158 results on '"Zoghi, S."'
Search Results
2. Seroprevalence of anti-Helicobacter pylori antibodies in population of Azerbaijan, Iran
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Leylabadlo, H. E., primary, Hamzehzadeh, S., additional, Sarbakhsh, P., additional, Zoghi, S., additional, and Ghotaslou, R., additional
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- 2023
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3. Exome sequencing revealed C1Q homozygous mutation in Pediatric Systemic Lupus Erythematosus
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Zoghi, S., Ziaee, V., Hirschmugl, T., Jimenez-Heredia, R., Krolo, A., Boztug, K., and Rezaei, N.
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- 2018
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4. MHC class II deficiency: Report of a novel mutation and special review
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Farrokhi, S., Shabani, M., Aryan, Z., Zoghi, S., Krolo, A., Boztug, K., and Rezaei, N.
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- 2018
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5. Novel AICDA mutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity
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Fazel, A., Kashef, S., Aleyasin, S., Harsini, S., Karamizadeh, Z., Zoghi, S., Flores, S.K., Boztug, K., and Rezaei, N.
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- 2017
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- View/download PDF
6. Systemic Inflammation and Normocytic Anemia in DOCK11 Deficiency
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Block, J., Rashkova, C., Castanon, I., Zoghi, S., Platon, J., Ardy, Rico Chandra, Fujiwara, M., Made, C.I. van der, Hoischen, A., Dupre, Loic, Boztug, Kaan, Block, J., Rashkova, C., Castanon, I., Zoghi, S., Platon, J., Ardy, Rico Chandra, Fujiwara, M., Made, C.I. van der, Hoischen, A., Dupre, Loic, and Boztug, Kaan
- Abstract
Item does not contain fulltext
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- 2023
7. Association of interleukin-1 family gene polymorphisms with juvenile idiopathic arthritis in Iranian population
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Ziaee, V., Maddah, M., Harsini, S., Rezaei, A., Sadr, M., Zoghi, S., Moradinejad, M.H., and Rezaei, N.
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- 2016
- Full Text
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8. Association of Interleukin-2, but not Interferon-Gamma, single nucleotide polymorphisms with juvenile idiopathic arthritis
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Maddah, M., Harsini, S., Rezaei, A., Sadr, M., Zoghi, S., Moradinejad, M.H., Ziaee, V., and Rezaei, N.
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- 2016
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9. Systemic Inflammation and Normocytic Anemia in DOCK11 Deficiency
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Block J, Rashkova C, Castanon I, Zoghi S, Platon J, Ardy RC, Fujiwara M, Chaves B, Schoppmeyer R, van der Made CI, Jimenez Heredia R, Harms FL, Alavi S, Alsina L, Sanchez Moreno P, Ávila Polo R, Cabrera-Pérez R, Kostel Bal S, Pfajfer L, Ransmayr B, Mautner AK, Kondo R, Tinnacher A, Caldera M, Schuster M, Domínguez Conde C, Platzer R, Salzer E, Boyer T, Brunner HG, Nooitgedagt-Frons JE, Iglesias E, Deyà-Martinez A, Camacho-Lovillo M, Menche J, Bock C, Huppa JB, Pickl WF, Distel M, Yoder JA, Traver D, Engelhardt KR, Linden T, Kager L, Hannich JT, Hoischen A, Hambleton S, Illsinger S, Da Costa L, Kutsche K, Chavoshzadeh Z, van Buul JD, Antón J, Calzada-Hernández J, Neth O, Viaud J, Nishikimi A, Dupré L, Boztug K
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- 2023
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10. Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity
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Haimel, M., Pazmandi, J., Heredia, R.J., Dmytrus, J., Bal, S.K., Zoghi, S., Daele, P. van, Briggs, T.A., Wouters, C., Bader-Meunier, B., Aeschlimann, F.A., Caorsi, R., Eleftheriou, D., Hoppenreijs, E.P., Salzer, E., Bakhtiar, S., Derfalvi, B., Saettini, F., Kusters, M.A.A., Elfeky, R., Trück, J., Rivière, J.G., Burg, M. van der, Gattorno, M., Seidel, M.G., Burns, S., Warnatz, K., Hauck, F., Brogan, P., Gilmour, K.C., Schuetz, C., Simon, A., Bock, C., Hambleton, S., Vries, E de, Robinson, P.N., Gijn, M. van, Boztug, K., Haimel, M., Pazmandi, J., Heredia, R.J., Dmytrus, J., Bal, S.K., Zoghi, S., Daele, P. van, Briggs, T.A., Wouters, C., Bader-Meunier, B., Aeschlimann, F.A., Caorsi, R., Eleftheriou, D., Hoppenreijs, E.P., Salzer, E., Bakhtiar, S., Derfalvi, B., Saettini, F., Kusters, M.A.A., Elfeky, R., Trück, J., Rivière, J.G., Burg, M. van der, Gattorno, M., Seidel, M.G., Burns, S., Warnatz, K., Hauck, F., Brogan, P., Gilmour, K.C., Schuetz, C., Simon, A., Bock, C., Hambleton, S., Vries, E de, Robinson, P.N., Gijn, M. van, and Boztug, K.
- Abstract
Contains fulltext : 248208.pdf (Publisher’s version ) (Open Access), BACKGROUND: Accurate, detailed, and standardized phenotypic descriptions are essential to support diagnostic interpretation of genetic variants and to discover new diseases. The Human Phenotype Ontology (HPO), extensively used in rare disease research, provides a rich collection of vocabulary with standardized phenotypic descriptions in a hierarchical structure. However, to date, the use of HPO has not yet been widely implemented in the field of inborn errors of immunity (IEIs), mainly due to a lack of comprehensive IEI-related terms. OBJECTIVES: We sought to systematically review available terms in HPO for the depiction of IEIs, to expand HPO, yielding more comprehensive sets of terms, and to reannotate IEIs with HPO terms to provide accurate, standardized phenotypic descriptions. METHODS: We initiated a collaboration involving expert clinicians, geneticists, researchers working on IEIs, and bioinformaticians. Multiple branches of the HPO tree were restructured and extended on the basis of expert review. Our ontology-guided machine learning coupled with a 2-tier expert review was applied to reannotate defined subgroups of IEIs. RESULTS: We revised and expanded 4 main branches of the HPO tree. Here, we reannotated 73 diseases from 4 International Union of Immunological Societies-defined IEI disease subgroups with HPO terms. We achieved a 4.7-fold increase in the number of phenotypic terms per disease. Given the new HPO annotations, we demonstrated improved ability to computationally match selected IEI cases to their known diagnosis, and improved phenotype-driven disease classification. CONCLUSIONS: Our targeted expansion and reannotation presents enhanced precision of disease annotation, will enable superior HPO-based IEI characterization, and hence benefit both IEI diagnostic and research activities.
