331 results on '"Molteni E"'
Search Results
102. Crystal structure of M. smegmatis DprE1 in complex with FAD and covalently bound BTZ043
- Author
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Neres, J., primary, Pojer, F., additional, Molteni, E., additional, Chiarelli, L., additional, Riccardi, G., additional, Mattevi, A., additional, Cole, S.T., additional, and Binda, C., additional
- Published
- 2012
- Full Text
- View/download PDF
103. From neurovascular coupling to neurovascular cascade: a study on neural, autonomic and vascular transients in attention
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Bari, V, primary, Calcagnile, P, additional, Molteni, E, additional, Re, R, additional, Contini, D, additional, Spinelli, L, additional, Caffini, M, additional, Torricelli, A, additional, Cubeddu, R, additional, Cerutti, S, additional, and Bianchi, A M, additional
- Published
- 2012
- Full Text
- View/download PDF
104. Inflammatory effects of Milan PM10: molecular pathways involved in the release of the cytokine IL-1β
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Camatini, M.C., primary, Molteni, E., additional, Bengalli, R., additional, Longhin, E., additional, and Gualtieri, M., additional
- Published
- 2011
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- View/download PDF
105. Study of neurovascular and autonomic response in a divided attention test by means of EEG, ECG and NIRS signals
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Bari, V., primary, Calcagnile, P., additional, Molteni, E., additional, Re, R., additional, Contini, D., additional, Spinelli, L., additional, Caffini, M., additional, Torricelli, A., additional, Cubeddu, R., additional, Cerutti, S., additional, and Bianchi, A. M., additional
- Published
- 2011
- Full Text
- View/download PDF
106. P17.7 EEG, fMRI, TMS and fNIRS: a comparison of different methods for brain mapping of cortical motor hand areas
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Visani, E., primary, Rossi Sebastiano, D., additional, Gilioli, I., additional, Granvillano, A., additional, Canafoglia, L., additional, Panzica, F., additional, Cubeddu, R., additional, Torricelli, A., additional, Spinelli, L., additional, Contini, D., additional, Caffini, M., additional, Zucchelli, L., additional, Molteni, E., additional, Bianchi, A.M., additional, Cerutti, S., additional, and Franceschetti, S., additional
- Published
- 2011
- Full Text
- View/download PDF
107. A methodological study for the multifactorial assessment of motor adaptation: Integration of kinematic and neural factors
- Author
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Molteni, E, primary, Preatoni, E, additional, Cimolin, V, additional, Bianchi, A M, additional, Galli, M, additional, and Rodano, R, additional
- Published
- 2010
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- View/download PDF
108. Moving dipoles method detects displacement in N2 and P3 generation in diffuse axonal injury patients
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Molteni, E, primary, Gatti, E, additional, Bianchi, A M, additional, and Cerutti, S, additional
- Published
- 2010
- Full Text
- View/download PDF
109. In vitro effects of summer and winter Milan particulate matter
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Gualtieri, M., primary, Longhin, E., additional, Pezzolato, E., additional, Mantecca, P., additional, Molteni, E., additional, Holme, J., additional, and Camatini, M., additional
- Published
- 2010
- Full Text
- View/download PDF
110. Liver stiffness values measured by transient elastography are increased in patients with acutely decompensated heart failure
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Pozzoni, P., primary, Prati, D., additional, Berzuini, A., additional, Gerosa, A., additional, Canovi, C., additional, Molteni, E., additional, Barbarini, M., additional, Bonino, F., additional, and Colli, A., additional
- Published
- 2009
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- View/download PDF
111. Frontal brain activation during a working memory task: a time-domain fNIRS study
- Author
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Molteni, E., primary, Baselli, G., additional, Bianchi, A. M., additional, Caffini, M., additional, Contini, D., additional, Spinelli, L., additional, Torricelli, A., additional, Cerutti, S., additional, and Cubeddu, R., additional
- Published
- 2009
- Full Text
- View/download PDF
112. Structural features and oxidative stress towards plasmidDNA of apramycin copper complex
- Author
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Balenci, D., primary, Bonechi, G., additional, D'Amelio, N., additional, Gaggelli, E., additional, Gaggelli, N., additional, Molteni, E., additional, Valensin, G., additional, Szczepanik, W., additional, Dziuba, M., additional, Święcicki, G., additional, and Jeżowska-Bojczuk, M., additional
- Published
- 2009
- Full Text
- View/download PDF
113. SPORADICA PRESENZA DI NOROVIRUS NEI PAZIENTI AFFETTI DA GASTROENTERITE
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Rimoldi, S.G., primary, Pagani, C., additional, Drago, L., additional, Lombardi, A., additional, Tocalli, L., additional, Molteni, E., additional, Bossi, C., additional, Tonielli, C., additional, and Gismondo, M.R., additional
- Published
- 2007
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114. TOWARDS AB INITIO CALCULATION OF THE CIRCULAR DICHROISM OF PEPTIDES.
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MOLTENI, E., ONIDA, G., and TIANA, G.
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CIRCULAR dichroism , *PEPTIDES , *OPTICAL spectra , *MOLECULAR conformation , *HYDROGEN bonding , *DIHEDRAL angles - Published
- 2012
115. Event related synchronization and Hilbert Huang transform in the study of motor adaptation: A comparison of methods.
- Author
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Molteni, E., Ferrari, M., Preatoni, E., Cimolin, V., Cerutti, S., and Bianchi, A.M.
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- 2011
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116. Proposal of a combined optoelectronic and electroencephalographic method for the study of kinematic and neural correlates of Motor Adaptation.
- Author
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Molteni, E., Preatoni, E., Cimolin, V., Bianchi, A.M., Rodano, R., Galli, M., and Cerutti, S.
- Published
- 2010
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- View/download PDF
117. Analysis of the dynamical behaviour of the EEG rhythms during a test of sustained attention.
- Author
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Molteni, E., Bianchi, A.M., Butti, M., Reni, G., and Zucca, C.
- Published
- 2007
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118. Molecular Characterization of a Variant of Proviral Bovine Leukaemia Virus (BLV)
- Author
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Molteni, E., primary, Agresti, A., additional, Meneveri, R., additional, Marozzi, A., additional, Malcovati, M., additional, Bonizzi, L., additional, Poli, G., additional, and Ginelli, E., additional
- Published
- 1996
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119. Applicability of DNA isolated from syncytiotrophoblast vesicles to gene amplification and molecular analysis
- Author
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Colucci, G., primary, Pesenti, E., additional, Molteni, E., additional, Lobbiani, A., additional, De Andreis, C., additional, Pariani, S., additional, Rossella, F., additional, Semprini, A. E., additional, and Simoni, G., additional
- Published
- 1993
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- View/download PDF
120. Structural features and oxidative stress towards plasmid DNA of apramycin copper complex.
- Author
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Balenci, D., Bonechi, G., D'Amelio, N., Gaggelli, E., Gaggelli, N., Molteni, E., Valensin, G., Szczepanik, W. W., Dziuba, M., Święcickib, G., and Jeżowska-Bojczuk, M.
- Subjects
MOLECULAR structure ,OXIDATIVE stress ,PLASMIDS ,DNA ,COPPER compounds ,METAL complexes ,HYDROGEN-ion concentration ,NUCLEAR magnetic resonance spectroscopy - Abstract
The interaction of apramycin with copper at different pH values was investigated by potentiometric titrations and EPR, UV-vis and CD spectroscopic techniques. The Cu(II)-apramycin complex prevailing at pH 6.5 was further characterized by NMR spectroscopy. Metal-proton distances derived from paramagnetic relaxation enhancements were used as restraints in a conformational search procedure in order to define the structure of the complex. Longitudinal relaxation rates were measured with the IR-COSY pulse sequence, thus solving the problems due to signal overlap. At pH 6.5 apramycin binds copper(II) with a 2 : 1 stoichiometry, through the vicinal hydroxyl and deprotonated amino groups of ring III. Plasmid DNA electrophoresis showed that the Cu(II)-apramycin complex is more active than free Cu(II) in generating strand breakages. Interestingly, this complex in the presence of ascorbic acid damages DNA with a higher yield than in the presence of H
2 O2 . [ABSTRACT FROM AUTHOR]- Published
- 2009
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121. Simvastatin treatment in subjects at high cardiovascular risk modulates AT1R expression on circulating monocytes and T lymphocytes.
- Author
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Marino F, Guasti L, Cosentino M, Rasini E, Ferrari M, Maio RC, Loraschi A, Cimpanelli MG, Schembri L, Legnaro M, Molteni E, Crespi C, Crema F, Venco A, and Lecchini S
- Published
- 2008
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122. [The Stresscath test in the diagnosis of urinary incontinence caused by incompetence of the bladder neck]
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Galli, Pa, Cerri, R, Molinaroli, Mc, Molteni, E, Molteni, B, Bucciero, A, and Genazzani, Andrea
- Subjects
Adult ,Urinary Bladder Neck Obstruction ,Parity ,Urinary Incontinence ,Pregnancy ,Infant, Newborn ,Birth Weight ,Humans ,Female ,Middle Aged ,Urinary Catheterization - Published
- 1987
123. A diffusion tensor MRI study of pediatric patients with severe non-traumatic brain injury
- Author
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Messina, R., Rocca, M. A., Pagani, E., Molteni, E., Strazzer, S., Boffa, G., Recla, M., Galbiati, S., Bardoni, A., Comi, G., and Massimo Filippi
124. Abnormalities of the attentional network following traumatic brain injury in pediatric patients: a fMRI study
- Author
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Rocca, M. A., Strazzer, S., Valsasina, P., Meo, E., Molteni, E., Recla, M., Susanna Galbiati, Bardoni, A., Comi, G., and Filippi, M.
125. Polysomnographic sleep patterns in pediatric unresponsive wakefulness syndrome: time-frequency characterization and prognostic value
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Molteni, E., Avantaggiato, P., Formica, F., Pastore, V., Katia Colombo, Arcieri, S., Arrigoni, F., Gigli, G. L., Valente, M., Lorenzut, S., Biase, S., and Strazzer, S.
