma samples in COVID-19 patients and controls. Brain imaging and gray matter volumetric analysis in association with biomarker profiles. Follow-up after 10-months.ResultsCOVID-19 patients displayed a plasma cytokine storm but a non-inflammatory CSF profile. Class III patients displayed signs of blood-brain barrier (BBB) impairment and a polyclonal B cell response targeting self- and non-self antigens. Decreased regional brain volumes were present in COVID-19 patients and associated with specific CSF and plasma parameters.Conclusion and relevanceNeuro-COVID class III patients had a strong, peripheral immune response resulting in (1) BBB impairment (2) ingress of (auto-)antibodies, (3) microglia activation and neuronal damage signatures. Our data point towards several potentially actionable targets that may be addressed to prevent COVID-19-related neurological sequelae.Trial registrationThe trial (NCT04472013) was registered on clinicaltrials.gov.Key pointsQuestionDoes a severity-dependent pattern of immune mechanisms exist in the cerebrospinal fluid (CSF) and plasma of COVID-19 patients and are these associated with clinical and brain imaging findings?FindingsNeuro-COVID patients display a robust class III-specific peripheral immune response resulting in (1) blood-brain barrier (BBB) impairment, (2) ingress of (auto-)antibodies, (3) microglia activation and neuronal damage signatures. Integration of MRIs, brain volumetry and proteomics identified biomarkers associated with regional brain volume loss in severe Neuro-COVID.MeaningWe provide a multidimensional framework of mechanisms associated with severe Neuro-COVID and present possible targets to prevent COVID-19-related neurological sequelae.
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- 2022
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115. Oligoklonale Banden bei Hunden mit idiopathischer Epilepsie
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J Föhr, J K Prümmer, A Maiolini, E Marti, I Jelcic, A Tipold, H Volk, and V M Stein
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- 2022
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116. Characterization of Antigen-Induced CD4+ T-Cell Senescence in Multiple Sclerosis
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Paula, Tomas-Ojer, Puthenparampil, Marco, Thorsten, Hornemann, Andreas, Lutterotti, Ilijas, Jelcic, Mario, Ziegler, Andreas, J Hülsmeier, Carolina, Cruciani, Wolfgang, Faigle, Roland, Martin, and Mireia, Sospedra.
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- 2022
117. Cementitious Composites Reinforced withWaste Fibres from the Production of High-Quality Construction Textiles
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Marina Frančić Smrkić, Marija Jelcic Rukavina, Katarina Didulica, and Ana Baricevic
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waste fibres ,alkali resistant glass ,basalt ,carbon ,mortar ,General Materials Science - Abstract
In general, 20–25% of the original fibre weight is considered waste in the production of high-quality textiles for the construction sector. A market analysis has shown that in the Republic of Croatia alone, up to 327 tonnes of this waste is produced annually, which is enough to reinforce 50 to 150 thousand m3 of cementitious composites. This preliminary study aims to evaluate the contribution of glass, basalt and carbon fibres generated as waste in the local production of high-performance technical textiles, to the fresh and hardened properties of fibre reinforced mortars. In order to investigate the influence of fibres, three types of fibres in two different lengths (5 and 10 mm) were used, while the amount of fibres was constant. The obtained results show that due to the fibre presence, workability is reduced regardless of the type and length of the fibre. The tested fibres have a negligible effect on compressive strength, but the use of basalt and carbon fibres increases the tensile strength. Furthermore, all three types have positive influence on the toughness and volumetric deformations, although to a greater extent in the use of 10 mm long fibres and carbon fibres.