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- 2022
11. P1408: MONOALLELIC AND BIALLELIC GERMLINE MUTATIONS AFFECTING THE TRANSCRIPTION FACTOR HELIOS CAUSE PLEIOTROPIC DEFECTS OF IMMUNITY
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Mayr, D., primary, Shahin, T., additional, Shoeb, M., additional, Kuehn, H. S., additional, Hoeger, B., additional, Giuliani, S., additional, Gawriyski, L., additional, Yüce Petronczki, Ö., additional, Hadjadj, J., additional, Köstel Bal, S., additional, Zoghi, S., additional, Haimel, M., additional, Jimenez Heredia, R., additional, Boutboul, D., additional, Triebwasser, M., additional, Rialland-Battisti, F., additional, Tangye, S., additional, Fleisher, T., additional, Rezaei, N., additional, Romberg, N., additional, Latour, S., additional, Varjosalo, M., additional, Halbritter, F., additional, Rieux-Laucat, F., additional, Castanon, I., additional, Rosenzweig, S., additional, and Boztug, K., additional
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- 2022
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12. International efforts to save healthcare personnel during COVID-19
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Mohamed, K., Rodríguez-Román, E., Rahmani, F., Zhang, H., Ivanovska, M., Makka, S.A., Joya, M., Makuku, R., Islam, M.S. (Mohammad S.), Radwan, N., Rahmah, L., Goda, R., Abarikwu, S.O., Shaw, M. (Michael), Zoghi, S., Irtsyan, S., Ling, I., Cseprekal, O., Faten, A.B., Sayar, E.H., Soloukey, C., Grancini, G., Rezaei, N, Mohamed, K., Rodríguez-Román, E., Rahmani, F., Zhang, H., Ivanovska, M., Makka, S.A., Joya, M., Makuku, R., Islam, M.S. (Mohammad S.), Radwan, N., Rahmah, L., Goda, R., Abarikwu, S.O., Shaw, M. (Michael), Zoghi, S., Irtsyan, S., Ling, I., Cseprekal, O., Faten, A.B., Sayar, E.H., Soloukey, C., Grancini, G., and Rezaei, N
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- 2020
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13. International efforts to save healthcare personnel during COVID-19
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Mohamed, K, Rodríguez-Román, E, Rahmani, F, Zhang, H, Ivanovska, M, Makka, SA, Joya, M, Makuku, R, Islam, MS, Radwan, N, Rahmah, L, Goda, R, Abarikwu, SO, Shaw, M, Zoghi, S, Irtsyan, S, Ling, I, Cseprekal, O, Faten, AB, Sayar, EH, Soloukey Tbalvandany, Sadaf, Grancini, G, Rezaei, N, Mohamed, K, Rodríguez-Román, E, Rahmani, F, Zhang, H, Ivanovska, M, Makka, SA, Joya, M, Makuku, R, Islam, MS, Radwan, N, Rahmah, L, Goda, R, Abarikwu, SO, Shaw, M, Zoghi, S, Irtsyan, S, Ling, I, Cseprekal, O, Faten, AB, Sayar, EH, Soloukey Tbalvandany, Sadaf, Grancini, G, and Rezaei, N
- Published
- 2020
14. Immunomodulation of alloreactive T-cell responses by inhibition of the CD40-mediated activation of antigenpresenting cells through blockade of protein isoprenylation: V730
- Author
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Shimabukuro-Vornhaágen, A., Zoghi, S., Theurich, S., Holtick, U., Scheid, C., and von Bergwelt-Baildon, M. S.
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- 2011
15. Whole Exome Sequencing Could Help to Distinguish Between Pediatric Systemic Lupus Erythematosus and Primary Immunodeficiency Disease
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Zoghi, S. and Nima Rezaei
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lcsh:R5-920 ,No keywords#### ,lcsh:Medicine (General) - Abstract
No Abstract
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- 2018
16. Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
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Toubiana, J., Okada, S., Hiller, J., Oleastro, M., Lagos Gomez, M., Aldave Becerra, J. C., Ouachee-Chardin, M., Fouyssac, F., Girisha, K. M., Etzioni, A., Van Montfrans, J., Camcioglu, Y., Kerns, L. A., Belohradsky, B., Blanche, S., Bousfiha, A., Rodriguez-Gallego, C., Meyts, I., Kisand, K., Reichenbach, J., Renner, E. D., Rosenzweig, S., Grimbacher, B., van de Veerdonk, F. L., Traidl-Hoffmann, C., Picard, C., Marodi, L., Morio, T., Kobayashi, M., Lilic, D., Milner, J. D., Holland, S., Casanova, J. -L., Puel A, Cypowyj S, Thumerelle C, Toulon A, Bustamante J, Tahuil N, SALHI, DALILA, Boiu S, Chopra C, Di Giovanni D, Bezrodnik L, Boutros J, Thomas C, Lacuesta G, Jannier S, Korganow AS, Paillard C, Boutboul, Bué M, Marie-Cardine A, Bayart S, Migaud M, Weiss, Karmochkine M, Garcia-Martinez JM, Stephan JL, Bensaid P, Jeannoel GP, Witte T, Baumann U, Harrer T, Navarrete C, ACOSTA HUGHES, BENJAMIN, Firinu, Pignata C, Picco P, Mendoza D, Lugo Reyes SO, Torres Lozano C, Ortega-Cisneros M, Cortina M, Mesdaghi M, Nabavi M, Español T, Martínez-Saavedra MT, Rezaei N, Zoghi S, Pac M, Barlogis V, Revon-Rivière G, Haimi-Cohen Y, Spiegel R, Miron D, Bouchaib J, Blancas-Galicia L, Toth B, Drexel B, Rohrlich PS, Lesens O, Hoernes M, Drewe E, Abinum M, Sawalle-Belohradsky J, Kindle G, Depner M, Milani L, Nikopensius T, Remm M, Talas UG, Tucker M, Willis M, Leonard S, Meuwissen H, Ferdman RM, CORBO UGULINO, WALLACE, Desai MM, Taur P, Badolato R, Soltesz B, Schnopp C, Jansson AF, Ayvaz D, Shabashova N, Chernyshova L, Bondarenko A, Moshous D, Neven B, Boubidi C, Ailal F, Giardino G, Del Giacco S, Bougnoux ME, Imai K, Okawa T, Mizoguchi Y, Ozaki Y, Takeuchi M, Hayakawa A, Lögering B, Reich K, Buhl T, Eyerich K, Schaller M, Arkwright PD, Gennery AR, Cant AJ, Warris A, Henriet S, Mekki N, Barbouche R, Ben Mustapha I, Bodemer, Polak M, Grimprel E, Burgel PR, Fischer A, Hermine O, Debré M, Kocacyk D, Dhalla F, Patel SY, Moens L, Haerynck F, Dullaers, Hoste L, Sanal O, Kilic SS, Roesler J, Lanternier F, Lortholary O, Fieschi C, Church JA, Roifman C, Yuenyongviwat A, Peterson P, Boisson-Dupuis S, Abel L, Marciano BE, Netea MG., Toubiana, J., Okada, S., Hiller, J., Oleastro, M., Lagos Gomez, M., Aldave Becerra, J. C., Ouachee-Chardin, M., Fouyssac, F., Girisha, K. M., Etzioni, A., Van Montfrans, J., Camcioglu, Y., Kerns, L. A., Belohradsky, B., Blanche, S., Bousfiha, A., Rodriguez-Gallego, C., Meyts, I., Kisand, K., Reichenbach, J., Renner, E. D., Rosenzweig, S., Grimbacher, B., van de Veerdonk, F. L., Traidl-Hoffmann, C., Picard, C., Marodi, L., Morio, T., Kobayashi, M., Lilic, D., Milner, J. D., Holland, S., Casanova, J. -L., Puel, A, Cypowyj, S, Thumerelle, C, Toulon, A, Bustamante, J, Tahuil, N, Salhi, Dalila, Boiu, S, Chopra, C, Di Giovanni, D, Bezrodnik, L, Boutros, J, Thomas, C, Lacuesta, G, Jannier, S, Korganow, A, Paillard, C, Boutboul, Bué, M, Marie-Cardine, A, Bayart, S, Migaud, M, Weiss, Karmochkine, M, Garcia-Martinez, Jm, Stephan, Jl, Bensaid, P, Jeannoel, Gp, Witte, T, Baumann, U, Harrer, T, Navarrete, C, ACOSTA HUGHES, Benjamin, Firinu, Pignata, C, Picco, P, Mendoza, D, Lugo Reyes, So, Torres Lozano, C, Ortega-Cisneros, M, Cortina, M, Mesdaghi, M, Nabavi, M, Español, T, Martínez-Saavedra, Mt, Rezaei, N, Zoghi, S, Pac, M, Barlogis, V, Revon-Rivière, G, Haimi-Cohen, Y, Spiegel, R, Miron, D, Bouchaib, J, Blancas-Galicia, L, Toth, B, Drexel, B, Rohrlich, P, Lesens, O, Hoernes, M, Drewe, E, Abinum, M, Sawalle-Belohradsky, J, Kindle, G, Depner, M, Milani, L, Nikopensius, T, Remm, M, Talas, Ug, Tucker, M, Willis, M, Leonard, S, Meuwissen, H, Ferdman, Rm, CORBO UGULINO, Wallace, Desai, Mm, Taur, P, Badolato, R, Soltesz, B, Schnopp, C, Jansson, Af, Ayvaz, D, Shabashova, N, Chernyshova, L, Bondarenko, A, Moshous, D, Neven, B, Boubidi, C, Ailal, F, Giardino, G, Del Giacco, S, Bougnoux, Me, Imai, K, Okawa, T, Mizoguchi, Y, Ozaki, Y, Takeuchi, M, Hayakawa, A, Lögering, B, Reich, K, Buhl, T, Eyerich, K, Schaller, M, Arkwright, Pd, Gennery, Ar, Cant, Aj, Warris, A, Henriet, S, Mekki, N, Barbouche, R, Ben Mustapha, I, Bodemer, Polak, M, Grimprel, E, Burgel, Pr, Fischer, A, Hermine, O, Debré, M, Kocacyk, D, Dhalla, F, Patel, Sy, Moens, L, Haerynck, F, Dullaers, Hoste, L, Sanal, O, Kilic, S, Roesler, J, Lanternier, F, Lortholary, O, Fieschi, C, Church, Ja, Roifman, C, Yuenyongviwat, A, Peterson, P, Boisson-Dupuis, S, Abel, L, Marciano, Be, and Netea, Mg.