126. COVID-19 due to the B.1.617.2 (Delta) variant compared to B.1.1.7 (Alpha) variant of SARS-CoV-2: a prospective observational cohort study
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Kläser, K., Molteni, E., Graham, M., Canas, L. S., Österdahl, M. F., Antonelli, M., Chen, L., Deng, J., Murray, B., Kerfoot, E., Wolf, J., May, A., Fox, B., Capdevila, J., Aanensen, D. M., Abudahab, K., Adams, H., Adams, A., Afifi, S., Aggarwal, D., Ahmad, S. S. Y., Aigrain, L., Alcolea-Medina, A., Alikhan, N-F, Allara, E., Amato, R., Angyal, A., Annett, T., Aplin, S., Ariani, C. V., Asad, H., Ash, A., Ashfield, P., Ashford, F., Atkinson, L., Attwood, S. W., Auckland, C., Aydin, A., Baker, D. J., Baker, P., Balcazar, C. E., Ball, J., Barrett, J. C., Barrow, M., Barton, E., Bashton, M., Bassett, A. R., Batra, R., Baxter, C., Bayzid, N., Beaver, C., Beckett, A. H., Beckwith, S. M., Bedford, L., Beer, R., Beggs, A., Bellis, K. L., Berry, L., Bertolusso, B., Best, A., Betteridge, E., Bibby, D., Bicknell, K., Binns, D., Birchley, A., Bird, P. W., Bishop, C., Blacow, R., Blakey, V., Blane, B., Bolt, F., Bonfield, J., Bonner, S., Bonsall, D., Boswell, T., Bosworth, A., Bourgeois, Y., Boyd, O., Bradley, D. T., Breen, C., Bresner, C., Breuer, J., Bridgett, S., Bronner, I. F., Brooks, E., Broos, A., Brown, J. R., Bucca, G., Buchan, S. L., Buck, D., Bull, M., Burns, P. J., Burton-Fanning, S., Byaruhanga, T., Byott, M., Campbell, S., Carabelli, A. M., Cargill, J. S., Carlile, M., Carvalho, S. F., Casey, A., Castigador, A., Catalan, J., Chalker, V., Chaloner, N. J., Chand, M., Chappell, J. G., Charalampous, T., Chatterton, W., Chaudhry, Y., Churcher, C. M., Clark, G., Clarke, P., Cogger, B. J., Cole, K., Collins, J., Colquhoun, R., Connor, T. R., Cook, K. F., Coombes, J., Corden, S., Cormie, C., Cortes, N., Cotic, M., Cotton, S., Cottrell, S., Coupland, L., Cox, M. G., Cox, A., Craine, N., Crawford, L., Cross, A., Crown, M. R., Crudgington, D., Cumley, N., Curran, T., Curran, M. D., da Silva Filipe, A., Dabrera, G., Darby, A. C., Davidson, R. K., Davies, A., Davies, R. M., Davis, T., de Angelis, D., De Lacy, E., de Oliveira Martins, L., de Silva, T. I., Debebe, J., Denton-Smith, R., Dervisevic, S., Dewar, R., Dey, J., Dias, J., Dobie, D., Dorman, M. J., Downing, F., Driscoll, M., du Plessis, L., Duckworth, N., Durham, J., Eastick, K., Easton, L. J., Eccles, R., Edgeworth, J., Edwards, S., Bouzidi, K. E., Eldirdiri, S., Ellaby, N., Elliott, S., Eltringham, G., Ensell, L., Erkiert, M. J., Zamudio, M. E., Essex, S., Evans, J. M., Evans, C., Everson, W., Fairley, D. J., Fallon, K., Fanaie, A., Farr, B. W., Fearn, C., Feltwell, T., Ferguson, L., Fina, L., Flaviani, F., Fleming, V. M., Forrest, S., Foster-Nyarko, E., Foulkes, B. H., Foulser, L., Fragakis, M., Frampton, D., Francois, S., Fraser, C., Freeman, T. M., Fryer, H., Fuchs, M., Fuller, W., Gajee, K., Galai, K., Gallagher, A., Gallagher, E., Gallagher, M. D., Gallis, M., Gaskin, A., Gatica-Wilcox, B., Geidelberg, L., Gemmell, M., Georgana, I., George, R. P., Gifford, L., Gilbert, L., Girgis, S. T., Glaysher, S., Goldstein, E. J., Golubchik, T., Gomes, A. N., Gonçalves, S., Goodfellow, I. G., Goodwin, S., Goudarzi, S., Gourtovaia, M., Graham, C. A., Graham, L., Grant, P. R., Green, L. R., Green, A., Greenaway, J., Gregory, R., Guest, M., Gunson, R. N., Gupta, R. K., Gutierrez, B., Haldenby, S. T., Hamilton, W. L., Hansford, S. E., Haque, T., Harris, K. A., Harrison, I., Harrison, E. M., Hart, J., Hartley, .J. A., Harvey, W. T., Harvey, M., Hassan-Ibrahim, M. O., Heaney, J., Helmer, T., Henderson, J. H., Hesketh, A. R., Hey, J., Heyburn, D., Higginson, E. E., Hill, V., Hill, J. D., Hilson, R. A., Hilvers, E., Holden, M. T. G., Hollis, A., Holmes, C. W., Holmes, N., Holmes, A. H., Hopes, R., Hornsby, H. R., Hosmillo, M., Houlihan, C., Howson-Wells, H. C., Hsu, S. N., Hubb, J., Huckson, H., Hughes, W., Hughes, J., Hughes, M., Hutchings, S., Idle, G, Illingworth, CJ, Impey, R, Irish-Tavares, D, Iturriza-Gomara, M, Izuagbe, R, Jackson, C, Jackson, B, Jackson, LM, Jackson, KA, Jackson, DK, Jahun, AS, James, V, James, K, Jeanes, C, Jeffries, AR, Jeremiah, S, Jermy, A, John, M, Johnson, R, Johnson, K, Johnston, I, Jones, O, Jones, S, Jones, H, Jones, CR, Jones, N, Joseph, A, Judges, S, Kay, GL, Kay, S, Keatley, J - P, Keeley, AJ, Kenyon, A, Kermack, LM, Khakh, M, Kidd, SP, Kimuli, M, Kirk, S, Kitchen, C, Kitchman, K, Knight, BA, Koshy, C, Kraemer, MUG, Kumziene-Summerhayes, S, Kwiatkowski, D, Lackenby, A, Laing, KG, Lampejo, T, Langford, CF, Lavin, D, Lawton, AI, Lee, JCD, Lee, D, Lensing, SV, Leonard, S, Levett, LJ, Le-Viet, T, Lewis, J, Lewis, K, Liddle, J, Liggett, S, Lillie, PJ, Lindsey, BB, Lister, MM, Livett, R, Lo, S, Loman, NJ, Loose, MW, Louka, SF, Loveson, KF, Lowdon, S, Lowe, H, Lowe, HL, Lucaci, AO, Ludden, C, Lynch, J, Lyons, RA, Lythgoe, K, Machin, NW, MacIntyre-Cockett, G, Mack, A, Macklin, B, Maclean, A, Macnaughton, E, Madona, P, Maes, M, Maftei, L, Mahanama, AIK, Mahungu, TW, Mair, D, Maksimovic, J, Malone, CS, Maloney, D, Manesis, N, Manley, R, Mantzouratou, A, Marchbank, A, Mariappan, A, Martincorena, I, Nunez, RTM, Mather, AE, Maxwell, P, Mayhew, M, Mbisa, T, McCann, CM, McCarthy, SA, McCluggage, K, McClure, PC, McCrone, JT, McHugh, MP, McKenna, JP, McKerr, C, McManus, GM, McMurray, CL, McMurray, C, McNally, A, Meadows, L, Medd, N, Megram, O, Menegazzo, M, Merrick, I, Michell, SL, Michelsen, ML, Mirfenderesky, M, Mirza, J, Miskelly, J, Moles-Garcia, E, Moll, RJ, Molnar, Z, Monahan, IM, Mondani, M, Mookerjee, S, Moore, C, Moore, J, Moore, N, Morcrette, H, Morgan, S, Morgan, M, Mori, M, Morriss, A, Moses, S, Mower, C, Muir, P, Mukaddas, A, Munemo, F, Munn, R, Murray, A, Murray, LJ, Murray, DR, Mutingwende, M, Myers, R, Nastouli, E, Nebbia, G, Nelson, A, Nelson, C, Nicholls, S, Nichols, J, Nicodemi, R, Nomikou, K, O’Grady, J, O’Brien, S, Odedra, M, Ohemeng-Kumi, N, Oliver, K, Orton, RJ, Osman, H, O’Toole, Á, Pacchiarini, N, Padgett, D, Page, AJ, Park, EJ, Park, NR, Parker, MD, Parmar, S, Partridge, DG, Pascall, D, Patel, A, Patel, B, Paterson, S, Payne, BAI, Peacock, SJ, Pearson, C, Pelosi, E, Percival, B, Perkins, J, Perry, M, Pinckert, ML, Platt, S, Podplomyk, O, Pohare, M, Pond, M, Pope, CF, Poplawski, R, Powell, J, Poyner, J, Prestwood, L, Price, A, Price, JR, Prieto, JA, Pritchard, DT, Prosolek, SJ, Pugh, G, Pusok, M, Pybus, OG, Pymont, HM, Quail, MA, Quick, J, Radulescu, C, Raghwani, J, Ragonnet-Cronin, M, Rainbow, L, Rajan, D, Rajatileka, S, Ramadan, NA, Rambaut, A, Ramble, J, Randell, PA, Randell, P, Ratcliffe, L, Raviprakash, V, Raza, M, Redshaw, NM, Rey, S, Reynolds, N, Richter, A, Robertson, DL, Robinson, E, Robson, SC, Rogan, F, Rooke, S, Rowe, W, Roy, S, Rudder, S, Ruis, C, Rushton, S, Ryan, F, Saeed, K, Samaraweera, B, Sambles, CM, Sanderson, R, Sanderson, T, Sang, F, Sass, T, Scher, E, Scott, G, Scott, C, Sehmi, J, Shaaban, S, Shah, D, Shaw, J, Shelest, E, Shepherd, JG, Sheridan, LA, Sheriff, N, Shirley, L, Sillitoe, J, Silviera, S, Simpson, DA, Singh, A, Singleton, D, Skvortsov, T, Sloan, TJ, Sluga, G, Smith, K, Smith, KS, Smith, P, Smith, DL, Smith, L, Smith, CP, Smith, N, Smollett, KL, Snell, LB, Somassa, T, Southgate, J, Spellman, K, Chapman, MHS, Spurgin, LG, Spyer, MJ, Stanley, R, Stanley, W, Stanton, TD, Starinskij, I, Stockton, J, Stonehouse, S, Storey, N, Studholme, DJ, Sudhanva, M, Swindells, E, Taha, Y, Tan, NK, Tang, JW, Tang, M, Taylor, BEW, Taylor, JF, Taylor, S, Temperton, B, Templeton, KE, Thomas, C, Thomson, L, Thomson, EC, Thornton, A, Thurston, SAJ, Todd, JA, Tomb, R, Tong, L, Tonkin-Hill, G, Torok, ME, Tovar-Corona, JM, Trebes, A, Trotter, AJ, Tsatsani, I, Turnbull, R, Turtle, L, Twohig, KA, Umpleby, H, Underwood, AP, Vamos, EE, Vasylyeva, TI, Vattipally, S, Vernet, G, Vipond, BB, Volz, EM, Walsh, S, Wang, D, Warne, B, Warwick-Dugdale, J, Wastnedge, E, Watkins, J, Watson, LK, Waugh, S, Webster, HJ, Weldon, D, Westwick, E, Whalley, T, Wheeler, H, Whitehead, M, Whiteley, M, Whitwham, A, Wierzbicki, C, Willford, NJ, Williams, L-A, Williams, R, Williams, C, Williams, CA, Williams, RJ, Williams, T, Williamson, KA, Wilson-Davies, E, Witele, E, Withell, KT, Witney, AA, Wolverson, P, Wong, N, Workman, T, Wright, V, Wright, DW, Wyatt, T, Wyllie, S, Xu-McCrae, L., Yavus, M., Yaze, G., Yeats, C. A., Yebra, G., Yew, W. C., Young, G. R., Young, J., Zarebski, A. E., Zhang, P., Modat, M., Hammers, A., Spector, T. D., Steves, C. J., Sudre, C. H., Ourselin, S., Duncan, E. L., Kläser, K., Molteni, E., Graham, M., Canas, L. S., Österdahl, M. F., Antonelli, M., Chen, L., Deng, J., Murray, B., Kerfoot, E., Wolf, J., May, A., Fox, B., Capdevila, J., Aanensen, D. M., Abudahab, K., Adams, H., Adams, A., Afifi, S., Aggarwal, D., Ahmad, S. S. Y., Aigrain, L., Alcolea-Medina, A., Alikhan, N-F, Allara, E., Amato, R., Angyal, A., Annett, T., Aplin, S., Ariani, C. V., Asad, H., Ash, A., Ashfield, P., Ashford, F., Atkinson, L., Attwood, S. W., Auckland, C., Aydin, A., Baker, D. J., Baker, P., Balcazar, C. E., Ball, J., Barrett, J. C., Barrow, M., Barton, E., Bashton, M., Bassett, A. R., Batra, R., Baxter, C., Bayzid, N., Beaver, C., Beckett, A. H., Beckwith, S. M., Bedford, L., Beer, R., Beggs, A., Bellis, K. L., Berry, L., Bertolusso, B., Best, A., Betteridge, E., Bibby, D., Bicknell, K., Binns, D., Birchley, A., Bird, P. W., Bishop, C., Blacow, R., Blakey, V., Blane, B., Bolt, F., Bonfield, J., Bonner, S., Bonsall, D., Boswell, T., Bosworth, A., Bourgeois, Y., Boyd, O., Bradley, D. T., Breen, C., Bresner, C., Breuer, J., Bridgett, S., Bronner, I. F., Brooks, E., Broos, A., Brown, J. R., Bucca, G., Buchan, S. L., Buck, D., Bull, M., Burns, P. J., Burton-Fanning, S., Byaruhanga, T., Byott, M., Campbell, S., Carabelli, A. M., Cargill, J. S., Carlile, M., Carvalho, S. F., Casey, A., Castigador, A., Catalan, J., Chalker, V., Chaloner, N. J., Chand, M., Chappell, J. G., Charalampous, T., Chatterton, W., Chaudhry, Y., Churcher, C. M., Clark, G., Clarke, P., Cogger, B. J., Cole, K., Collins, J., Colquhoun, R., Connor, T. R., Cook, K. F., Coombes, J., Corden, S., Cormie, C., Cortes, N., Cotic, M., Cotton, S., Cottrell, S., Coupland, L., Cox, M. G., Cox, A., Craine, N., Crawford, L., Cross, A., Crown, M. R., Crudgington, D., Cumley, N., Curran, T., Curran, M. D., da Silva Filipe, A., Dabrera, G., Darby, A. C., Davidson, R. K., Davies, A., Davies, R. M., Davis, T., de Angelis, D., De Lacy, E., de Oliveira Martins, L., de Silva, T. I., Debebe, J., Denton-Smith, R., Dervisevic, S., Dewar, R., Dey, J., Dias, J., Dobie, D., Dorman, M. J., Downing, F., Driscoll, M., du Plessis, L., Duckworth, N., Durham, J., Eastick, K., Easton, L. J., Eccles, R., Edgeworth, J., Edwards, S., Bouzidi, K. E., Eldirdiri, S., Ellaby, N., Elliott, S., Eltringham, G., Ensell, L., Erkiert, M. J., Zamudio, M. E., Essex, S., Evans, J. M., Evans, C., Everson, W., Fairley, D. J., Fallon, K., Fanaie, A., Farr, B. W., Fearn, C., Feltwell, T., Ferguson, L., Fina, L., Flaviani, F., Fleming, V. M., Forrest, S., Foster-Nyarko, E., Foulkes, B. H., Foulser, L., Fragakis, M., Frampton, D., Francois, S., Fraser, C., Freeman, T. M., Fryer, H., Fuchs, M., Fuller, W., Gajee, K., Galai, K., Gallagher, A., Gallagher, E., Gallagher, M. D., Gallis, M., Gaskin, A., Gatica-Wilcox, B., Geidelberg, L., Gemmell, M., Georgana, I., George, R. P., Gifford, L., Gilbert, L., Girgis, S. T., Glaysher, S., Goldstein, E. J., Golubchik, T., Gomes, A. N., Gonçalves, S., Goodfellow, I. G., Goodwin, S., Goudarzi, S., Gourtovaia, M., Graham, C. A., Graham, L., Grant, P. R., Green, L. R., Green, A., Greenaway, J., Gregory, R., Guest, M., Gunson, R. N., Gupta, R. K., Gutierrez, B., Haldenby, S. T., Hamilton, W. L., Hansford, S. E., Haque, T., Harris, K. A., Harrison, I., Harrison, E. M., Hart, J., Hartley, .J. A., Harvey, W. T., Harvey, M., Hassan-Ibrahim, M. O., Heaney, J., Helmer, T., Henderson, J. H., Hesketh, A. R., Hey, J., Heyburn, D., Higginson, E. E., Hill, V., Hill, J. D., Hilson, R. A., Hilvers, E., Holden, M. T. G., Hollis, A., Holmes, C. W., Holmes, N., Holmes, A. H., Hopes, R., Hornsby, H. R., Hosmillo, M., Houlihan, C., Howson-Wells, H. C., Hsu, S. N., Hubb, J., Huckson, H., Hughes, W., Hughes, J., Hughes, M., Hutchings, S., Idle, G, Illingworth, CJ, Impey, R, Irish-Tavares, D, Iturriza-Gomara, M, Izuagbe, R, Jackson, C, Jackson, B, Jackson, LM, Jackson, KA, Jackson, DK, Jahun, AS, James, V, James, K, Jeanes, C, Jeffries, AR, Jeremiah, S, Jermy, A, John, M, Johnson, R, Johnson, K, Johnston, I, Jones, O, Jones, S, Jones, H, Jones, CR, Jones, N, Joseph, A, Judges, S, Kay, GL, Kay, S, Keatley, J - P, Keeley, AJ, Kenyon, A, Kermack, LM, Khakh, M, Kidd, SP, Kimuli, M, Kirk, S, Kitchen, C, Kitchman, K, Knight, BA, Koshy, C, Kraemer, MUG, Kumziene-Summerhayes, S, Kwiatkowski, D, Lackenby, A, Laing, KG, Lampejo, T, Langford, CF, Lavin, D, Lawton, AI, Lee, JCD, Lee, D, Lensing, SV, Leonard, S, Levett, LJ, Le-Viet, T, Lewis, J, Lewis, K, Liddle, J, Liggett, S, Lillie, PJ, Lindsey, BB, Lister, MM, Livett, R, Lo, S, Loman, NJ, Loose, MW, Louka, SF, Loveson, KF, Lowdon, S, Lowe, H, Lowe, HL, Lucaci, AO, Ludden, C, Lynch, J, Lyons, RA, Lythgoe, K, Machin, NW, MacIntyre-Cockett, G, Mack, A, Macklin, B, Maclean, A, Macnaughton, E, Madona, P, Maes, M, Maftei, L, Mahanama, AIK, Mahungu, TW, Mair, D, Maksimovic, J, Malone, CS, Maloney, D, Manesis, N, Manley, R, Mantzouratou, A, Marchbank, A, Mariappan, A, Martincorena, I, Nunez, RTM, Mather, AE, Maxwell, P, Mayhew, M, Mbisa, T, McCann, CM, McCarthy, SA, McCluggage, K, McClure, PC, McCrone, JT, McHugh, MP, McKenna, JP, McKerr, C, McManus, GM, McMurray, CL, McMurray, C, McNally, A, Meadows, L, Medd, N, Megram, O, Menegazzo, M, Merrick, I, Michell, SL, Michelsen, ML, Mirfenderesky, M, Mirza, J, Miskelly, J, Moles-Garcia, E, Moll, RJ, Molnar, Z, Monahan, IM, Mondani, M, Mookerjee, S, Moore, C, Moore, J, Moore, N, Morcrette, H, Morgan, S, Morgan, M, Mori, M, Morriss, A, Moses, S, Mower, C, Muir, P, Mukaddas, A, Munemo, F, Munn, R, Murray, A, Murray, LJ, Murray, DR, Mutingwende, M, Myers, R, Nastouli, E, Nebbia, G, Nelson, A, Nelson, C, Nicholls, S, Nichols, J, Nicodemi, R, Nomikou, K, O’Grady, J, O’Brien, S, Odedra, M, Ohemeng-Kumi, N, Oliver, K, Orton, RJ, Osman, H, O’Toole, Á, Pacchiarini, N, Padgett, D, Page, AJ, Park, EJ, Park, NR, Parker, MD, Parmar, S, Partridge, DG, Pascall, D, Patel, A, Patel, B, Paterson, S, Payne, BAI, Peacock, SJ, Pearson, C, Pelosi, E, Percival, B, Perkins, J, Perry, M, Pinckert, ML, Platt, S, Podplomyk, O, Pohare, M, Pond, M, Pope, CF, Poplawski, R, Powell, J, Poyner, J, Prestwood, L, Price, A, Price, JR, Prieto, JA, Pritchard, DT, Prosolek, SJ, Pugh, G, Pusok, M, Pybus, OG, Pymont, HM, Quail, MA, Quick, J, Radulescu, C, Raghwani, J, Ragonnet-Cronin, M, Rainbow, L, Rajan, D, Rajatileka, S, Ramadan, NA, Rambaut, A, Ramble, J, Randell, PA, Randell, P, Ratcliffe, L, Raviprakash, V, Raza, M, Redshaw, NM, Rey, S, Reynolds, N, Richter, A, Robertson, DL, Robinson, E, Robson, SC, Rogan, F, Rooke, S, Rowe, W, Roy, S, Rudder, S, Ruis, C, Rushton, S, Ryan, F, Saeed, K, Samaraweera, B, Sambles, CM, Sanderson, R, Sanderson, T, Sang, F, Sass, T, Scher, E, Scott, G, Scott, C, Sehmi, J, Shaaban, S, Shah, D, Shaw, J, Shelest, E, Shepherd, JG, Sheridan, LA, Sheriff, N, Shirley, L, Sillitoe, J, Silviera, S, Simpson, DA, Singh, A, Singleton, D, Skvortsov, T, Sloan, TJ, Sluga, G, Smith, K, Smith, KS, Smith, P, Smith, DL, Smith, L, Smith, CP, Smith, N, Smollett, KL, Snell, LB, Somassa, T, Southgate, J, Spellman, K, Chapman, MHS, Spurgin, LG, Spyer, MJ, Stanley, R, Stanley, W, Stanton, TD, Starinskij, I, Stockton, J, Stonehouse, S, Storey, N, Studholme, DJ, Sudhanva, M, Swindells, E, Taha, Y, Tan, NK, Tang, JW, Tang, M, Taylor, BEW, Taylor, JF, Taylor, S, Temperton, B, Templeton, KE, Thomas, C, Thomson, L, Thomson, EC, Thornton, A, Thurston, SAJ, Todd, JA, Tomb, R, Tong, L, Tonkin-Hill, G, Torok, ME, Tovar-Corona, JM, Trebes, A, Trotter, AJ, Tsatsani, I, Turnbull, R, Turtle, L, Twohig, KA, Umpleby, H, Underwood, AP, Vamos, EE, Vasylyeva, TI, Vattipally, S, Vernet, G, Vipond, BB, Volz, EM, Walsh, S, Wang, D, Warne, B, Warwick-Dugdale, J, Wastnedge, E, Watkins, J, Watson, LK, Waugh, S, Webster, HJ, Weldon, D, Westwick, E, Whalley, T, Wheeler, H, Whitehead, M, Whiteley, M, Whitwham, A, Wierzbicki, C, Willford, NJ, Williams, L-A, Williams, R, Williams, C, Williams, CA, Williams, RJ, Williams, T, Williamson, KA, Wilson-Davies, E, Witele, E, Withell, KT, Witney, AA, Wolverson, P, Wong, N, Workman, T, Wright, V, Wright, DW, Wyatt, T, Wyllie, S, Xu-McCrae, L., Yavus, M., Yaze, G., Yeats, C. A., Yebra, G., Yew, W. C., Young, G. R., Young, J., Zarebski, A. E., Zhang, P., Modat, M., Hammers, A., Spector, T. D., Steves, C. J., Sudre, C. H., Ourselin, S., and Duncan, E. L.
- Abstract
The Delta (B.1.617.2) variant was the predominant UK circulating SARS-CoV-2 strain between May and December 2021. How Delta infection compares with previous variants is unknown. This prospective observational cohort study assessed symptomatic adults participating in the app-based COVID Symptom Study who tested positive for SARS-CoV-2 from May 26 to July 1, 2021 (Delta overwhelmingly the predominant circulating UK variant), compared (1:1, age- and sex-matched) with individuals presenting from December 28, 2020 to May 6, 2021 (Alpha (B.1.1.7) the predominant variant). We assessed illness (symptoms, duration, presentation to hospital) during Alpha- and Delta-predominant timeframes; and transmission, reinfection, and vaccine effectiveness during the Delta-predominant period. 3581 individuals (aged 18 to 100 years) from each timeframe were assessed. The seven most frequent symptoms were common to both variants. Within the first 28 days of illness, some symptoms were more common with Delta versus Alpha infection (including fever, sore throat, and headache) and some vice versa (dyspnoea). Symptom burden in the first week was higher with Delta versus Alpha infection; however, the odds of any given symptom lasting ≥ 7 days was either lower or unchanged. Illness duration ≥ 28 days was lower with Delta versus Alpha infection, though unchanged in unvaccinated individuals. Hospitalisation for COVID-19 was unchanged. The Delta variant appeared more (1.49) transmissible than Alpha. Re-infections were low in all UK regions. Vaccination markedly reduced the risk of Delta infection (by 69-84%). We conclude that COVID-19 from Delta or Alpha infections is similar. The Delta variant is more transmissible than Alpha; however, current vaccines showed good efficacy against disease. This research framework can be useful for future comparisons with new emerging variants. © 2022, The Author(s).
127. Infant's emotional variability associated to interactive stressful situation: a novel analysis approach with Sample Entropy and Lempel-Ziv Complexity.
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Montirosso R, Riccardi B, Molteni E, Borgatti R, and Reni G
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- 2010
- Full Text
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128. Passo dello strabismo: critica dell’arte e arte della critica
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stefano chiodi, Caterina Molteni e Martina Cavalli, and Chiodi, Stefano
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Storia dell'arte contemporanea ,Critica d'arte - Published
- 2022
129. Relationship between clone metrics and clinical outcome in clonal cytopenia
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Chiara Elena, Cinzia Sala, Martina Sarchi, Anna Gallì, Clara Camaschella, Mario Cazzola, Daniela Toniolo, Nicolas Fiorelli, Ettore Rizzo, Emanuela Boveri, Virginia Valeria Ferretti, Paolo Gasparini, Luca Malcovati, Sara Pozzi, Silvia Zibellini, Eulalia Catamo, Elisa Bono, Gabriele Todisco, Jacqueline Ferrari, Elisabetta Molteni, Galli, A., Todisco, G., Catamo, E., Sala, C., Elena, C., Pozzi, S., Bono, E., Ferretti, V. V., Rizzo, E., Molteni, E., Zibellini, S., Sarchi, M., Boveri, E., Ferrari, J., Fiorelli, N., Camaschella, C., Gasparini, P., Toniolo, D., Cazzola, M., and Malcovati, L.
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Adult ,Male ,Myeloid ,Immunology ,Clone (cell biology) ,clonal cytopenia ,Biology ,Biochemistry ,Myeloid Neoplasm ,DNA Methyltransferase 3A ,Cohort Studies ,Young Adult ,Gene Frequency ,medicine ,Humans ,Expressivity (genetics) ,Aged ,Aged, 80 and over ,Cytopenia ,clone metrics ,Cell Biology ,Hematology ,Middle Aged ,medicine.disease ,Phenotype ,medicine.anatomical_structure ,Dysplasia ,Mutation (genetic algorithm) ,Mutation ,clone metric ,Female ,Clonal Hematopoiesis - Abstract
Clonal cytopenia of undetermined significance (CCUS) is associated with an increased risk of developing a myeloid neoplasm with myelodysplasia (MN). To identify the features of the mutant clone(s) that is associated with clinical phenotype and progression, we studied the following cohorts of individuals: 311 patients with idiopathic cytopenia of undetermined significance (ICUS), 532 community-dwelling individuals without hematologic phenotype (n = 355) or with unexplained anemia (n = 177), and 592 patients with overt MN. Ninety-two of 311 (30%) patients with ICUS carried a somatic genetic lesion that signaled CCUS. Clonal hematopoiesis (CH) was detected in 19.7% and 27.7% of nonanemic and anemic community-dwelling individuals, respectively. Different mutation patterns and variant allele frequencies (VAFs) (clone metrics parameters) were observed in the conditions studied. Recurrent mutation patterns exhibited different VAFs associated with marrow dysplasia (0.17-0.48), indicating variable clinical expressivity of mutant clones. Unsupervised clustering analysis based on mutation profiles identified 2 major clusters, characterized by isolated DNMT3A mutations (CH-like cluster) or combinatorial mutation patterns (MN-like cluster), and showing different overall survival (HR, 1.8). In patients with CCUS, the 2 clusters had different risk of progression to MN (HR, 2.7). Within the MN-like cluster, distinct subsets with different risk of progression to MN were identified based on clone metrics. These findings unveil marked variability in the clinical expressivity of myeloid driver genes and underline the limitations of morphologic dysplasia for clinical staging of mutant hematopoietic clones. Clone metrics appears to be critical for informing clinical decision-making in patients with clonal cytopenia.