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- 2022
118. Dynamics of Inflammatory and Neurodegenerative Biomarkers after Autologous Hematopoietic Stem Cell Transplantation in Multiple Sclerosis
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Ruder, Josefine, Dinner, Gianna, Maceski, Aleksandra, Berenjeno-Correa, Ernesto, Müller, Antonia Maria, Jelcic, Ilijas, Kuhle, Jens, Martin, Roland, University of Zurich, and Martin, Roland
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1503 Catalysis ,1604 Inorganic Chemistry ,Organic Chemistry ,1607 Spectroscopy ,610 Medicine & health ,General Medicine ,Catalysis ,10040 Clinic for Neurology ,Computer Science Applications ,Inorganic Chemistry ,1312 Molecular Biology ,1706 Computer Science Applications ,Physical and Theoretical Chemistry ,1606 Physical and Theoretical Chemistry ,Molecular Biology ,Spectroscopy ,1605 Organic Chemistry - Published
- 2022
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119. Severe Neuro-COVID is associated with peripheral immune signatures, autoimmunity and signs of neurodegeneration: a prospective cross-sectional study
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Etter, Manina M, A. Martins, Tomás, Kulsvehagen, Laila, et al, Keller, Emanuela, Jelcic, Ilijas, and University of Zurich
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10180 Clinic for Neurosurgery ,610 Medicine & health - Published
- 2022
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120. Impaired Inhibitory Fcγ Receptor IIB Expression on B Cells in Chronic Inflammatory Demyelinating Polyneuropathy
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Tackenberg, Björn, Jelčić, Ilijas, Baerenwaldt, Anne, Oertel, Wolfgang H., Sommer, Norbert, Nimmerjahn, Falk, Lünemann, Jan D., and Ravetch, Jeffrey
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- 2009
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121. T-Cell Specificity Influences Disease Heterogeneity in Multiple Sclerosis
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Paula Tomas-Ojer, Mireia Sospedra, Roland Martin, Raquel Planas, Ivan Jelcic, Carla A. Wicki, Praveena Manogaran, Roland Opfer, Marco Puthenparampil, Ilijas Jelcic, Maria Jose Docampo, Carolina Cruciani, Markus Reindl, Andreas Lutterotti, and University of Zurich
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Adult ,Male ,Multiple Sclerosis ,T-Lymphocytes ,Clinical Neurology ,610 Medicine & health ,T-Cell Antigen Receptor Specificity ,Article ,Myelin oligodendrocyte glycoprotein ,Transcriptome ,Myelin ,Immunophenotyping ,Antigen ,medicine ,Humans ,Interferon gamma ,Autoimmune disease ,biology ,business.industry ,Multiple sclerosis ,Middle Aged ,medicine.disease ,Magnetic Resonance Imaging ,10040 Clinic for Neurology ,2728 Neurology (clinical) ,medicine.anatomical_structure ,Neurology ,2808 Neurology ,Immunology ,biology.protein ,Female ,Myelin-Oligodendrocyte Glycoprotein ,Neurology (clinical) ,business ,medicine.drug - Abstract
Background and Objectives Encouraged by the enormous progress that the identification of specific autoantigens added to the understanding of neurologic autoimmune diseases, we undertook here an in-depth study of T-cell specificities in the autoimmune disease multiple sclerosis (MS), for which the spectrum of responsible autoantigens is not fully defined yet. The identification of target antigens in MS is crucial for therapeutic strategies aimed to induce antigen-specific tolerance. In addition, knowledge of relevant T-cell targets can improve our understanding of disease heterogeneity, a hallmark of MS that complicates clinical management. Methods The proliferative response and interferon gamma (IFN-γ) release of CSF-infiltrating CD4+ T cells from patients with MS against several autoantigens was used to identify patients with different intrathecal T-cell specificities. Fresh CSF-infiltrating and paired circulating lymphocytes in these patients were characterized in depth by ex vivo immunophenotyping and transcriptome analysis of relevant T-cell subsets. Further examination of these patients included CSF markers of inflammation and neurodegeneration and a detailed characterization with respect to demographic, clinical, and MRI features. Results By testing CSF-infiltrating CD4+ T cells from 105 patients with MS against seven long-known myelin and five recently described GDP-l-fucose synthase peptides, we identified GDP-l-fucose synthase and myelin oligodendrocyte glycoprotein (35-55) responder patients. Immunophenotyping of CSF and paired blood samples in these patients revealed a significant expansion of an effector memory (CCR7− CD45RA−) CD27− Th1 CD4+ cell subset in GDP-l-fucose synthase responders. Subsequent transcriptome analysis of this subset demonstrated expression of Th1 and cytotoxicity-associated genes. Patients with different intrathecal T-cell specificities also differ regarding inflammation- and neurodegeneration-associated biomarkers, imaging findings, expression of HLA class II alleles, and seasonal distribution of the time of the lumbar puncture. Discussion Our observations reveal an association between autoantigen reactivity and features of disease heterogeneity that strongly supports an important role of T-cell specificity in MS pathogenesis. These data have the potential to improve patient classification in clinical practice and to guide the development of antigen-specific tolerization strategies., Neurology: Neuroimmunology & Neuroinflammation, 8 (6), ISSN:2332-7812
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- 2021
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122. Severe Neuro-COVID is associated with peripheral immune signatures, autoimmunity and neurodegeneration: a prospective cross-sectional study