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Male ,0301 basic medicine ,Pediatrics ,Clinical Trials and Observations ,lnfectious Diseases and Global Health Radboud Institute for Molecular Life Sciences [Radboudumc 4] ,medicine.disease_cause ,Biochemistry ,Gastroenterology ,Cohort Studies ,STAT5 Transcription Factor ,Medicine ,Chronic mucocutaneous candidiasis ,Child ,Hematology ,biology ,Progressive multifocal leukoencephalopathy ,Candidiasis, Chronic Mucocutaneous ,Candidiasis ,Orvostudományok ,Middle Aged ,Phenotype ,STAT1 Transcription Factor ,Staphylococcus aureus ,Child, Preschool ,Female ,STAT3 Transcription Factor ,Adult ,Heterozygote ,medicine.medical_specialty ,Adolescent ,Aged ,Genetic Predisposition to Disease ,Humans ,Infant ,Young Adult ,Genetic Association Studies ,Mutation ,Immunology ,Cell Biology ,Chronic Mucocutaneous ,Klinikai orvostudományok ,Herpesviridae ,Mycobacterium tuberculosis ,03 medical and health sciences ,Internal medicine ,Journal Article ,ddc:610 ,Preschool ,Key Points AD STAT1 GOF is the most common genetic cause of inherited CMC and is not restricted to a specific age or ethnic group. STAT1 GOF underlies a variety of infectious and autoimmune features, as well as carcinomas and aneurysms associated with a poor outcome ,Type 1 diabetes ,Cytopenia ,business.industry ,medicine.disease ,biology.organism_classification ,030104 developmental biology ,business - Abstract
Contains fulltext : 172671.pdf (Publisher’s version ) (Closed access) Since their discovery in patients with autosomal dominant (AD) chronic mucocutaneous candidiasis (CMC) in 2011, heterozygous STAT1 gain-of-function (GOF) mutations have increasingly been identified worldwide. The clinical spectrum associated with them needed to be delineated. We enrolled 274 patients from 167 kindreds originating from 40 countries from 5 continents. Demographic data, clinical features, immunological parameters, treatment, and outcome were recorded. The median age of the 274 patients was 22 years (range, 1-71 years); 98% of them had CMC, with a median age at onset of 1 year (range, 0-24 years). Patients often displayed bacterial (74%) infections, mostly because of Staphylococcus aureus (36%), including the respiratory tract and the skin in 47% and 28% of patients, respectively, and viral (38%) infections, mostly because of Herpesviridae (83%) and affecting the skin in 32% of patients. Invasive fungal infections (10%), mostly caused by Candida spp. (29%), and mycobacterial disease (6%) caused by Mycobacterium tuberculosis, environmental mycobacteria, or Bacille Calmette-Guerin vaccines were less common. Many patients had autoimmune manifestations (37%), including hypothyroidism (22%), type 1 diabetes (4%), blood cytopenia (4%), and systemic lupus erythematosus (2%). Invasive infections (25%), cerebral aneurysms (6%), and cancers (6%) were the strongest predictors of poor outcome. CMC persisted in 39% of the 202 patients receiving prolonged antifungal treatment. Circulating interleukin-17A-producing T-cell count was low for most (82%) but not all of the patients tested. STAT1 GOF mutations underlie AD CMC, as well as an unexpectedly wide range of other clinical features, including not only a variety of infectious and autoimmune diseases, but also cerebral aneurysms and carcinomas that confer a poor prognosis.
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- 2016
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17. Identification of the mevalonate pathway as a potential therapeutic target for EBV-reactivation and PTLD
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Shimabukuro-Vornhagen, A., Zoghi, S., von Bergwelt-Baildon, M., Shimabukuro-Vornhagen, A., Zoghi, S., and von Bergwelt-Baildon, M.
- Published
- 2017
18. The status of FOXP3gene methylation in pediatric systemic lupus erythematosus
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Hanaei, S., Sanati, G., Zoghi, S., Gharibzadeh, S., Ziaee, V., and Rezaei, N.
- Abstract
Systemic lupus erythematosus (SLE) is an autoimmune disease caused by interaction of genetic, epigenetic, and environmental factors. One of the important epigenetic factors in SLE would be methylation of immune-related genes, such as FOXP3, which plays a role in activating the regulation and also the function of T cells. To date, the relationship between levels of serum bio-markers and the susceptibility to lupus in children has not been well-understood. In this study, the involvement of etiologic factors, such as methylation of FOXP3gene, was investigated in children with SLE.
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- 2020
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19. Association of tumour necrosis factor-alpha G/A -238 and G/A -308 single nucleotide polymorphisms with juvenile idiopathic arthritis
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Maddah, M., primary, Harsini, S., additional, Ziaee, V., additional, Moradinejad, M. H., additional, Rezaei, A., additional, Zoghi, S., additional, Sadr, M., additional, Aghighi, Y., additional, and Rezaei, N., additional
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- 2016
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20. In Vitro Effects of Sodium Benzoate on Th1/Th2 Deviation in Patients with Multiple Sclerosis
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Rezaei, N., primary, Amirghofran, Z., additional, Nikseresht, A., additional, Ashjazade, N., additional, Zoghi, S., additional, Tahvili, S., additional, and Kamali-Sarvestani, E., additional
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- 2016
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21. Interleukin 10 and transforming growth factor beta 1 gene polymorphisms in juvenile idiopathic arthritis
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Harsini, S., primary, Ziaee, V., additional, Maddah, M., additional, Rezaei, A., additional, Sadr, M., additional, Zoghi, S., additional, Moradinejad, M. H., additional, Tahghighi, F., additional, Aghighi, Y., additional, and Rezaei, N., additional
- Published
- 2016
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22. Absence of asymptomatic malaria infection in endemic area of bashagard district, hormozgan province, iran
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Habibollah Turki, Zoghi, S., Mehrizi, A. A., Zakeri, S., Raeisi, A., Khazan, H., Haghdoost, A. A., Malaria and Vector Research Group (MVRG), Institut Pasteur d'Iran, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Department of Parasitology and Mycology, School of Medicine-Shahid Beheshti University of Medical Sciences [Tehran] (SBUMS), Shahid Beheshti University-Shahid Beheshti University, School of Public Health [Teheran], University of Tehran, National Programme Manager for Malaria Control, Ministry of Health and Medical Education, School of Public Health, Kerman University of Medical Science, and This work was supported by a grant (no. 483) from the Iranian Ministry of Health and Medical Education and Pasteur Institute of Iran.