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- 2021
130. Fronto-temporal vulnerability to disconnection in paediatric moderate and severe traumatic brain injury
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Elena Beretta, Sandra Strazzer, Filippo Arrigoni, Giacomo Boffa, Massimo Filippi, Erika Molteni, Susanna Galbiati, Elisabetta Pagani, M A Rocca, Molteni, E., Pagani, E., Strazzer, S., Arrigoni, F., Beretta, E., Boffa, G., Galbiati, S., Filippi, M., and Rocca, M. A.
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Male ,medicine.medical_specialty ,Adolescent ,Traumatic brain injury ,Uncinate fasciculus ,Grey matter ,Corpus callosum ,behavioral disciplines and activities ,neurobehavioral sequelae ,Severity of Illness Index ,White matter ,03 medical and health sciences ,0302 clinical medicine ,Atrophy ,Internal medicine ,Fasciculus ,FIM scale ,Brain Injuries, Traumatic ,medicine ,Humans ,030212 general & internal medicine ,paediatric brain injury ,Gray Matter ,Child ,biology ,business.industry ,traumatic brain injury ,medicine.disease ,biology.organism_classification ,diffusion tensor imaging ,Magnetic Resonance Imaging ,White Matter ,medicine.anatomical_structure ,Diffusion Tensor Imaging ,nervous system ,Neurology ,Cardiology ,Female ,Neurology (clinical) ,Nerve Net ,business ,030217 neurology & neurosurgery ,Diffusion MRI - Abstract
Background: In patients with moderate and severe paediatric traumatic brain injury (TBI), we investigated the presence and severity of white matter (WM) tract damage, cortical lobar and deep grey matter (GM) atrophies, their interplay and their correlation with outcome rating scales. Methods: Diffusion tensor (DT) and 3D T1-weighted MRI scans were obtained from 22 TBI children (13 boys; mean age at insult=11.6years; 72.7% in chronic condition) and 31 age-matched healthy children. Patients were tested with outcome rating scales and the Wechsler Intelligence Scale for Children (WISC). DT MRIindices were obtained from several supra- and infra-tentorial WM tracts. Cortical lobar and deep GM volumes were derived. Comparisons between patients and controls, and between patients in acute (
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- 2018
131. A diffusion tensor magnetic resonance imaging study of paediatric patients with severe non-traumatic brain injury
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Massimiliano Copetti, Filippo Arrigoni, Massimo Filippi, Katia Colombo, Valentina Pastore, Erika Molteni, Sandra Strazzer, Giacomo Boffa, Maria A. Rocca, Elisabetta Pagani, Molteni, E, Rocca, Ma, Strazzer, S, Pagani, E, Colombo, K, Arrigoni, F, Boffa, G, Copetti, M, Pastore, V, and Filippi, Massimo
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Male ,Pathology ,medicine.medical_specialty ,Adolescent ,Statistics as Topic ,Corpus callosum ,Severity of Illness Index ,030218 nuclear medicine & medical imaging ,White matter ,03 medical and health sciences ,0302 clinical medicine ,Developmental Neuroscience ,Neural Pathways ,Fractional anisotropy ,Severity of illness ,Image Processing, Computer-Assisted ,medicine ,Humans ,Child ,Analysis of Variance ,medicine.diagnostic_test ,business.industry ,Glasgow Outcome Scale ,Minimally conscious state ,Magnetic resonance imaging ,medicine.disease ,White Matter ,Diffusion Magnetic Resonance Imaging ,medicine.anatomical_structure ,Brain Injuries ,Case-Control Studies ,Child, Preschool ,Pediatrics, Perinatology and Child Health ,Anisotropy ,Female ,Neurology (clinical) ,Psychology ,Nuclear medicine ,business ,030217 neurology & neurosurgery ,Diffusion MRI - Abstract
AimIn this observational study using 3T magnetic resonance imaging (MRI) and diffusion tensor, we investigated the differential effects of pathology, stage of disease, state of consciousness, and aetiology on the modifications of supra‐ and infra‐tentorial white matter tracts and their correlations with clinical scales in paediatric patients with severe non‐traumatic brain injury.MethodDiffusion tensor magnetic resonance imaging (DT‐MRI) was obtained from seven children with unresponsive wakefulness syndrome (UWS; five males, two females; age at event 5y; standard deviation [SD] 2y 1mo), six children in a minimally conscious state (MCS; three males, three females; age at event 5y 10mo; SD 5y), and 10 healthy children as controls(two males, eight females; age at study 10y 10mo; SD 2y 10mo). Fractional anisotropy, mean, axial, and radial diffusivities were calculated for the corpus callosum, inferior, middle (MCP), and superior cerebellar peduncles (SCP).ResultsDT‐MRI parameters from corpus callosum and SCP differed between patients and controls. MCP abnormalities were detected in patients presenting non‐traumatic composite aetiology (n=4) versus those suffering from pure anoxia (n=9). The supra‐tentorial compartment was more damaged (i.e. decreased fractional anisotropy and increased diffusivities) than the infra‐tentorial one. Correlations were found between DT‐MRI abnormalities and Glasgow Outcome Scale scores.InterpretationIn paediatric UWS/MCS, the severity of clinical disability correlates with white matter tract abnormalities.
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- 2017
132. The gigantic tooth of St. Christopher
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M Vergani, Michele Augusto Riva, E Molteni, Molteni, E, Vergani, M, and Riva, M
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History of medicine ,History ,MED/02 - STORIA DELLA MEDICINA ,MEDLINE ,Library science ,General Dentistry - Published
- 2019
133. Altered Recruitment of the Attention Network Is Associated with Disability and Cognitive Impairment in Pediatric Patients with Acquired Brain Injury
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Erika Molteni, Paola Valsasina, Susanna Galbiati, Ermelinda De Meo, Massimo Filippi, Sandra Strazzer, Alessandra Bardoni, Filippo Arrigoni, Maria A. Rocca, Monica Recla, Strazzer, S, Rocca, Ma, Molteni, E, De Meo, E, Recla, M, Valsasina, P, Arrigoni, F, Galbiati, S, Bardoni, A, and Filippi, Massimo
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Male ,Recruitment, Neurophysiological ,medicine.medical_specialty ,Article Subject ,Adolescent ,Pediatric acquired brain injury ,Poison control ,Diffuse Axonal Injury ,Neuroimaging ,Audiology ,Neuropsychological Tests ,behavioral disciplines and activities ,Gyrus Cinguli ,lcsh:RC321-571 ,Disability Evaluation ,Wisconsin Card Sorting Test ,Cerebellum ,medicine ,Humans ,Attention ,Child ,Acquired brain injury ,lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry ,medicine.diagnostic_test ,business.industry ,Diffuse axonal injury ,Cognition ,medicine.disease ,Functional Independence Measure ,Magnetic Resonance Imaging ,Neurology ,Brain Injuries ,Physical therapy ,Female ,Neurology (clinical) ,Nerve Net ,Functional magnetic resonance imaging ,business ,Cognition Disorders ,Research Article - Abstract
We assessed abnormalities of brain functional magnetic resonance imaging (fMRI) activity during a sustained attention task (Conners’ Continuous Performance Test (CCPT)) in 20 right-handed pediatric acquired brain injury (ABI) patients versus 7 right-handed age-matched healthy controls, and we estimated the correlation of such abnormalities with clinical and cognitive deficits. Patients underwent the Wechsler Intelligence Scale for Children (WISC), Wisconsin Card Sorting Test, and Functional Independence Measure (FIM) evaluations. During fMRI, patients and controls activated regions of the attention network. Compared to controls, ABI patients experienced a decreased average fMRI recruitment of the left cerebellum and a decreased deactivation of the left anterior cingulate cortex. With increasing task demand, compared to controls, ABI patients had an impaired ability to increase the recruitment of several posterior regions of the attention network. They also experienced a greater activation of frontal regions, which was correlated with worse performance on FIM, WISC, and fMRI CCPT. Such abnormal brain recruitment was significantly influenced by the type of lesion (focal versus diffuse axonal injury) and time elapsed from the event. Pediatric ABI patients experienced an inability to optimize attention network recruitment, especially when task difficulty was increased, which likely contributes to their clinical and cognitive deficits.
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- 2015
134. FNIRS measure of transitive and intransitive gesture execution, observation and imagination in ecological setting: A pilot study
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Maria Elide Vanutelli, Michela Balconi, Erika Molteni, Livia Cortesi, Vanutelli, M, Cortesi, L, Molteni, E, and Balconi, M
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Imagination ,cognition ,Adult ,Male ,Settore M-PSI/02 - PSICOBIOLOGIA E PSICOLOGIA FISIOLOGICA ,media_common.quotation_subject ,Movement ,Posterior parietal cortex ,Pilot Projects ,functional nir ,M-PSI/02 - PSICOBIOLOGIA E PSICOLOGIA FISIOLOGICA ,imitation ,Hemoglobins ,Random Allocation ,Motor imagery ,motor imagery ,Near-infrared spectroscopy ,Humans ,hand action ,movements ,Set (psychology) ,infrared spectroscopy ,Ecosystem ,media_common ,Transitive relation ,haemodynamics ,Spectroscopy, Near-Infrared ,Gestures ,Ecology ,Brain ,Cognition ,simulation ,Nontherapeutic Human Experimentation ,tool use ,parietal cortex ,brain models ,Female ,activation ,Sensorimotor Cortex ,bio-optics ,Psychology ,M-PSI/01 - PSICOLOGIA GENERALE ,Gesture - Abstract
To explore the presence of differential cortical hemodynamic activations related to cognitive components of actions, we performed a fNIRS (functional Near-Infrared Spectroscopy) study during Observation (O), Execution (E) and Imagination (I) of complex and meaningful (transitive and intransitive) gestures in ecological setting. A pilot sample of 5 healthy adults underwent an event-related study consisting of these 3 different conditions, with O set as first and followed by a randomized presentation of E or I. fNIRS measurements were performed using a 24 channel array of optodes (8 light injectors and 8 detectors) placed over the contralateral central, centro-parietal, parietal and temporal areas. Results showed that the premotor (PMC) and the sensory-motor cortices (SM1) were recruited selectively during E, with levels of oxygenated hemoglobin (oxy-Hb) higher than the other conditions, while the posterior parietal cortex (PPC) showed increased oxy-Hb levels for both E and O. These data suggest that variations in hemodynamic responses can be attributed to different neural processes underpinning these tasks, with PMC and SM1 being more involved in action preparation and performance, and PPC prevalently dedicated to attentive processes related to the execution and observation of limb movements.