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Etter, Manina, primary, Martins, Tomás, additional, Kulsvehagen, Laila, additional, Pössnecker, Elisabeth, additional, Duchemin, Wandrille, additional, Hogan, Sabrina, additional, Sanabria-Diaz, Gretel, additional, Müller, Jannis, additional, Chiappini, Alessio, additional, Rychen, Jonathan, additional, Eberhard, Noëmi, additional, Guzman, Raphael, additional, MarianI, Luigi, additional, Keller, Emanuela, additional, Melie-Garcia, Lester, additional, Jelcic, Ilijas, additional, Pargger, Hans, additional, Siegemund, Martin, additional, Kuhle, Jens, additional, Oechtering, Johanna, additional, Eich, Caroline, additional, Tzankov, Alexandar, additional, Matter, Matthias, additional, Yaldizli, Özgür, additional, Lieb, Johanna, additional, Psychogios, Marios, additional, Berkemeier, Caroline, additional, Leuzinger, Karoline, additional, Hirsch, Hans, additional, Granziera, Cristina, additional, Pröbstel, Anne-Katrin, additional, and Hutter, Gregor, additional
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- 2022
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123. Severe Neuro-COVID is associated with peripheral immune signatures, autoimmunity and signs of neurodegeneration: a prospective cross-sectional study
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Etter, Manina M., primary, A. Martins, Tomás, additional, Kulsvehagen, Laila, additional, Pössnecker, Elisabeth, additional, Duchemin, Wandrille, additional, Hogan, Sabrina, additional, Sanabria-Diaz, Gretel, additional, Müller, Jannis, additional, Chiappini, Alessio, additional, Rychen, Jonathan, additional, Eberhard, Noëmi, additional, Melie-Garcia, Lester, additional, Keller, Emanuela, additional, Jelcic, Ilijas, additional, Pargger, Hans, additional, Siegemund, Martin, additional, Kuhle, Jens, additional, Oechtering, Johanna, additional, Eich, Caroline, additional, Tzankov, Alexandar, additional, Matter, Matthias S., additional, Yaldizli, Özgür, additional, Lieb, Johanna M., additional, Psychogios, Marios-Nikos, additional, Berkemeier, Caroline M., additional, Leuzinger, Karoline, additional, Hirsch, Hans H., additional, Granziera, Cristina, additional, Pröbstel, Anne-Katrin, additional, and Hutter, Gregor, additional
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- 2022
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124. Oligoklonale Banden bei Hunden mit idiopathischer Epilepsie
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Föhr, J, additional, Prümmer, J K, additional, Maiolini, A, additional, Marti, E, additional, Jelcic, I, additional, Tipold, A, additional, Volk, H, additional, and Stein, V M, additional
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- 2022
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125. Enhanced Anaerobic Biodegradability and Inactivation of Fecal Coliforms and Salmonella spp. in Wastewater Sludge by Using Microwaves
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Pino-Jelcic, Sergio A., Hong, Seung Mo, and Park, Jae K.
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- 2006
126. A synergy between mechanosensitive calcium- and membrane-binding mediates tension-sensing by C2-like domains
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Zhouyang Shen, Kalina T. Belcheva, Mark Jelcic, King Lam Hui, Anushka Katikaneni, and Philipp Niethammer
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cPLA2 ,Multidisciplinary ,calcium ,Nuclear Envelope ,Group IV Phospholipases A2 ,nucleus ,Lipid Bilayers ,Cell Biology ,Biological Sciences ,Mechanotransduction, Cellular ,Protein Domains ,Humans ,Surface Tension ,membrane ,mechanotransduction - Abstract
Significance A cell must be able to measure whether the lipid membranes that surround its insides are stretched. Currently, mechanosensitive ion channels are the best-studied class of membrane tension sensors, but recent work suggests that peripheral membrane enzymes that gauge nuclear confinement or swelling during cell migration or upon tissue injury constitute a second class. The mechanosensitivity of these enzymes derives from their calcium-dependent (“C2-like”) membrane-interaction domains. Although these can be found in many important signaling proteins, they have remained virtually unstudied as mechanotransducers. How membrane tension controls these domains and what features render them mechanosensitive is unclear. Here, we show that membrane tension-sensing by C2-like domains is mediated by a synergy between mechanosensitive calcium-binding and membrane insertion., When nuclear membranes are stretched, the peripheral membrane enzyme cytosolic phospholipase A2 (cPLA2) binds via its calcium-dependent C2 domain (cPLA2-C2) and initiates bioactive lipid signaling and tissue inflammation. More than 150 C2-like domains are encoded in vertebrate genomes. How many of them are mechanosensors and quantitative relationships between tension and membrane recruitment remain unexplored, leaving a knowledge gap in the mechanotransduction field. In this study, we imaged the mechanosensitive adsorption of cPLA2 and its C2 domain to nuclear membranes and artificial lipid bilayers, comparing it to related C2-like motifs. Stretch increased the Ca2+ sensitivity of all tested domains, promoting half-maximal binding of cPLA2 at cytoplasmic resting-Ca2+ concentrations. cPLA2-C2 bound up to 50 times tighter to stretched than to unstretched membranes. Our data suggest that a synergy of mechanosensitive Ca2+ interactions and deep, hydrophobic membrane insertion enables cPLA2-C2 to detect stretched membranes with antibody-like affinity, providing a quantitative basis for understanding mechanotransduction by C2-like domains.