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Asymptomatic malaria ,MSP-1 19 ,parasitic diseases ,Plasmodium falciparum ,[SDV.IMM]Life Sciences [q-bio]/Immunology ,Original Article ,lcsh:RC109-216 ,Iran ,Plasmodium vivax ,MSP-119 ,lcsh:Infectious and parasitic diseases - Abstract
International audience; BACKGROUND: A successful malaria elimination program calls for enough attention to parasite carriers, especially asymptomatic malaria, as well as the diagnosis and treatment of clinical cases. Asymptomatic malaria is an infection that patients do not show any symptom; thus, these patients play critical role in the concept of an elimination program. The current investigation was conducted to evaluate the presence of these cases in Bashagard District, formerly a high malaria transmission area in Hormozgan Province, Iran. METHODS: Blood samples (n = 500) were collected from symptomless individuals residing in Bashagard to evaluate Plasmodium infection by using microscopic, serological and nested-PCR techniques. RESULTS: Regarding the microscopic and nested-PCR analysis, no asymptomatic infection was detected among studied individuals. Totally, 1% of the studied population (5 of 500) had anti PvMSP-1(19)-specific IgG antibody; however, only 0.2% (1 of 500) of the individuals was seropositive to recombinant PfMSP-1(19), using ELISA. CONCLUSION: This study showed no asymptomatic malaria infection in the studied population; hence malaria elimination is feasible and can be successfully carried out in this region.
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- 2012
23. Improving human capital through engineering and entrepreneurship
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Zoghi, S., primary and Liguori, E., additional
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- 2015
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24. Pulmonary sarcoidosis shortly after spinal tuberculosis infection: a diagnostic challenge
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Luetkens, J. A., primary, Zoghi, S., additional, Rockstroh, J. K., additional, and Naehle, C. P., additional
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- 2014
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25. Novel AICDAmutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity
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Fazel, A., Kashef, S., Aleyasin, S., Harsini, S., Karamizadeh, Z., Zoghi, S., Flores, S.K., Boztug, K., and Rezaei, N.
- Abstract
The Hyper-immunoglobulin M syndromes (HIGM) are a heterogeneous group of genetic disorders, which have been rarely reported to be associated with growth hormone deficiency (GHD).
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- 2017
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26. Statins Inhibit The Antigen-Presenting Function Of Human B Cells
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Shimabukuro-Vornhagen, A., primary, Zoghi, S., additional, Liebig, T., additional, and von Bergwelt-Baildon, M., additional
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- 2010
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27. Absence of Asymptomatic Malaria Infection in Endemic Area of Bashagard District, Hormozgan Province, Iran.
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Turki, H., Zoghi, S., Mehrizi, A. A., Zakeri, S., Raeisi, A., Khazan, H., and Haghdoost, A. A.
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- *
ASYMPTOTES , *ENDEMIC animals , *MALARIA - Abstract
Background: A successful malaria elimination program calls for enough attention to parasite carriers, especially asymptomatic malaria, as well as the diagnosis and treatment of clinical cases. Asymptomatic malaria is an infection that patients do not show any symptom; thus, these patients play critical role in the concept of an elimination program. The current investigation was conducted to evaluate the presence of these cases in Bashagard District, formerly a high malaria transmission area in Hormozgan Province, Iran. Methods: Blood samples (n=500) were collected from symptomless individuals residing in Bashagard to evaluate Plasmodium infection by using microscopic, serological and nested-PCR techniques. Results: Regarding the microscopic and nested-PCR analysis, no asymptomatic infection was detected among studied individuals. Totally, 1% of the studied population (5 of 500) had anti PvMSP-119-specific IgG antibody; however, only 0.2% (1 of 500) of the individuals was seropositive to recombinant PfMSP-119, using ELISA. Conclusion: This study showed no asymptomatic malaria infection in the studied population; hence malaria elimination is feasible and can be successfully carried out in this region. [ABSTRACT FROM AUTHOR]
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- 2012
28. Association of the single nucleotide polymorphisms of the genes encoding IL-2 and IFN-γ with febrile seizure
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Shahrokhi, A., Zare-Shahabadi, A., Poor, M. N., Sajedi, F., Soltani, S., Zoghi, S., Badv, R. S., Mahmoud Reza Ashrafi, and Rezaei, N.
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Male ,lcsh:R5-920 ,Genotype ,Etiology ,Febrile seizure ,Gene polymorphisms ,Infant ,Polymorphism, Single Nucleotide ,Seizures, Febrile ,Interferon-gamma ,Gene Frequency ,Haplotypes ,Case-Control Studies ,Child, Preschool ,Humans ,Interleukin-2 ,Female ,Genetic Predisposition to Disease ,Child ,lcsh:Medicine (General) ,IFN-γ ,Alleles - Abstract
Inflammatory elements and genetics have major roles in febrile seizures (FS) pathogenesis. Seventy patients were enrolled and compared with 139 controls. The allele and genotype frequency of the IL-2 gene at -330 and +166 positions and the IFN-γ at +874 position were determined. A significant positive association with GG genotype at position -330 in the patient group was found (P=0.003). Further, a positive association was detected in simple and complex FS groups at the same position (P=0.03, P=0.004). IL-2 GT haplotype was significantly more common in the patients compared to controls (P=0.0008). Higher frequency of GT haplotype was detected in simple FS patients in comparison to controls (P=0.0003). Contrary, IL-2 TG haplotype frequency was lower in complex FS group (P=0.005). Overrepresentation of certain alleles, genotypes and haplotypes in IL-2 gene in FS patients could predispose individuals to this disease.
29. Non-pathogenic heterozygous polymorphism in RAB27A gene in a case suspicious to griscelli syndrome, type II
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Eghbali, A., Rahmani, F., Aryan, Z., Borkhardt, A., Tanzifi, P., Zoghi, S., and Nima Rezaei
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lcsh:R5-920 ,No keywords### ,lcsh:Medicine (General)
30. Efficiency of nested-PCR in detecting asymptomatic cases toward malaria elimination program in an endemic area of Iran
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Turki, H., Raeisi, A., Malekzadeh, K., Amin Ghanbarnejad, Zoghi, S., Yeryan, M., Abedi Nejad, M., Mohseni, F., and Shekari, M.
- Subjects
Asymptomatic malaria ,Nested-PCR ,parasitic diseases ,Original Article ,Malaria elimination ,lcsh:RC109-216 ,lcsh:Infectious and parasitic diseases - Abstract
Background: The aim of this study was to detect low parasite and asymptomatic malaria infections by means of three malaria diagnostic tests, in a low transmission region of Minab district, Hormozgan Province, southern Iran. Methods:Blood samples of 200 healthy volunteers from Bagh-e-Malek area were evaluated using microscopic, rapid diagnostic tests (RDT) and nested-PCR to in-spect malaria parasite. Results:The results showed no Plasmodium parasite in subjects by means of mi-croscopy and RDT. However, 3 P. vivax positive samples (1.5%) were discovered by Nested-PCR while microscopy and RDT missed the cases. Conclusion:Microscopy as the gold standard method and RDT correctly identi-fied 98.5% of cases, and molecular analysis is sensitive and reliable, especially in the detection of "asymptomatic" infections for active case surveillance. Regarding the existence of asymptomatic malaria in endemic area of Hormozgan, Iran, nest-ed-PCR could be considered as a sensitive tool to interrupt malaria transmission in the country, beside the microscopic and RDT methods.