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- 2015
135. Release of IL-1 β triggered by milan Summer PM10: Molecular pathways involved in the cytokine release
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Rossella Bengalli, Magne Refsnes, Elisabetta Molteni, Eleonora Longhin, Marina Camatini, Maurizio Gualtieri, Gualtieri, M., Bengalli, R, Molteni, E, Longhin, E, Refsnes, M, Camatini, M, and Gualtieri, M
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Lipopolysaccharides ,Macrophage ,Immunology and Microbiology (all) ,medicine.medical_treatment ,Interleukin-1beta ,lcsh:Medicine ,Monocyte ,Monocytes ,Endosome ,Receptor ,Air Pollutants ,Endocytosi ,Caspase 1 ,VDP::Medisinske fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Toksikologi: 730 ,Interleukin ,Inflammasome ,General Medicine ,Caspase Inhibitors ,Endocytosis ,Cell biology ,Cytokine ,Italy ,Air Pollutant ,Seasons ,medicine.symptom ,Reactive Oxygen Specie ,Research Article ,medicine.drug ,Human ,Article Subject ,Inflammation ,Lipopolysaccharide ,Endosomes ,Biology ,General Biochemistry, Genetics and Molecular Biology ,Proinflammatory cytokine ,Cell Line ,VDP::Midical sciences: 700::Basic medical, dental and veterinary sciences: 710::Toxicology: 730 ,medicine ,Humans ,Biochemistry, Genetics and Molecular Biology (all) ,General Immunology and Microbiology ,Macrophages ,lcsh:R ,Oxidative Stre ,Toll-Like Receptor 2 ,Culture Media ,Toll-Like Receptor 4 ,Oxidative Stress ,Caspase Inhibitor ,Particulate Matter ,Season ,Reactive Oxygen Species - Abstract
Particulate matter (PM) exposure is related to pulmonary and cardiovascular diseases, with increased inflammatory status. The release of the proinflammatory interleukin- (IL-) 1β, is controlled by a dual pathway, the formation of inactive pro-IL-1β, through Toll-like receptors (TLRs) activation, and its cleavage by NLRP3 inflammasome. THP-1-derived macrophages were exposed for 6 h to 2.5 μg/cm2of Milan PM10, and the potential to promote IL-1βrelease by binding TLRs and activating NLRP3 has been examined. Summer PM10, induced a marked IL-1βresponse in the absence of LPS priming (50-fold increase compared to unexposed cells), which was reduced by caspase-1 inhibition (91% of inhibition respect summer PM10-treated cells) and by TLR-2 and TLR-4 inhibitors (66% and 53% of inhibition, resp.). Furthermore, summer PM10increased the number of early endosomes, and oxidative stress inhibition nearly abolished PM10-induced IL-1βresponse (90% of inhibition). These findings suggest that summer PM10contains constituents both related to the activation of membrane TLRs and activation of the inflammasome NLPR3 and that TLRs activation is of pivotal importance for the magnitude of the response. ROS formation seems important for PM10-induced IL-1βresponse, but further investigations are needed to elucidate the molecular pathway by which this effect is mediated.
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- 2013
136. In vitro effects of summer and winter Milan particulate matter
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Paride Mantecca, E. Pezzolato, Eleonora Longhin, E. Molteni, Marina Camatini, Maurizio Gualtieri, Jørn A. Holme, Gualtieri, M, Longhin, E, Pezzolato, E, Mantecca, P, Molteni, E, Holme, J, and Camatini, M
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Environmental chemistry ,General Medicine ,Biology ,Particulates ,PM1, PM2.5, seasonal ,Toxicology ,BIO/06 - ANATOMIA COMPARATA E CITOLOGIA - Abstract
Introduction: The high concentration of particulate matter (PM10, PM2.5 and PM1) in Milan is a cause of health concern. This study investigates the biological effects of PM10, PM2.5 and PM1 sampled in Milan during summer and winter seasons for the evidence of a seasonal difference in PMs chemical and microbiological composition. Results: The winter PMs presented higher levels of PAHs in comparison to the summer ones, which contained a greater amount of mineral dust elements and biological components such as gram-negative bacteria (LAL test). PM biological effects were analysed on the human bronchial epithelial cell line BEAS-2B and the monocytes cell line THP-1. Winter PMs were toxic in BEAS-2B and THP-1 as assessed by PI/Hoechst staining, while summer PMs induced a higher pro-inflammatory response. Summer PM10 induced IL-8 release in both the cell lines. Interestingly summer PM10 induced in THP-1 cells an increase in IL-1b expression. Moreover winter PMs were able to induce a G2/M arrest in BEAS-2B and THP-1 cell cycle. Conclusions: These results evidence a correlation between the PM chemical/biogenic composition and the biological effects. The higher content of LPS deriving from the gram-negative bacteria correlates with the higher pro-inflammatory potency of the summer PMs, while the higher content of PAHs in winter might be responsible for the increased cytotoxicity and cell cycle arrest
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- 2010
137. Qualitative exploration of the lived experiences of loneliness in later life to inform technology development.
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Rees J, Liu W, Canson J, Crosby L, Tinker A, Probst F, Ourselin S, Antonelli M, Molteni E, Mexia N, Shi Y, and Matcham F
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- Humans, Aged, Female, Male, Aged, 80 and over, Interviews as Topic, Loneliness psychology, Qualitative Research
- Abstract
Purpose: Loneliness is a negative emotional state which is common in later life. The accumulative effects of loneliness have a significant impact on the physical and mental health of older adults. We aim to qualitatively explore the experiences of loneliness in later life and identify relevant behaviours and indicators which will inform novel methods of loneliness detection and intervention., Methods: We conducted 60 semi-structured interviews with people aged 65 and over between September 2022 and August 2023. Data were analysed using a reflective thematic approach with early theme development on NVIVO software., Results: Three themes were identified from the experiences of loneliness in older adults. 1) Unique responses to loneliness, including crying, increased eating or drinking and sleep difficulties, 2) Age-related losses, such as networks, roles, and abilities to engage in activities reducing over time and 3) Individual differences in overcoming loneliness, where strategies such as keeping busy and adopting a positive mindset were impacted by motivation and mood of older adults., Conclusion: Distinct signs and relevant factors to loneliness in later life have been identified which can be detected by future sensing technologies. Findings of this in-depth qualitative study highlight that loneliness is a subjective experience requiring a holistic and person-centred approach to detection and intervention.
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- 2024
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138. Correction: Common Data Elements for Disorders of Consciousness: Recommendations from the Working Group in the Pediatric Population.
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Boerwinkle VL, Appavu B, Cediel EG, Erklaurer J, Lalgudi Ganesan S, Gibbons C, Hahn C, LaRovere KL, Moberg D, Natarajan G, Molteni E, Reuther WR, and Slomine BS
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- 2024
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139. Is ctDNA ready to outpace imaging in monitoring early and advanced breast cancer?
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Foffano L, Vida R, Piacentini A, Molteni E, Cucciniello L, Da Ros L, Silvia B, Cereser L, Roncato R, Gerratana L, and Puglisi F
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- Humans, Female, Liquid Biopsy methods, Precision Medicine methods, Neoplasm Recurrence, Local, Biomarkers, Tumor genetics, Diagnostic Imaging methods, Breast Neoplasms diagnosis, Breast Neoplasms genetics, Breast Neoplasms pathology, Circulating Tumor DNA, Disease Progression
- Abstract
Introduction: Circulating tumor DNA (ctDNA) and radiological imaging are increasingly recognized as crucial elements in breast cancer management. While radiology remains the cornerstone for screening and monitoring, ctDNA holds distinctive advantages in anticipating diagnosis, recurrence, or progression, providing concurrent biological insights complementary to imaging results., Areas Covered: This review delves into the current evidence on the synergistic relationship between ctDNA and imaging in breast cancer. It presents data on the clinical validity and utility of ctDNA in both early and advanced settings, providing insights into emerging liquid biopsy techniques like epigenetics and fragmentomics. Simultaneously, it explores the present and future landscape of imaging methodologies, particularly focusing on radiomics., Expert Opinion: Numerous are the current technical, strategic, and economic challenges preventing the clinical integration of ctDNA analysis in the breast cancer monitoring. Understanding these complexities and devising targeted strategies is pivotal to effectively embedding this methodology into personalized patient care.
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- 2024
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140. Brain-Computer Interfaces for Communication in Patients with Disorders of Consciousness: A Gap Analysis and Scientific Roadmap.
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Schiff ND, Diringer M, Diserens K, Edlow BL, Gosseries O, Hill NJ, Hochberg LR, Ismail FY, Meyer IA, Mikell CB, Mofakham S, Molteni E, Polizzotto L, Shah SA, Stevens RD, and Thengone D
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- Humans, Communication, Brain-Computer Interfaces, Consciousness Disorders physiopathology, Consciousness Disorders therapy
- Abstract
Background: We developed a gap analysis that examines the role of brain-computer interfaces (BCI) in patients with disorders of consciousness (DoC), focusing on their assessment, establishment of communication, and engagement with their environment., Methods: The Curing Coma Campaign convened a Coma Science work group that included 16 clinicians and neuroscientists with expertise in DoC. The work group met online biweekly and performed a gap analysis of the primary question., Results: We outline a roadmap for assessing BCI readiness in patients with DoC and for advancing the use of BCI devices in patients with DoC. Additionally, we discuss preliminary studies that inform development of BCI solutions for communication and assessment of readiness for use of BCIs in DoC study participants. Special emphasis is placed on the challenges posed by the complex pathophysiologies caused by heterogeneous brain injuries and their impact on neuronal signaling. The differences between one-way and two-way communication are specifically considered. Possible implanted and noninvasive BCI solutions for acute and chronic DoC in adult and pediatric populations are also addressed., Conclusions: We identify clinical and technical gaps hindering the use of BCI in patients with DoC in each of these contexts and provide a roadmap for research aimed at improving communication for adults and children with DoC, spanning the clinical spectrum from intensive care unit to chronic care., (© 2024. Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society.)