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- 2021
127. Contemporary issues with stuttering: The Fourth Croatia Stuttering Symposium
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Lowe, Robyn, Jelčić Jakšić, Suzana, Onslow, Mark, O’Brian, Sue, Vanryckeghem, Martine, Millard, Sharon, Kelman, Elaine, Block, Susan, Franken, Marie-Christine, Van Eerdenbrugh, Sabine, Menzies, Ross, Shenker, Rosalee, Byrd, Courtney, Bosshardt, Hans-Georg, del Gado, Francesca, and Lim, Valerie
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- 2021
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128. When a T cell engages a B cell: novel insights in multiple sclerosis
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Mireia Sospedra, Roland Martin, Ivan Jelcic, University of Zurich, Jelcic, Ivan, and Martin, Roland
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Central Nervous System ,0301 basic medicine ,Multiple Sclerosis ,T-Lymphocytes ,T cell ,Cell ,Central nervous system ,610 Medicine & health ,2700 General Medicine ,Autoimmune Diseases ,03 medical and health sciences ,0302 clinical medicine ,B-Cell Depletion Therapy ,medicine ,Humans ,B cell ,Autoimmune disease ,B-Lymphocytes ,Effector ,business.industry ,Multiple sclerosis ,General Medicine ,medicine.disease ,10040 Clinic for Neurology ,030104 developmental biology ,medicine.anatomical_structure ,030220 oncology & carcinogenesis ,Immunology ,business - Abstract
Multiple sclerosis is an autoimmune disease of the central nervous system (CNS) in which autoreactive T cells are considered to be the major effector cells in orchestrating and promoting CNS injuries. However, B cells emerged as additional important cellular player in multiple sclerosis immunopathogenesis since B cell depletion therapy has been found to be very effective in reducing new relapses. This short review summarises important new insights into the interaction between these two cell populations and outlines recent observations regarding how memory B cells activate brain-homing autoreactive T cells in multiple sclerosis.
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- 2020
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129. Neuro-psychiatric manifestations in patients with systemic lupus erythematosus: A systematic review and results from the Swiss lupus cohort study
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Meier, Aline L, Bodmer, Nicolas S, Wirth, Carla, Bachmann, Lucas M, Ribi, Camillo, Pröbstel, Anne-Katrin, Waeber, David, Jelcic, Ilijas, Steiner, Urs C, Swiss SLE Cohort Study (SSCS), University of Zurich, and Steiner, Urs C
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2745 Rheumatology ,10033 Clinic for Immunology ,610 Medicine & health ,10040 Clinic for Neurology - Published
- 2021
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130. Autologous hematopoietic stem cell transplantation in multiple sclerosis: a global approval and availability review
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Roland Martin, Urs Schanz, Antonia M.S. Müller, K. Léger, Ilijas Jelcic, M. Foege, P. Stathopoulos, Andreas Lutterotti, University of Zurich, Stathopoulos, P, and Martin, R
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Transplantation ,business.industry ,2747 Transplantation ,medicine.medical_treatment ,Multiple sclerosis ,2720 Hematology ,MEDLINE ,610 Medicine & health ,Hematopoietic stem cell transplantation ,Hematology ,Bioinformatics ,medicine.disease ,10040 Clinic for Neurology ,Text mining ,medicine ,business - Published
- 2021
131. A synergy between mechanosensitive calcium- and membrane-binding mediates tension-sensing by C2-like domains
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Shen, Zhouyang, primary, Belcheva, Kalina T., additional, Jelcic, Mark, additional, Hui, King Lam, additional, Katikaneni, Anushka, additional, and Niethammer, Philipp, additional
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- 2021
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132. NK Cells and Innate-Like T Cells After Autologous Hematopoietic Stem Cell Transplantation in Multiple Sclerosis
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Ruder, Josefine, primary, Rex, Jordan, additional, Obahor, Simon, additional, Docampo, María José, additional, Müller, Antonia M. S., additional, Schanz, Urs, additional, Jelcic, Ilijas, additional, and Martin, Roland, additional
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- 2021
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133. Unfavorable Structural and Functional Outcomes in Myelin Oligodendrocyte Glycoprotein Antibody–Associated Optic Neuritis
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Andreas Lutterotti, Sebastian Lukas, Misha Pless, Markus Reindl, Sven Schippling, Ilijas Jelcic, Klara Landau, Konrad P Weber, Michael Weller, Roland Martin, James V M Hanson, University of Zurich, and Schippling, Sven
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10018 Ophthalmology Clinic ,Male ,Pathology ,medicine.medical_specialty ,Optic Neuritis ,Visual acuity ,Adolescent ,Visual Acuity ,Nerve fiber layer ,610 Medicine & health ,Myelin oligodendrocyte glycoprotein ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Cerebrospinal fluid ,Recurrence ,medicine ,Humans ,Optic neuritis ,Aged ,Autoantibodies ,Aquaporin 4 ,Neuromyelitis optica ,biology ,business.industry ,Optic Nerve ,Retinal ,Middle Aged ,2731 Ophthalmology ,Prognosis ,medicine.disease ,eye diseases ,10040 Clinic for Neurology ,Ophthalmology ,2728 Neurology (clinical) ,medicine.anatomical_structure ,chemistry ,030221 ophthalmology & optometry ,Optic nerve ,biology.protein ,Myelin-Oligodendrocyte Glycoprotein ,sense organs ,Neurology (clinical) ,medicine.symptom ,business ,Tomography, Optical Coherence ,030217 neurology & neurosurgery - Abstract
Background Recurrent optic neuritis (rON) associated with myelin oligodendrocyte glycoprotein (MOG)-specific antibodies has been initially reported to show a better clinical outcome than aquaporin-4 (AQP4)-seropositive ON in neuromyelitis optica spectrum disorder (NMOSD). Here, we characterize clinical and neuroimaging findings in severe cases of MOG antibody-positive and AQP4 antibody-negative bilateral rON. Methods Three male adults with rON (ages 18, 44, and 63 years) were evaluated with optical coherence tomography (OCT), MRI, cerebrospinal fluid (CSF), and serological studies. Results All patients experienced >7 relapses of ON with severe reduction of visual acuity and partial response to steroid treatment. Optic nerves were affected bilaterally, although unilateral relapses were more frequent than simultaneous bilateral recurrences. Patients were MOG-seropositive but repeatedly tested negative for AQP4 antibodies. OCT showed severe thinning of the peripapillary retinal nerve fiber layer. On MRI, contrast-enhancing lesions extended over more than half the length of the optic nerve. CSF analyses during ON episodes were normal. Severe visual deficits accumulated over time in 2 of 3 patients, despite immunosuppressive therapy. Conclusions MOG-seropositive and AQP4-seronegative rON may be associated with an aggressive disease course and poor functional and structural outcomes. In contrast to previous reports, the severity and pattern of retinal and optic nerve damage closely resembled phenotypes commonly observed in AQP4-seropositive rON without fulfilling current diagnostic criteria for NMOSD.