31. Role of Total Body PET/CT in Inflammatory Disorders.
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Zoghi S, Mingels C, Badawi RD, Spencer BA, Yarbrough TL, Nardo L, and Chaudhari AJ
- Abstract
Inflammatory disorders historically have been difficult to monitor with conventional PET imaging due to limitations including radiation exposure, lack of validated imaging biomarkers, low spatial resolution, and long acquisition durations. However, the recent development of long-axial field-of-view (LAFOV) PET/CT scanners may allow utilization of novel noninvasive biomarkers to diagnose, predict outcomes, and monitor therapeutic response of inflammatory conditions. LAFOV PET scanners can image most of the human body (if not the entire body) simultaneously in one bed position, with improved signal collection efficiency compared to conventional PET scanners. This allows for imaging with shorter acquisition durations, decreased injected radiotracer dose, prolonged uptake times, or a combination of any of these. In addition, LAFOV PET scanners enable whole-body dynamic imaging. Altogether, these intrinsically superior capabilities in assessing both local and systemic diseases, have allowed these scanners to make increasingly significant contributions to the assessment of inflammatory conditions. This review aims to further explore the role and benefits of LAFOV scanners for imaging various inflammatory conditions while addressing future developments and challenges faced by this technology., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: UC Davis has a research agreement and a sales-based revenue sharing agreement with United Imaging Healthcare, the manufacturer of the total-body PET/CT scanner. No other potential conflicts of interest relevant to this article exist including employment, royalties, stock options, or patents. The authors would like to acknowledge funding from the National Institutes of Health via grants R01 AR076088, R01 AR085314 and R01 CA206187. Lorenzo Nardo is principal investigator of a service agreement with United Imaging Healthcare. Lorenzo Nardo has been the PI of more than 1 service agreements with United Imaging Healthcare. Lorenzo Nardo is mentioned in a recurrent gift from United Imaging Healthcare that support the American Board of Radiology Alternate Pathway at UC Davis. Lorenzo Nardo is site PI of clinical trials supported by Novartis Pharmaceuticals Corporation. Lorenzo Nardo is PI of a clinical trial supported by Telix Pharmaceuticals. Lorenzo Nardo is PI of clinical trial supported by Lantheus Medical Imaging. Lorenzo Nardo is PI of a clinical trials supported by Curium Pharma Healthcare. Lorenzo Nardo is Co-I of a clinical trial supported by Lilly. Lorenzo Nardo has a SPEAKING ENGAGEMENT AGREEMENT with Lilly. Lorenzo Nardo is associate editor for Current Problems in Cancer. Lorenzo Nardo served a panel reviewer for the European Health and Digital Executive Agency. Lorenzo Nardo served a panel reviewer for the National Cancer Center Network (NCCN) – multiple panels. Lorenzo Nardo served a panel reviewer for the National Institutes for Health (NIH). Lorenzo Nardo is PI and co-PI of multiple National Institutes for Health (NIH) grants. Lorenzo Nardo served a committee member for the American Board of Radiology - multiple committees. Ramsey Badawi is an investigator with Lilly. Ramsey Badawi is an investigator with United Imaging Healthcare. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)
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- 2024
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32. Characteristics and outcome of patients requiring Decompressive Craniectomy for Traumatic Brain Injury: a retrospective analysis.
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Zoghi S, Ansari A, Tavanaei R, Lu VM, Yousefi O, Niakan A, Kouhpayeh SA, Taheri R, and Khalili H
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- Humans, Male, Female, Middle Aged, Adult, Retrospective Studies, Treatment Outcome, Aged, Glasgow Coma Scale, Young Adult, Decompressive Craniectomy methods, Brain Injuries, Traumatic surgery, Brain Injuries, Traumatic complications
- Abstract
Brain swelling after Traumatic Brain Injury (TBI) can elevate intracranial pressure, necessitating Decompressive Craniectomy (DC) as the preferred surgical intervention. This study aimed to analyze a large institutional database to identify clinical characteristics of patients requiring primary DC and their outcomes. We reviewed TBI patients admitted to our center from 2015 to 2021, utilizing a prospectively maintained registry. Data collected included demographics, injury mechanisms, admission findings, neuroimaging results, DC necessity, procedures during hospitalization, and functional outcomes at discharge and six-month follow-up. A total of 4,011 patients were analyzed, with 506 undergoing primary DC. Factors such as International Normalized Ratio, activated Partial Thromboplastin Time, subdural hematoma, midline shift, epidural hematoma, intracerebral hemorrhage, and the presence of compressed or absent basal cisterns were independently linked to the need for DC. Additionally, the requirement for DC correlated with an increased likelihood of tracheostomy. For patients requiring DC, older age, lower hemoglobin levels, higher Rotterdam scores, and the presence of compressed or absent basal cisterns were associated with unfavorable outcomes in mild to moderate TBI cases. In severe TBI patients, lower Glasgow Coma Scale scores and fixed pupils were linked to poor outcomes. This study represents one of the most comprehensive analyses of primary DC requirements and outcomes, revealing that the need for DC is associated with worse outcomes in TBI patients and identifying several independent predictors of outcomes across varying severity levels., Competing Interests: Declarations. Ethical approval: The study protocol was approved by the Institutional Board Review at our institution. Written informed consent was obtained from all participants on admission. Consent to participate: Written informed consent was obtained from all patients. Consent for publication: Written informed consent was obtained from all patients. Competing interests: The authors declare no competing interests., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2024
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33. Long-term outcome of adult traumatic atlantoaxial rotatory fixation: a case series.
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Eghbal K, Jangiaghdam H, Tayebi Khorami S, Shabani Mayani A, Seif B, and Zoghi S
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- Humans, Male, Adult, Female, Middle Aged, Treatment Outcome, Traction methods, Iran, Atlanto-Axial Joint injuries, Atlanto-Axial Joint diagnostic imaging, Joint Dislocations therapy, Joint Dislocations diagnostic imaging, Joint Dislocations surgery
- Abstract
Background: This case series presents five cases of adult atlantoaxial rotatory subluxation (AARS) following traumatic events, focusing on treatment strategies and long-term outcomes., Case Presentation: This paper includes four Iranian male patients and one Iranian female patient with ages ranging from 25 to 46 years old. Each case involved unique presentations and management approaches. Initial conservative treatments, including skull traction and orthoses, were attempted, but surgical intervention became necessary due to inadequate response. Surgical fixation significantly improved functional status and alleviated symptoms in all patients, leading to long-term relief. Radiological assessments demonstrated successful outcomes post-surgery., Conclusions: This study underscores the importance of considering both conservative and surgical options in managing adult atlantoaxial rotatory subluxation to achieve optimal outcomes., (© 2024. The Author(s).)
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- 2024
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34. Advancements in Tissue Engineering: A Review of Bioprinting Techniques, Scaffolds, and Bioinks.
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Zoghi S
- Abstract
Tissue engineering is a multidisciplinary field that uses biomaterials to restore tissue function and assist with drug development. Over the last decade, the fabrication of three-dimensional (3D) multifunctional scaffolds has become commonplace in tissue engineering and regenerative medicine. Thanks to the development of 3D bioprinting technologies, these scaffolds more accurately recapitulate in vivo conditions and provide the support structure necessary for microenvironments conducive to cell growth and function. The purpose of this review is to provide a background on the leading 3D bioprinting methods and bioink selections for tissue engineering applications, with a specific focus on the growing field of developing multifunctional bioinks and possible future applications., Competing Interests: The author declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article., (© The Author(s) 2024.)
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- 2024
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35. Beyond traditional predictors: the impact of the pulsatility index and cortical subarachnoid space diameter on endoscopic third ventriculostomy success.
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Habibzadeh A, Zoghi S, Ansari A, Khademolhosseini S, Masoudi MS, Feili A, Yousefi O, and Taheri R
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- Humans, Female, Male, Infant, Child, Preschool, Child, Treatment Outcome, Pulsatile Flow, Retrospective Studies, Tomography, X-Ray Computed, Adolescent, Follow-Up Studies, Ventriculostomy methods, Hydrocephalus surgery, Hydrocephalus diagnostic imaging, Hydrocephalus physiopathology, Third Ventricle surgery, Third Ventricle diagnostic imaging, Subarachnoid Space diagnostic imaging, Neuroendoscopy methods
- Abstract
Objective: Determining the long-term success of endoscopic third ventriculostomy (ETV) remains challenging. This study aimed to investigate the impact of clinical and radiological factors on ETV success in pediatric patients with hydrocephalus., Methods: The study included patients < 18 years old with hydrocephalus who underwent ETV between March 2014 and May 2021. Data including patient age, gender, history of previous shunt surgery, previous external ventricular drain placement, intraventricular hemorrhage history, and postoperative meningitis were extracted from medical records. Imaging features such as aqueductal stenosis, third ventricle floor bowing, displaced lamina terminalis, pulsatility index (PI), and maximum diameter of the cortical subarachnoid space (CSAS) were recorded for each patient using preoperative CT scans. Two independent neurosurgeons measured the CSAS maximum diameter and the PI. CSAS measurements were obtained on axial slices of the preoperative CT scans, whereas the PI was based on intraoperative third ventricle pulsatility. Patients were followed up for 1 year after surgery, with failure defined as the need for ventriculoperitoneal shunt (VPS) placement or death attributable to hydrocephalus., Results: Ninety-eight children with a mean age of 16.39 ± 19.07 months underwent ETV for hydrocephalus. No deaths were recorded, but over 6 months and 1 year of follow-up, 12.2% and 22.4% of patients, respectively, experienced documented ETV failure requiring VPS placement. At the 6-month follow-up, a smaller maximum diameter of the CSAS was significantly associated with ETV failure; multivariate analysis revealed that CSAS maximum diameter was a predictor of 6-month ETV failure. At the 1-year follow-up, a lower PI was significantly associated with ETV failure, and multivariate analysis confirmed the PI as a significant predictor of ETV failure within 1 year after surgery. CSAS and PI measurements were repeated to assess interrater reliability: the intraclass correlation coefficients were 0.897 and 0.669 for CSAS and PI, respectively., Conclusions: This study found that the CSAS maximum diameter and the PI are predictors of ETV failure at 6 months and 1 year, respectively. These findings highlight the importance of considering specific factors such as the CSAS and PI when assessing the likelihood of ETV success in pediatric patients with hydrocephalus. Further research and consideration of these factors may help optimize patient selection and improve outcomes for those undergoing ETV as a treatment for hydrocephalus.