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- 2024
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141. Symptoms before and after COVID-19: a population and case-control study using prospective data.
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Sudre CH, Antonelli M, Cheetham NJ, Molteni E, Canas LS, Bowyer V, Murray B, Rjoob K, Modat M, Capdevila Pujol J, Hu C, Wolf J, Spector TD, Hammers A, Steves CJ, Ourselin S, and Duncan EL
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- Humans, Female, Male, Case-Control Studies, Middle Aged, Prospective Studies, Adult, Aged, Time Factors, Post-Acute COVID-19 Syndrome, Survival Analysis, Fatigue epidemiology, COVID-19 epidemiology, COVID-19 complications, SARS-CoV-2
- Abstract
Background: Some individuals experience prolonged illness after acute coronavirus disease 2019 (COVID-19). We assessed whether pre-infection symptoms affected post-acute COVID illness duration., Methods: Survival analysis was performed in adults (n=23 452) with community-managed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection prospectively self-logging data through the ZOE COVID Symptom Study app, at least weekly, from 8 weeks before to 12 weeks after COVID-19 onset, conditioned on presence versus absence of baseline symptoms (4-8 weeks before COVID-19). A case-control study was performed in 1350 individuals with long illness (≥8 weeks, including 906 individuals (67.1%) with illness ≥12 weeks), matched 1:1 (for age, sex, body mass index, testing week, prior infection, vaccination, smoking, index of multiple deprivation) with 1350 individuals with short illness (<4 weeks). Baseline symptoms were compared between the two groups, and against post-COVID symptoms., Results: Individuals reporting baseline symptoms had longer COVID-related symptom duration (median 15 days versus 10 days for individuals without baseline symptoms) with baseline fatigue nearly doubling duration. Two-thirds (910 (67.4%) of 1350) of individuals with long illness were asymptomatic beforehand. However, 440 (32.6%) had baseline symptoms, versus 255 (18.9%) of 1350 individuals with short illness (p<0.0001). Baseline symptoms doubled the odds ratio for long illness (2.14, 95% CI 1.78-2.57). Prior comorbidities were more common in individuals with long versus short illness. In individuals with long illness, baseline symptomatic ( versus asymptomatic) individuals were more likely to be female, younger, and have prior comorbidities; and baseline and post-acute symptoms, and symptom burden, correlated strongly., Conclusions: Individuals experiencing symptoms before COVID-19 had longer illness duration and increased odds of long illness. However, many individuals with long illness were well before SARS-CoV-2 infection., Competing Interests: Conflict of interest: T.D. Spector and J. Wolf are co-founders and founder shareholders of ZOE Ltd. C. Hu and J. Capdevila Pujol are employees of ZOE Ltd. C.J. Steves and S. Ourselin have consulted for ZOE Ltd. All other authors (M. Antonelli, C.H. Sudre, E. Molteni, L.S. Canas, N.J. Cheetham, A. Hammers, E.L. Duncan, V. Bowyer, K. Rjoob, M. Modat and B. Murray) declare no conflict of interest., (Copyright ©The authors 2024.)
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- 2024
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142. Ab Initio Electronic, Magnetic, and Optical Properties of Fe Phthalocyanine on Cr 2 O 3 (0001).
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Marino M, Molteni E, Achilli S, Onida G, and Fratesi G
- Abstract
The organic molecules adsorbed on antiferromagnetic surfaces can produce interesting interface states, characterized by charge transfer mechanisms, hybridization of molecular-substrate orbitals, as well as magnetic couplings. Here, we apply an ab initio approach to study the adsorption of Fe phthalocyanine on stoichiometric Cr
2 O3 (0001). The molecule binds via a bidentate configuration forming bonds between two opposite imide N atoms and two protruding Cr ones, making this preferred over the various possible adsorption structures. In addition to the local modifications at these sites, the electronic structure of the molecule is weakly influenced. The magnetic structure of the surface Cr atoms shows a moderate influence of molecule adsorption, not limited to the atoms in the close proximity of the molecule. Upon optical excitation at the onset, electron density moves toward the molecule, enhancing the ground state charge transfer. We investigate this movement of charge as a mechanism at the base of light-induced modifications of the magnetic structure at the interface.- Published
- 2024
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143. Enhancement of Magnetic Stability in Antiferromagnetic CoO Films by Adsorption of Organic Molecules.
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Gnoli L, Benini M, Del Conte C, Riminucci A, Rakshit RK, Singh M, Sanna S, Yadav R, Lin KW, Mezzi A, Achilli S, Molteni E, Marino M, Fratesi G, Dediu V, and Bergenti I
- Abstract
Antiferromagnets are a class of magnetic materials of great interest in spintronic devices because of their stability and ultrafast dynamics. When interfaced with an organic molecular layer, antiferromagnetic (AF) films are expected to form a spinterface that can allow fine control of specific AF properties. In this paper, we investigate spinterface effects on CoO, an AF oxide. To access the magnetic state of the antiferromagnet, we couple it to a ferromagnetic Co film via an exchange bias (EB) effect. In this way, the formation of a spinterface is detected through changes induced on the CoO/Co EB system. We demonstrate that C
60 and Gaq3 adsorption on CoO shifts its blocking temperature; in turn, an increase in both the EB fields and the coercivities is observed on the EB-coupled Co layer. Ab initio calculations for the CoO/C60 interface indicate that the molecular adsorption is responsible for a charge redistribution on the CoO layer that alters the occupation of the d orbitals of Co atoms and, to a smaller extent, the p orbitals of oxygen. As a result, the AF coupling between Co atoms in the CoO is enhanced. Considering the granular nature of CoO, a larger AF stability upon molecular adsorption is then associated with a larger number of AF grains that are stable upon reversal of the Co layer., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)- Published
- 2024
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144. Novel insights into the management of rheumatoid arthritis: one year in review 2024.
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Molteni E, Adinolfi A, Bondi V, Delvino P, Sakellariou G, Trentanni C, Ughi N, Pozzi MR, and Scirè CA
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- Humans, Remission Induction, Treatment Outcome, Arthritis, Rheumatoid drug therapy, Antirheumatic Agents therapeutic use, Glucocorticoids therapeutic use, Janus Kinase Inhibitors therapeutic use
- Abstract
New evidence from 2023 has slightly shifted some perspectives on rheumatoid arthritis (RA) management. Glucocorticoids have reaffirmed their role as bridging therapy, while novel studies on JAK inhibitors have examined efficacy, mechanism of action, and their potential in high-risk populations, bolstering our understanding with real-world data.Additionally, among treatment strategies, achieving low disease activity has emerged as comparable to achieving remission in the long term, and new insights have been gained regarding tapering both biological and conventional synthetic DMARDs. Furthermore, novel approaches have been proposed for managing difficult-to-treat RA and pre-RA. In this paper, the reviewers aim to present the most relevant studies published during the last year in the field of RA management.
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- 2024
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145. Dihydrotanshinone I exhibits antitumor effects via β-catenin downregulation in papillary thyroid cancer cell lines.
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Molteni E, Baldan F, Damante G, and Allegri L
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- Humans, Thyroid Cancer, Papillary drug therapy, Thyroid Cancer, Papillary pathology, beta Catenin genetics, beta Catenin metabolism, Down-Regulation, Cell Line, Tumor, Wnt Signaling Pathway genetics, Cell Proliferation physiology, Cell Movement genetics, Carcinoma, Papillary drug therapy, Carcinoma, Papillary genetics, Carcinoma, Papillary metabolism, Thyroid Neoplasms drug therapy, Thyroid Neoplasms genetics, Thyroid Neoplasms metabolism, Furans, Phenanthrenes, Quinones
- Abstract
Thyroid cancer is the most common endocrine carcinoma and, among its different subtypes, the papillary subtype (PTC) is the most frequent. Generally, PTCs are well differentiated, but a minor percentage of PTCs are characterized by a worse prognosis and more aggressive behavior. Phytochemicals, naturally found in plant products, represent a heterogeneous group of bioactive compounds that can interfere with cell proliferation and the regulation of the cell cycle, taking part in multiple signaling pathways that are often disrupted in tumor initiation, proliferation, and progression. In this work, we focused on 15,16-dihydrotanshinone I (DHT), a tanshinone isolated from Salvia miltiorrhiza Bunge (Danshen). We first evaluated DHT biological effect on PTC cells regarding cell viability, colony formation ability, and migration capacity. All of these parameters were downregulated by DHT treatment. We then investigated gene expression changes after DHT treatment by performing RNA-seq. The analysis revealed that DHT significantly reduced the Wnt signaling pathway, which plays a role in various diseases, including cancer. Finally, we demonstrate that DHT treatment decreases protein levels of β-catenin, a final effector of canonical Wnt signaling pathway. Overall, our data suggest a possible use of this nutraceutical as an adjuvant in the treatment of aggressive papillary thyroid carcinoma., (© 2024. The Author(s).)
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- 2024
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146. Treatments and Outcomes Among Patients with Sydenham Chorea: A Meta-Analysis.