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- 2019
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134. Corrigendum to “The Satisfaction with Communication in Everyday Speaking Situations (SCESS) scale: An overarching outcome measure of treatment effect” [J. Fluency Disord. (2018), 58, 77–85]
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Karimi, Hamid, Onslow, Mark, Jones, Mark, O’Brian, Sue, Packman, Ann, Menzies, Ross, Reilly, Sheena, Sommer, Martin, and Jelčić-Jakšić, Suzana
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- 2021
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135. FSME: Klinik und Therapie.
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Vlad, Benjamin and Jelcic, Ilijas
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- 2022
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136. Acute Disseminated Encephalomyelitis in FET PET/MR
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Lohaus, Niklas, primary, Mader, Cäcilia, additional, Jelcic, Ilijas, additional, Reimann, Regina, additional, and Huellner, Martin W., additional
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- 2021
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137. Anti-IgLON5 Disease: A New Bulbar-Onset Motor Neuron Mimic Syndrome
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Ilijas Jelcic, Elisabeth Probst-Müller, Esther I. Schwarz, Konrad E. Bloch, Bernhard Schwizer, Andreas Lutterotti, Bettina Schreiner, Jana Werner, Hans-Heinrich Jung, Jakob Nilsson, and University of Zurich
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Pediatrics ,medicine.medical_specialty ,business.industry ,medicine.medical_treatment ,610 Medicine & health ,Immunotherapy ,Disease ,Motor neuron ,medicine.disease ,10040 Clinic for Neurology ,medicine.anatomical_structure ,2728 Neurology (clinical) ,Neurology ,Swallowing ,2808 Neurology ,medicine ,10033 Clinic for Immunology ,Bulbar onset ,Neurology (clinical) ,Respiratory system ,Amyotrophic lateral sclerosis ,Differential diagnosis ,10178 Clinic for Pneumology ,business - Abstract
ObjectiveTo expand the spectrum of anti-IgLON5 disease by adding 5 novel anti-IgLON5–seropositive cases with bulbar motor neuron disease-like phenotype.MethodsWe characterized the clinical course, brain MRI and laboratory findings, and therapy response in these 5 patients.ResultsPatients were severely affected by bulbar impairment and its respiratory consequences. Sleep-related breathing disorders and parasomnias were common. All patients showed clinical or electrophysiologic signs of motor neuron disease without fulfilling the diagnostic criteria for amyotrophic lateral sclerosis. One patient regained autonomy in swallowing and eating, possibly related to immunotherapy.ConclusionIgLON5 disease is an important differential diagnosis to evaluate in patients with bulbar motor neuron disease-like phenotype and sleep disorders. There is need for a deeper understanding of the underlying pathobiology to determine whether IgLON5 disease is an immunotherapy-responsive condition.