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- 2024
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36. Post-discharge 6-Month Functional Recovery of Traumatic Brain Injury Survivors with Unfavorable Functional Status at Discharge: A Registry-Based Cohort Study.
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Zoghi S, Ansari A, Niakan A, Taheri R, and Khalili H
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- Humans, Male, Female, Middle Aged, Adult, Cohort Studies, Aged, Glasgow Outcome Scale, Survivors, Young Adult, Length of Stay statistics & numerical data, Brain Injuries, Traumatic therapy, Registries, Recovery of Function, Patient Discharge, Functional Status
- Abstract
Background: Traumatic brain injury (TBI) is a major cause of physical disabilities worldwide. Herein, we aimed to investigate the factors contributing to post-discharge recovery in patients who were discharged with an unfavorable outcome., Methods: We collected data on the characteristics of patients, with a focus on those who survived TBI but had an unfavorable outcome at discharge as measured by Glasgow Outcome Scale Extended (GOSE) categories 2, 3, and 4. Post-discharge recovery was defined as achieving a favorable functional status at 6 months (GOSE of 5 or more) with a minimum 2-point increase in GOSE., Results: Of 4011 TBI patients in our registry, 797 had an unfavorable discharge functional status. In severe TBI, 51% achieved recovery, while in mild to moderate TBI, 57% achieved recovery after 6 months. Older patients and those with shorter intensive care unit length of stay were more likely to experience post-discharge recovery in both mild to moderate and severe TBI groups. The presence of skull base fracture was also associated with post-discharge recovery in severe TBI patients. Lastly, we show that, after adjustment for potential confounders, GOSE at discharge is associated with post-discharge recovery in both mild to moderate and severe TBI patients., Conclusions: This study found that the majority of patients discharged with an unfavorable functional status were able to achieve a favorable outcome within 6 months. The novel post-discharge recovery in TBI patients might be a useful tool for illuminating the factors associated with a significant improvement after discharge., (Copyright © 2024. Published by Elsevier Inc.)
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- 2024
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37. Percutaneous transluminal angioplasty and stenting (PTAS) in patients with symptomatic intracranial vertebrobasilar artery stenosis (IVBS).
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Pourahmad R, Saleki K, Zoghi S, Hajibeygi R, Ghorani H, Javanbakht A, Goodarzi S, Alijanizadeh P, Trinh K, Shastri R, and Ghasemi-Rad M
- Abstract
Background: Approximately 20% of all transient ischaemic attacks (TIAs) and ischaemic strokes occur within the posterior circulation, with vertebrobasilar stenosis identified as the cause in roughly 25% of the cases. Studies have shown that about a quarter of these patients have atherosclerotic stenosis of at least 50% of the vertebrobasilar artery. Stenosis has been shown to be associated with an increased risk of 90-day recurrent vertebrobasilar stroke, particularly in the first few weeks, which is significantly higher when compared with patients with stenosis of the anterior circulation. Therefore, aggressive treatment is important for the patient's prognosis. Stenting is emerging as a promising therapeutic strategy for persistent ischaemia events that do not respond to the best medical treatment, but it is not without complications. We systematically reviewed the literature on percutaneous transluminal angioplasty and stenting (PTAS) for intracranial vertebrobasilar artery stenosis (IVBS)., Methods: PubMed, Web-of-Science and Scopus were searched upon the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines to include prospective/retrospective cohort, randomised/non-randomised clinical trials and case series studies describing PTAS for IVBS. Pooled rates of intervention-related complications and outcomes were analysed with random-effect model meta-analysis using StataMP V.18.0 software., Results: 31 studies were found eligible which included 1928 cases. 1103 basilar artery stenosis cases were reported in 27 studies 0.65 (95% CI 0.53, 0.76), I
2 : 99.72%. 648 vertebral cases were reported in 18 studies 0.60 (95% CI 0.49, 0.70), I2 : 97.49%. In four studies, the rate of vertebrobasilar stenosis cases calculated as a proportion of the total sample size was 0.10 (95% CI 0.05, 0. 15). Mean stenosis in 21 included studies was found to be 0.83 (95% CI 0.79, 0.88), I2 : 0.00%, which shows variation of baseline stenosis between studies was minimal. 51 deaths were recorded in 24 studies. Meta-analysis of mortality showed the overall rate of mortality was 0.03 (95% CI 0.02, 0.05), I2 : 44.90%. In 14 studies, symptomatic intracranial haemorrhage events were recorded at an overall rate of 0.01 (95% CI 0.00, 0.02), I2 : 0.00%. Generally, a follow-up period of at least 3 months was reported in the included studies. Furthermore, procedural stroke/TIA was evaluated in seven studies, four of which reported no events (0.03 (95% CI 0.00, 0.08), I2 : 20.38%). Mean time from initial symptoms to recanalisation was 23.98 (95% CI 18.56, 29.40), I2 =98.8%, p=0.00 days., Conclusion: In certain individuals with medically unresolved, severe, symptomatic and non-acute IVBS, elective vertebrobasilar PTAS appears to be both safe and effective. Various stent designs and angioplasty-assisted techniques should be taken into consideration based on the specific clinical and radiological traits of the lesions. Future randomised controlled trials are required to verify these results., Competing Interests: Competing interests: None declared., (© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)- Published
- 2024
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38. Assessing readability of online patient educational material on concussion and return to play.
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Roy JM, Prvulovic ST, Bhalla S, Casella C, Zoghi S, Gajjar A, and Bowers CA
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- Humans, Internet, Return to Sport, Reading, Brain Concussion prevention & control, Comprehension, Patient Education as Topic methods, Patient Education as Topic standards
- Abstract
Objective: Concussions are self-limited forms of mild traumatic brain injury (TBI). Gradual return to play (RTP) is crucial to minimizing the risk of second impact syndrome. Online patient educational materials (OPEM) are often used to guide decision-making. Previous literature has reported that grade-level readability of OPEM is higher than recommended by the American Medical Association and the National Institutes of Health. The authors evaluated the readability of OPEM on concussion and RTP., Methods: An online search engine was used to identify websites providing OPEM on concussion and RTP. Text specific to concussion and RTP was extracted from each website and readability was assessed using the following six standardized indices: Flesch Reading Ease (FRE), Flesch-Kincaid Grade Level, Gunning Fog Index, Coleman-Liau Index, Simple Measure of Gobbledygook Index, and Automated Readability Index. One-way ANOVA and Tukey's post hoc test were used to compare readability across sources of information., Results: There were 59 concussion and RTP articles, and readability levels exceeded the recommended 6th grade level, irrespective of the source of information. Academic institutions published OPEM at simpler readability levels (higher FRE scores). Private organizations published OPEM at more complex (higher) grade-level readability levels in comparison with academic and nonprofit institutions (p < 0.05)., Conclusions: The readability of OPEM on RTP after concussions exceeds the literacy of the average American. There is a critical need to modify the concussion and RTP OPEM to improve comprehension by a broad audience.
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- 2024
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39. Early hypocoagulable state in traumatic brain injury patients: incidence, predisposing factors, and outcomes in a retrospective cohort study.