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Eyre M, Thomas T, Ferrarin E, Khamis S, Zuberi SM, Sie A, Newlove-Delgado T, Morton M, Molteni E, Dale RC, Lim M, and Nosadini M
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- Humans, Female, Child, Male, Treatment Outcome, Adolescent, Recurrence, Chorea drug therapy, Chorea therapy
- Abstract
Importance: Sydenham chorea is the most common acquired chorea of childhood worldwide; however, treatment is limited by a lack of high-quality evidence., Objectives: To evaluate historical changes in the clinical characteristics of Sydenham chorea and identify clinical and treatment factors at disease onset associated with chorea duration, relapsing disease course, and functional outcome., Data Sources: The systematic search for this meta-analysis was conducted in PubMed, Embase, CINAHL, Cochrane Library, and LILACS databases and registers of clinical trials from inception to November 1, 2022 (search terms: [Sydenham OR Sydenham's OR rheumatic OR minor] AND chorea)., Study Selection: Published articles that included patients with a final diagnosis of Sydenham chorea (in selected languages)., Data Extraction and Synthesis: This study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. Individual patient data on clinical characteristics, treatments, chorea duration, relapse, and final outcome were extracted. Data from patients in the modern era (1945 through 2022) were entered into multivariable models and stratified by corticosteroid duration for survival analysis of chorea duration., Main Outcomes and Measures: The planned study outcomes were chorea duration at onset, monophasic course (absence of relapse after ≥24 months), and functional outcome (poor: modified Rankin Scale score 2-6 or persisting chorea, psychiatric, or behavioral symptoms at final follow-up after ≥6 months; good: modified Rankin Scale score 0-1 and no chorea, psychiatric, or behavioral symptoms at final follow-up)., Results: In total, 1479 patients were included (from 307 articles), 1325 since 1945 (median [IQR] age at onset, 10 [8-13] years; 875 of 1272 female [68.8%]). Immunotherapy was associated with shorter chorea duration (hazard ratio for chorea resolution, 1.51 [95% CI, 1.05-2.19]; P = .03). The median chorea duration in patients receiving 1 or more months of corticosteroids was 1.2 months (95% CI, 1.2-2.0) vs 2.8 months (95% CI, 2.0-3.0) for patients receiving none (P = .004). Treatment factors associated with monophasic disease course were antibiotics (odds ratio [OR] for relapse, 0.28 [95% CI, 0.09-0.85]; P = .02), corticosteroids (OR, 0.32 [95% CI, 0.15-0.67]; P = .003), and sodium valproate (OR, 0.33 [95% CI, 0.15-0.71]; P = .004). Patients receiving at least 1 month of corticosteroids had significantly lower odds of relapsing course (OR, 0.10 [95% CI, 0.04-0.25]; P < .001). No treatment factor was associated with good functional outcome., Conclusions and Relevance: In this meta-analysis of treatments and outcomes in patients with Sydenham chorea, immunotherapy, in particular corticosteroid treatment, was associated with faster resolution of chorea. Antibiotics, corticosteroids and sodium valproate were associated with a monophasic disease course. This synthesis of retrospective data should support the development of evidence-based treatment guidelines for patients with Sydenham chorea.
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- 2024
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147. Common Data Elements for Disorders of Consciousness: Recommendations from the Working Group in the Pediatric Population.
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Boerwinkle VL, Appavu B, Cediel EG, Erklaurer J, Lalgudi Ganesan S, Gibbons C, Hahn C, LaRovere KL, Moberg D, Natarajan G, Molteni E, Reuther WR, and Slomine BS
- Subjects
- Infant, Newborn, Humans, Child, Consciousness, Coma diagnosis, Coma therapy, Consciousness Disorders diagnosis, Consciousness Disorders therapy, Common Data Elements, Biomedical Research
- Abstract
Background: The fundamental gap obstructing forward progress of evidenced-based care in pediatric and neonatal disorders of consciousness (DoC) is the lack of defining consensus-based terminology to perform comparative research. This lack of shared nomenclature in pediatric DoC stems from the inherently recursive dilemma of the inability to reliably measure consciousness in the very young. However, recent advancements in validated clinical examinations and technologically sophisticated biomarkers of brain activity linked to future abilities are unlocking this previously formidable challenge to understanding the DoC in the developing brain., Methods: To address this need, the first of its kind international convergence of an interdisciplinary team of pediatric DoC experts was organized by the Neurocritical Care Society's Curing Coma Campaign. The multidisciplinary panel of pediatric DoC experts proposed pediatric-tailored common data elements (CDEs) covering each of the CDE working groups including behavioral phenotyping, biospecimens, electrophysiology, family and goals of care, neuroimaging, outcome and endpoints, physiology and big Data, therapies, and pediatrics., Results: We report the working groups' pediatric-focused DoC CDE recommendations and disseminate CDEs to be used in studies of pediatric patients with DoC., Conclusions: The CDEs recommended support the vision of progressing collaborative and successful internationally collaborative pediatric coma research., (© 2023. Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society.)
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- 2024
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148. Common Data Element for Disorders of Consciousness: Recommendations from the Working Group on Therapeutic Interventions.
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Monti MM, Beekman R, Spivak NM, Thibaut A, Schnakers C, Whyte J, and Molteni E
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- Humans, Consciousness, Consciousness Disorders diagnosis, Consciousness Disorders therapy, Common Data Elements, Biomedical Research
- Abstract
Background: Over the past 30 years, there have been significant advances in the understanding of the mechanisms associated with loss and recovery of consciousness following severe brain injury. This work has provided a strong grounding for the development of novel restorative therapeutic interventions. Although all interventions are aimed at modulating and thereby restoring brain function, the landscape of existing interventions encompasses a very wide scope of techniques and protocols. Despite vigorous research efforts, few approaches have been assessed with rigorous, high-quality randomized controlled trials. As a growing number of exploratory interventions emerge, it is paramount to develop standardized approaches to reporting results. The successful evaluation of novel interventions depends on implementation of shared nomenclature and infrastructure. To address this gap, the Neurocritical Care Society's Curing Coma Campaign convened nine working groups and charged them with developing common data elements (CDEs). Here, we report the work of the Therapeutic Interventions Working Group., Methods: The working group reviewed existing CDEs relevant to therapeutic interventions within the National Institutes of Health National Institute of Neurological Disorders and Stroke database and reviewed the literature for assessing key areas of research in the intervention space. CDEs were then proposed, iteratively discussed and reviewed, classified, and organized in a case report form (CRF)., Results: We developed a unified CRF, including CDEs and key design elements (i.e., methodological or protocol parameters), divided into five sections: (1) patient information, (2) general study information, (3) behavioral interventions, (4) pharmacological interventions, and (5) device interventions., Conclusions: The newly created CRF enhances systematization of future work by proposing a portfolio of measures that should be collected in the development and implementation of studies assessing novel interventions intended to increase the level of consciousness or rate of recovery of consciousness in patients with disorders of consciousness., (© 2023. Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society.)
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- 2024
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149. Research considerations for prospective studies of patients with coma and disorders of consciousness.
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Tinti L, Lawson T, Molteni E, Kondziella D, Rass V, Sharshar T, Bodien YG, Giacino JT, Mayer SA, Amiri M, Muehlschlegel S, Venkatasubba Rao CP, Vespa PM, Menon DK, Citerio G, Helbok R, and McNett M
- Abstract
Disorders of consciousness are neurological conditions characterized by impaired arousal and awareness of self and environment. Behavioural responses are absent or are present but fluctuate. Disorders of consciousness are commonly encountered as a consequence of both acute and chronic brain injuries, yet reliable epidemiological estimates would require inclusive, operational definitions of the concept, as well as wider knowledge dissemination among involved professionals. Whereas several manifestations have been described, including coma, vegetative state/unresponsive wakefulness syndrome and minimally conscious state, a comprehensive neurobiological definition for disorders of consciousness is still lacking. The scientific literature is primarily observational, and studies-specific aetiologies lead to disorders of consciousness. Despite advances in these disease-related forms, there remains uncertainty about whether disorders of consciousness are a disease-agnostic unitary entity with a common mechanism, prognosis or treatment response paradigm. Our knowledge of disorders of consciousness has also been hampered by heterogeneity of study designs, variables, and outcomes, leading to results that are not comparable for evidence synthesis. The different backgrounds of professionals caring for patients with disorders of consciousness and the different goals at different stages of care could partly explain this variability. The Prospective Studies working group of the Neurocritical Care Society Curing Coma Campaign was established to create a platform for observational studies and future clinical trials on disorders of consciousness and coma across the continuum of care. In this narrative review, the author panel presents limitations of prior observational clinical research and outlines practical considerations for future investigations. A narrative review format was selected to ensure that the full breadth of study design considerations could be addressed and to facilitate a future consensus-based statement (e.g. via a modified Delphi) and series of recommendations. The panel convened weekly online meetings from October 2021 to December 2022. Research considerations addressed the nosographic status of disorders of consciousness, case ascertainment and verification, selection of dependent variables, choice of covariates and measurement and analysis of outcomes and covariates, aiming to promote more homogeneous designs and practices in future observational studies. The goal of this review is to inform a broad community of professionals with different backgrounds and clinical interests to address the methodological challenges imposed by the transition of care from acute to chronic stages and to streamline data gathering for patients with disorders of consciousness. A coordinated effort will be a key to allow reliable observational data synthesis and epidemiological estimates and ultimately inform condition-modifying clinical trials., Competing Interests: The authors report no competing interests., (© The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain.)
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- 2024
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150. Pediatric disorders of consciousness: Considerations, controversies, and caveats.
- Author
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Slomine B and Molteni E
- Subjects
- Adult, Humans, Child, Consciousness, Prognosis, Persistent Vegetative State, Consciousness Disorders diagnosis, Consciousness Disorders therapy, Brain Injuries
- Abstract
Pediatric disorders of consciousness (PedDOC) encompass conditions that may occur following very severe traumatic or other forms of acquired brain injury sustained during childhood. As in adults, PedDOC is described as a disturbance of awareness and/or responsiveness. PedDOC is a complex condition that requires specialized care, infrastructures, and technologies. PedDOC poses many challenges to healthcare providers and caregivers during recovery and throughout development. In this commentary, we intend to highlight some considerations, controversies, and caveats on the diagnosis, prognosis and treatment of PedDOC.
- Published
- 2024
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