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- 2021
138. Altered CSF Albumin Quotient Links Peripheral Inflammation and Brain Damage in MS
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Marco Puthenparampil, Mireia Sospedra, Ilijas Jelcic, Andreas Lutterotti, Carolina Cruciani, Wolfgang Faigle, Andreas J. Hülsmeier, Mario Ziegler, Thorsten Hornemann, Paula Tomas-Ojer, Roland Martin, and University of Zurich
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Adult ,Male ,0301 basic medicine ,Pathology ,medicine.medical_specialty ,Multiple Sclerosis ,Inflammation ,610 Medicine & health ,Brain damage ,Systemic inflammation ,Article ,CHI3L1 ,Proinflammatory cytokine ,03 medical and health sciences ,0302 clinical medicine ,Immunophenotyping ,Albumins ,540 Chemistry ,Humans ,Medicine ,CSF albumin ,10038 Institute of Clinical Chemistry ,business.industry ,Albumin ,Middle Aged ,10040 Clinic for Neurology ,030104 developmental biology ,2728 Neurology (clinical) ,Neurology ,Blood-Brain Barrier ,Brain Injuries ,Immunoglobulin G ,2808 Neurology ,Female ,Neurology (clinical) ,medicine.symptom ,business ,Biomarkers ,030217 neurology & neurosurgery - Abstract
ObjectiveCNS damage can increase the susceptibility of the blood-brain barrier (BBB) to changes induced by systemic inflammation. The aim of this study is to better understand BBB permeability in patients with MS and to examine whether compromised BBB integrity in some of these patients is associated with CNS damage and systemic inflammation.MethodsRoutine CSF measurements of 121 patients with MS were analyzed including number and type of infiltrating cells, total protein, lactate, and oligoclonal bands, as well as intrathecal production of immunoglobulins and CSF/serum quotients for albumin, immunoglobulins, and glucose. In addition, in a subcohort of these patients, we performed ex vivo immunophenotyping of CSF-infiltrating and paired circulating lymphocytes using a panel of 13 monoclonal antibodies, we quantified intrathecal neurofilament light chain (NF-L) and chitinase 3-like 1 (CHI3L1), and we performed intrathecal lipidomic analysis.ResultsPatients with MS with abnormal high levels of albumin in the CSF showed a distinct CSF cell infiltrate and markers of CNS damage such as increased intrathecal levels of NF-L and CHI3L1 as well as a distinct CSF lipidomic profile. In addition, these patients showed higher numbers of circulating proinflammatory Th1 and Th1* cells compatible with systemic inflammation. Of interest, the abnormally high levels of albumin in the CSF of those patients were preserved over time.ConclusionsOur results support the hypothesis that CNS damage may increase BBB vulnerability to systemic inflammation in a subset of patients and thus contribute to disease heterogeneity.
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- 2021
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139. Anti-IgLON5 Disease
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Werner, Jana, Jelcic, Ilijas, Schwarz, Esther Irene, Probst-Müller, Elisabeth, Nilsson, Jakob, Schwizer, Bernhard, Bloch, Konrad Ernst, Lutterotti, Andreas, Jung, Hans-Heinrich, and Schreiner, Bettina
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Diagnosis, Differential ,Male ,Cell Adhesion Molecules, Neuronal ,Humans ,Female ,Immunotherapy ,Syndrome ,Middle Aged ,Motor Neuron Disease ,Article ,Aged ,Autoantibodies ,Follow-Up Studies - Abstract
Objective To expand the spectrum of anti-IgLON5 disease by adding 5 novel anti-IgLON5–seropositive cases with bulbar motor neuron disease-like phenotype. Methods We characterized the clinical course, brain MRI and laboratory findings, and therapy response in these 5 patients. Results Patients were severely affected by bulbar impairment and its respiratory consequences. Sleep-related breathing disorders and parasomnias were common. All patients showed clinical or electrophysiologic signs of motor neuron disease without fulfilling the diagnostic criteria for amyotrophic lateral sclerosis. One patient regained autonomy in swallowing and eating, possibly related to immunotherapy. Conclusion IgLON5 disease is an important differential diagnosis to evaluate in patients with bulbar motor neuron disease-like phenotype and sleep disorders. There is need for a deeper understanding of the underlying pathobiology to determine whether IgLON5 disease is an immunotherapy-responsive condition.
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- 2021
140. T cell reactivity screening reveals four novel CNS autoantigens in multiple sclerosis
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Bronge, M., Asplund Hogelin, K., Thomas, O. G., Ruhrmann, S., Carvalho-Querioz, C., Nilsson, O., Kaiser, A., Holmgren, E., Linnerbauer, M., Adzemovic, M. Z., Zeitelhofer, M., Hellström, Cecilia, Jelcic, I., Liu, Hailong, Nilsson, Peter, Hillert, J., Brundin, L., Fink, K., Martin, R., Tegel, Hanna, Gräslund, Torbjörn, Al Nimer, F., Guerreiro-Cacais, A. O., Khademi, M., Gafvelin, G., Olsson, T., Gronlund, H., Bronge, M., Asplund Hogelin, K., Thomas, O. G., Ruhrmann, S., Carvalho-Querioz, C., Nilsson, O., Kaiser, A., Holmgren, E., Linnerbauer, M., Adzemovic, M. Z., Zeitelhofer, M., Hellström, Cecilia, Jelcic, I., Liu, Hailong, Nilsson, Peter, Hillert, J., Brundin, L., Fink, K., Martin, R., Tegel, Hanna, Gräslund, Torbjörn, Al Nimer, F., Guerreiro-Cacais, A. O., Khademi, M., Gafvelin, G., Olsson, T., and Gronlund, H.