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Zoghi S, Ansari A, Azad TD, Niakan A, Kouhpayeh SA, Taheri R, and Khalili H
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- Humans, Female, Male, Adult, Middle Aged, Retrospective Studies, Incidence, Aged, Risk Factors, Young Adult, Cohort Studies, Partial Thromboplastin Time, Brain Injuries, Traumatic complications, Blood Coagulation Disorders epidemiology, Blood Coagulation Disorders etiology
- Abstract
Coagulopathy development in traumatic brain injury (TBI) is among the significant complications that can negatively affect the clinical course and outcome of TBI patients. Timely identification of this complication is of utmost importance in the acute clinical setting. We reviewed TBI patients admitted to our trauma center from 2015 to 2021. Demographic data, mechanism of injury, findings on admission, imaging studies, procedures during hospitalization, and functional outcomes were gathered. INR with a cutoff of 1.3, platelet count less than 100 × 10⁹/L, or partial thromboplastin time greater than 40s were utilized as the markers of coagulopathy. A total of 4002 patients were included. Coagulopathy occurred in 38.1% of the patients. Age of the patients (Odds Ratio (OR) = 0.993, 95% Confidence Interval (CI) = 0.986-0.999, p = 0.028), systolic blood pressure (OR = 0.993, 95% CI = 0.989-0.998, p = 0.005), fibrinogen level (OR = 0.998, 95% CI = 0.996-0.999, p < 0.001), and hemoglobin level (OR = 0.886, 95% CI = 0.839-0.936, p < 0.001) were independently associated with coagulopathy. Furthermore, coagulopathy was independently associated with higher mortality rates and longer ICU stays. Coagulopathy had the most substantial effect on mortality of TBI patients (OR = 2.6, 95% CI = 2.1-3.3, p < 0.001), compared to other admission clinical characteristics independently associated with mortality such as fixed pupillary light reflex (OR = 1.8, 95% CI = 1.5-2.4, p < 0.001), GCS (OR = 0.91, 95% CI = 0.88-0.94, p < 0.001), and hemoglobin level (OR = 0.93, 95% CI = 0.88-0.98, p = 0.004). Early coagulopathy in TBI patients can lead to higher mortality rates. Future studies are needed to prove that early detection and correction of coagulopathy and modifiable risk factors may help improve outcomes of TBI patients., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2024
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40. Precision and Speed at Your Fingertips: An Automated Intracranial Hematoma Volume Calculation.
- Author
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Khademolhosseini S, Habibzadeh A, Zoghi S, Taheri R, Niakan A, and Khalili H
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- Humans, Intracranial Hemorrhages diagnostic imaging, Female, Male, Middle Aged, Aged, Hematoma, Epidural, Cranial diagnostic imaging, Algorithms, Tomography, X-Ray Computed methods
- Abstract
Background: Intracranial hemorrhage (ICH) is a severe condition that requires rapid diagnosis and treatment. Automated methods for calculating ICH volumes can reduce human error and improve clinical decisioPlease provide professional degrees (e.g., PhD, MD) for the corresponding author.n-making. A novel automated method has been developed that is comparable to the ABC/2 method in terms of speed and accuracy while providing more accurate volumetric data., Methods: We developed a novel automated algorithm for calculating intracranial blood volume from computed tomography (CT) scans. The algorithm consists of a Python script that processes Digital Imaging and Communications in Medicine images and determines the blood volume and ratio. The algorithm was validated against manual calculations performed by neurosurgeons., Results: Our novel automated algorithm for calculating intracranial blood volume from CT scans demonstrated excellent agreement with the ABC/2 method, with a median overall difference of just 1.46 mL. The algorithm was also validated in patient groups with ICH, epidural hematoma (EDH), and SDH, with agreement coefficients of 0.992, 0.983, and 0.997, respectively., Conclusions: The study introduces a novel automated algorithm for calculating the volumes of various ICHs (EDH, and SDH) within CT scans. The algorithm showed excellent agreement with manual calculations and outperformed the commonly used ABC/2 method, which tends to overestimate ICH volume. The automated algorithm offers a more accurate, efficient, and time-saving approach to quantifying ICH, EDH, and SDH volumes, making it a valuable tool for clinical evaluation and decision-making., (Copyright © 2024 Elsevier Inc. All rights reserved.)
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- 2024
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41. Elevated skull fractures: an institutional experience and individual participant data meta-analysis.
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Zoghi S, Habibzadeh A, Ansari A, Still MEH, Lu VM, Tabesh Z, Masoudi MS, and Taheri R
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- Female, Humans, Male, Young Adult, Retrospective Studies, Skull Fractures surgery
- Abstract
Elevated skull fracture (ESF) is a rare but potentially life-threatening type of skull fracture. The literature on this topic is relatively sparse. Herein, we conducted a meta-analysis of all the patients reported in the literature with ESFs with respect to their clinical management to better inform practice. On 20th of January 2023, we conducted a systematic search of literature to find all published cases of ESF. We also conducted a retrospective review of ESF cases from our institution. The data collection and analysis were conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. After screening, 28 studies met the inclusion criteria. A total of 104 individual patients were included in the meta-analysis, with a median age of 24 years and 85.7% of whom were males. 11 patients (11.2%) had an unfavorable outcome while 37 (35.2%) had one or more complications. We found that GCS on admission is an independent predictor of poor outcome in ESF (odds ratio (95% confidence interval) = 1.605 (1.110-2.315), p value = 0.012). Regarding complications, dural injury (odds ratio (95% confidence interval) = 66.667 (7.407-500.00), p value < 0.001) and multiple bone involvement (odds ratio (95% confidence interval) = 6.849 (2.127-22.222), p value = 0.001) were independent predictors of complication. ESFs represent a rare yet consequential form of cranial injury, carrying potentially life-threatening implications if not promptly addressed. In this study, we present the meta-analysis of outcomes and complications within this patient cohort, offering a comprehensive synthesis of existing literature on this pathology. However, further investigation is imperative to provide higher-quality evidence and address lingering uncertainties in the classification and management of ESFs., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2024
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42. Surgical outcomes of myelomeningocele repair: A 20-year experience from a single center in a middle-income country.
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Zoghi S, Feili M, Mosayebi MA, Ansari A, Feili A, Masoudi MS, and Taheri R
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- Child, Humans, Infant, Newborn, Retrospective Studies, Postoperative Complications epidemiology, Treatment Outcome, Meningomyelocele surgery, Meningomyelocele complications, Hydrocephalus surgery
- Abstract
Background and Purpose: Spina bifida is the second major cause of congenital disorders and the most common central nervous system congenital malformation compatible with life primarily. Herein, we describe the short-term outcome of post-natal Myelomeningocele (MMC) surgical management and predictors of its postoperative complications and mortality., Methods: This retrospective chart review studies the children who underwent post-natal surgical management for MMC in Namazi hospital, a tertiary referral center, in southern Iran from May 2001 to September 2020., Results: 248 patients were included in this study. The mean age at the operation was 8.47 ± 8.69 days. The most common site of involvement of MMC was Lumbosacral (86%, n = 204). At the evaluation conducted prior to the operation, cerebrospinal fluid leak was observed in 7% (n=16) of the patients. Postoperatively, 5.7% of the patients expired in the 30-day follow-up after the operation (n = 14), while 24% needed readmission (n = 47). The most common complications leading to readmission were wound dehiscence (n = 10, 42%) and wound purulence (n = 6, 25%). Only the site of the lesion (p-value = 0.035) was associated with postoperative complication. After controlling for potential confounders, the site of the lesion (adjusted odds ratio = 0.146, 95% confidence interval = 0.035-0.610, p-value = 0.008) and age at surgery (adjusted odds ratio = 1.048, 95% confidence interval = 1.002-1.096, p-value = 0.041) were significantly associated with mortality CONCLUSIONS: The age of the patients at the surgery and the site of the lesion are the two factors that were associated with mortality. However, further investigations into preoperative interventions and risk factors to mitigate the risk of complications and mortality are highly encouraged., Competing Interests: Declaration of Competing Interest The authors have no relevant financial or non-financial interests to disclose., (Copyright © 2024 Elsevier B.V. All rights reserved.)