- Abstract
QC 20211206
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- 2021
141. Anti-IgLON5 Disease: A New Bulbar-Onset Motor Neuron Mimic Syndrome
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Werner, Jana, Jelcic, Ilijas, Schwarz, Esther Irene, Probst-Müller, Elisabeth, Nilsson, Jakob, Schwizer, Bernhard, Bloch, Konrad Ernst, Lutterotti, Andreas, Jung, Hans-Heinrich, Schreiner, Bettina, Werner, Jana, Jelcic, Ilijas, Schwarz, Esther Irene, Probst-Müller, Elisabeth, Nilsson, Jakob, Schwizer, Bernhard, Bloch, Konrad Ernst, Lutterotti, Andreas, Jung, Hans-Heinrich, and Schreiner, Bettina
- Abstract
OBJECTIVE: To expand the spectrum of anti-IgLON5 disease by adding 5 novel anti-IgLON5-seropositive cases with bulbar motor neuron disease-like phenotype. METHODS: We characterized the clinical course, brain MRI and laboratory findings, and therapy response in these 5 patients. RESULTS: Patients were severely affected by bulbar impairment and its respiratory consequences. Sleep-related breathing disorders and parasomnias were common. All patients showed clinical or electrophysiologic signs of motor neuron disease without fulfilling the diagnostic criteria for amyotrophic lateral sclerosis. One patient regained autonomy in swallowing and eating, possibly related to immunotherapy. CONCLUSION: IgLON5 disease is an important differential diagnosis to evaluate in patients with bulbar motor neuron disease-like phenotype and sleep disorders. There is need for a deeper understanding of the underlying pathobiology to determine whether IgLON5 disease is an immunotherapy-responsive condition.
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- 2021
142. Altered CSF Albumin Quotient Links Peripheral Inflammation and Brain Damage in MS
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Puthenparampil, Marco, Tomas-Ojer, Paula, Hornemann, Thorsten, Lutterotti, Andreas, Jelcic, Ilijas, Ziegler, Mario, Hülsmeier, Andreas J, Cruciani, Carolina, Faigle, Wolfgang, Martin, Roland, Sospedra, Mireia, Puthenparampil, Marco, Tomas-Ojer, Paula, Hornemann, Thorsten, Lutterotti, Andreas, Jelcic, Ilijas, Ziegler, Mario, Hülsmeier, Andreas J, Cruciani, Carolina, Faigle, Wolfgang, Martin, Roland, and Sospedra, Mireia
- Abstract
OBJECTIVE CNS damage can increase the susceptibility of the blood-brain barrier (BBB) to changes induced by systemic inflammation. The aim of this study is to better understand BBB permeability in patients with MS and to examine whether compromised BBB integrity in some of these patients is associated with CNS damage and systemic inflammation. METHODS Routine CSF measurements of 121 patients with MS were analyzed including number and type of infiltrating cells, total protein, lactate, and oligoclonal bands, as well as intrathecal production of immunoglobulins and CSF/serum quotients for albumin, immunoglobulins, and glucose. In addition, in a subcohort of these patients, we performed ex vivo immunophenotyping of CSF-infiltrating and paired circulating lymphocytes using a panel of 13 monoclonal antibodies, we quantified intrathecal neurofilament light chain (NF-L) and chitinase 3-like 1 (CHI3L1), and we performed intrathecal lipidomic analysis. RESULTS Patients with MS with abnormal high levels of albumin in the CSF showed a distinct CSF cell infiltrate and markers of CNS damage such as increased intrathecal levels of NF-L and CHI3L1 as well as a distinct CSF lipidomic profile. In addition, these patients showed higher numbers of circulating proinflammatory Th1 and Th1* cells compatible with systemic inflammation. Of interest, the abnormally high levels of albumin in the CSF of those patients were preserved over time. CONCLUSIONS Our results support the hypothesis that CNS damage may increase BBB vulnerability to systemic inflammation in a subset of patients and thus contribute to disease heterogeneity.
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- 2021
143. NK Cells and Innate-Like T Cells After Autologous Hematopoietic Stem Cell Transplantation in Multiple Sclerosis
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Ruder, Josefine, Rex, Jordan, Obahor, Simon, Docampo, María José, Müller, Antonia M S, Schanz, Urs, Jelcic, Ilijas, Martin, Roland, Ruder, Josefine, Rex, Jordan, Obahor, Simon, Docampo, María José, Müller, Antonia M S, Schanz, Urs, Jelcic, Ilijas, and Martin, Roland
- Abstract
Multiple sclerosis (MS) is an autoimmune disease of the central nervous system, in which autoreactive T and B cells play important roles. Other lymphocytes such as NK cells and innate-like T cells appear to be involved as well. To name a few examples, CD56bright NK cells were described as an immunoregulatory NK cell subset in MS while innate-like T cells in MS were described in brain lesions and with proinflammatory signatures. Autologous hematopoietic stem cell transplantation (aHSCT) is a procedure used to treat MS. This procedure includes hematopoietic stem/progenitor cell (HSPC) mobilization, then high-dose chemotherapy combined with anti-thymocyte globulin (ATG) and subsequent infusion of the patients own HSPCs to reconstitute a functional immune system. aHSCT inhibits MS disease activity very effectively and for long time, presumably due to elimination of autoreactive T cells. Here, we performed multidimensional flow cytometry experiments in peripheral blood lymphocytes of 27 MS patients before and after aHSCT to address its potential influence on NK and innate-like T cells. After aHSCT, the relative frequency and absolute numbers of CD56bright NK cells rise above pre-aHSCT levels while all studied innate-like T cell populations decrease. Hence, our data support an enhanced immune regulation by CD56bright NK cells and the efficient reduction of proinflammatory innate-like T cells by aHSCT in MS. These observations contribute to our current understanding of the immunological effects of aHSCT in MS.
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- 2021
144. Neuro-psychiatric manifestations in patients with systemic lupus erythematosus: A systematic review and results from the Swiss lupus cohort study
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Meier, Aline L; https://orcid.org/0000-0003-0698-711X, Bodmer, Nicolas S, Wirth, Carla, Bachmann, Lucas M, Ribi, Camillo, Pröbstel, Anne-Katrin, Waeber, David, Jelcic, Ilijas, Steiner, Urs C, Swiss SLE Cohort Study (SSCS), Meier, Aline L; https://orcid.org/0000-0003-0698-711X, Bodmer, Nicolas S, Wirth, Carla, Bachmann, Lucas M, Ribi, Camillo, Pröbstel, Anne-Katrin, Waeber, David, Jelcic, Ilijas, Steiner, Urs C, and Swiss SLE Cohort Study (SSCS)
- Abstract
OBJECTIVES Systemic lupus erythematosus (SLE) is a systemic autoimmune disease associated with neuro-psychiatric (NP) manifestations. Frequency and patterns of neuro-psychiatric systemic lupus erythematosus (NPSLE) vary substantially between patients. We conducted a systematic review (SR) of the literature and examined prevalence and characteristics of NPSLE in the Swiss SLE cohort study (SSCS). METHODS The SR search was performed between January 1999 and January 2020. We included prospective/cross-sectional studies focusing on NPSLE. We secured study characteristics, cohort compositions and frequencies of NP manifestations, assessed heterogeneity across reports and investigated sources of variation using meta-regression models. Regarding the SSCS, we reviewed all patients included and classified NP manifestations. RESULTS The SR searches identified 530 studies. We included 22 studies in our meta-analysis, the mean frequency of NPSLE ranged from 10.6% to 96.4%. The frequency of NPSLE in the SSCS was 28.1%. Severe events including cerebrovascular insults, seizures and psychosis appeared in 7.1%, 5.3% and 6.5% respectively. There was a linear relationship between duration of SLE and cumulative incidence of NPSLE. CONCLUSIONS The spectrum of NPSLE is very broad. The diagnostic work-up and rates of reported manifestations varied substantially across studies. We call for concerted efforts and consensus regarding definitions of NPSLE that will facilitate accurate diagnosis and attribution to SLE, particularly with a view to timely intervention and patient outcomes.
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- 2021
145. Autologous hematopoietic stem cell transplantation in multiple sclerosis: a global approval and availability review
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Stathopoulos, P, Léger, K, Foege, M, Lutterotti, A, Müller, A, Schanz, U, Jelcic, I; https://orcid.org/0000-0003-3090-7319, Martin, R; https://orcid.org/0000-0002-0982-1329, Stathopoulos, P, Léger, K, Foege, M, Lutterotti, A, Müller, A, Schanz, U, Jelcic, I; https://orcid.org/0000-0003-3090-7319, and Martin, R; https://orcid.org/0000-0002-0982-1329
- Published
- 2021
146. Thermal transmittance of a composite lightweight wall panel with integrated load-bearing structure: Experimental versus numerical approach
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Gaši, Mergim, Milovanović, Bojan, Tkalčić, Domagoj, and Rukavina, Marija Jelčić
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- 2023
- Full Text
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147. Clinical features and therapeutic outcomes of patients with acromegaly: Single-center experience
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Dusek, T., Kastelan, D., Melada, A., Baretic, M., Skoric Polovina, T., Perkovic, Z., Giljevic, Z., Jelcic, J., Paladino, J., Aganovic, I., and Korsic, M.
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- 2011
- Full Text
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148. Correction: Baričević et al. Cementitious Composites Reinforced with Waste Fibres from the Production of High-Quality Construction Textiles. Materials 2022, 15, 1611
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Marina Frančić Smrkić, Marija Jelcic Rukavina, Katarina Didulica, and Ana Baricevic
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General Materials Science - Abstract
In the original publication [...]
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- 2022
- Full Text
- View/download PDF
149. Simple motor stereotypies are not specific features of behavioural frontotemporal dementia
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Cagnin, Annachiara, Formentin, Chiara, Pompanin, Sara, Zarantonello, Giulia, Jelcic, Nela, Venneri, Annalena, and Ermani, Mario
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- 2014
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150. Hypercoagulability in Cushing’s syndrome: the role of specific haemostatic and fibrinolytic markers
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Kastelan, Darko, Dusek, Tina, Kraljevic, Ivana, Polasek, Ozren, Giljevic, Zlatko, Solak, Mirsala, Salek, Silva Zupancic, Jelcic, Jozo, Aganovic, Izet, and Korsic, Mirko
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- 2009
- Full Text
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