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- 2024
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43. 2- to 20-year myelomeningocele follow-up outcomes from a referral center in Southern Iran: the Shiraz experience.
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Zoghi S, Mosayebi MA, Feili M, Eskandari H, Jalalinezhad H, Masoudi MS, and Taheri R
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- Child, Humans, Female, Pregnancy, Infant, Newborn, Follow-Up Studies, Iran epidemiology, Referral and Consultation, Retrospective Studies, Meningomyelocele surgery
- Abstract
Background: The current convention for treatment of children with myelomeningocele (MMC) is timely surgical intervention combined with long-term follow-up by a multidisciplinary specialized team. This study aims to investigate the outcomes of MMC patients treated at Namazi Hospital., Methods: All children presenting to Namazi Hospital with myelomeningocele between May 2001 and August 2020 were eligible for this study. For those with a documented telephone number, follow-up phone surveys with the patient's caregivers, on top of the review of the medical documents were carried out to assess mortality, morbidities, and the functional outcome of the care provided to them., Results: A total of 125 patients were studied (62 females). All of the patients were followed up for a mean duration of 6.28 years (range 1-23 years). The majority were located in the lumbosacral area. All of the patients underwent postnatal surgical intervention for MMC in Namazi Hospital. Mean age at surgery was 9.51 days. There were statistically significant differences between urinary and bowel incontinence and presence of scoliosis, MMT grading of the lower limbs, school attendance, number of readmissions, and requirement of laminectomy at the initial surgical intervention., Conclusions: This study is the first to characterize the long-term outcomes of MMC patients in Iran. This study illustrates that there is a great need for improved access to and coordination of care in antenatal, perioperative, and long-term stages to improve morbidity and mortality., (© 2024. The Author(s).)
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- 2024
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44. Effect of low fibrinogen level on in-hospital mortality and 6-month functional outcome of TBI patients, a single center experience.
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Yousefi O, Farrokhi A, Taheri R, Ghasemi H, Zoghi S, Eslami A, Niakan A, and Khalili H
- Subjects
- Humans, Male, Female, Young Adult, Adult, Middle Aged, Hospital Mortality, Glasgow Coma Scale, Prognosis, Fibrinogen, Afibrinogenemia complications, Brain Injuries, Traumatic complications
- Abstract
In patients affected by traumatic brain injury (TBI), hypofibrinogenemia within the initial hours of trauma can be expected due to vascular and inflammatory changes. In this study, we aimed to evaluate the effect of hypofibrinogenemia on the in-hospital mortality and 6-month functional outcomes of TBI patients, admitted to Rajaee Hospital, a referral trauma center in Shiraz, Iran. This study included all TBI patients admitted to our center who had no prior history of coagulopathy or any systemic disease, were alive on arrival, and had not received any blood product before admission. On admission, hospitalization, imaging, and 6-month follow-up information of included patients were extracted from the TBI registry database. The baseline characteristics of patients with fibrinogen levels of less than 150 mg/dL were compared with the cases with higher levels. To assess the effect of low fibrinogen levels on in-hospital mortality, a uni- and multivariate was conducted between those who died in hospital and survivors. Based on the 6-month GOSE score of patients, those with GOSE < 4 (unfavorable outcome) were compared with those with a favorable outcome. A total of 3049 patients (84.3% male, 15.7% female), with a mean age of 39.25 ± 18.87, met the eligibility criteria of this study. 494 patients had fibrinogen levels < 150 mg/dl, who were mostly younger and had lower average GCS scores in comparison to cases with higher fibrinogen levels. By comparison of the patients who died during hospitalization and survivors, it was shown that fibrinogen < 150 mg/dl is among the prognostic factors for in-hospital mortality (OR:1.75, CI: 1.32:2.34, P-value < 0.001), while the comparison between patients with the favorable and unfavorable functional outcome at 6-month follow-up, was not in favor of prognostic effect of low fibrinogen level (OR: 0.80, CI: 0.58: 1.11, P-value: 0.19). Hypofibrinogenemia is associated with in-hospital mortality of TBI patients, along with known factors such as higher age and lower initial GCS score. However, it is not among the prognostic factors of midterm functional outcome., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
- Published
- 2024
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45. Development of a Novel Neurological Score Combining GCS and FOUR Scales for Assessment of Neurosurgical Patients with Traumatic Brain Injury: GCS-FOUR Scale.
- Author
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Ansari A, Zoghi S, Khoshbooei A, Mosayebi MA, Feili M, Yousefi O, Niakan A, Kouhpayeh SA, Taheri R, and Khalili H
- Subjects
- Humans, Male, Adult, Female, Glasgow Coma Scale, Retrospective Studies, Hospitalization, Persistent Vegetative State, Brain Injuries, Traumatic diagnosis, Brain Injuries, Traumatic surgery
- Abstract
Background: Consciousness assessment is crucial for patients with traumatic brain injury. In this study, we developed a novel scoring system combining the Glasgow coma scale (GCS) and the full outline of unresponsiveness (FOUR) and evaluated its association with the intensive care unit (ICU) length of stay, mortality, and functional outcome., Methods: We retrospectively analyzed the data from patients with traumatic brain injury admitted to the neurosurgical ICU of our institution during a 2-year period. The eye and motor components of the GCS and the brainstem reflex component of the FOUR were used to compute the GCS-FOUR. We performed statistical analysis to demonstrate the association between the GCS, FOUR, and GCS-FOUR and the ICU length of stay, mortality, the development of a persistent vegetative state, and desirable recovery., Results: A total of 140 patients were included. The mean age was 30.6 years, and 89.3% were male. All 3 scores were associated with the ICU length of stay, mortality, a persistent vegetative state, and good recovery. In terms of predicting mortality, the GCS score exhibited a slight superiority compared with the other indexes, and the GCS-FOUR score showed a slight superiority over the other indexes in predicting for good recovery., Conclusions: The GCS-FOUR is a novel scoring system comparable to the GCS and FOUR regarding its association with functional status after injury, ICU length of stay, and mortality. The GCS-FOUR score provides greater neurological detail than the GCS due to the inclusion of brainstem reflexes, in addition to using the experience of healthcare providers with the GCS score compared with the FOUR in most settings., (Copyright © 2023 Elsevier Inc. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF
46. The Gut Microbiota and Major Depressive Disorder: Current Understanding and Novel Therapeutic Strategies.
- Author
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Bahmani M, Mehrtabar S, Jafarizadeh A, Zoghi S, Heravi FS, Abbasi A, Sanaie S, Rahnemayan S, and Leylabadlo HE
- Subjects
- Humans, Animals, Synbiotics administration & dosage, Gastrointestinal Microbiome, Depressive Disorder, Major microbiology, Depressive Disorder, Major therapy, Probiotics therapeutic use, Prebiotics administration & dosage, Fecal Microbiota Transplantation
- Abstract
Major depressive disorder (MDD) is a common neuropsychiatric challenge that primarily targets young females. MDD as a global disorder has a multifactorial etiology related to the environment and genetic background. A balanced gut microbiota is one of the most important environmental factors involved in human physiological health. The interaction of gut microbiota components and metabolic products with the hypothalamic-pituitary-adrenal system and immune mediators can reverse depression phenotypes in vulnerable individuals. Therefore, abnormalities in the quantitative and qualitative structure of the gut microbiota may lead to the progression of MDD. In this review, we have presented an overview of the bidirectional relationship between gut microbiota and MDD, and the effect of pre-treatments and microbiomebased approaches, such as probiotics, prebiotics, synbiotics, fecal microbiota transplantation, and a new generation of microbial alternatives, on the improvement of unstable clinical conditions caused by MDD., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)
- Published
- 2024
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47. Novel CARMIL2 (RLTPR) Mutation Presenting with Hyper-IgE and Eosinophilia: A Case Report.
- Author
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Zamani R, Zoghi S, Shahkarami S, Seyedpour S, Jimenez Heredia R, Boztug K, and Rezaei N
- Subjects
- Humans, Male, Adult, Immunoglobulin E blood, Mutation, Genetic Predisposition to Disease, Phenotype, Pedigree, Microfilament Proteins, Eosinophilia genetics, Eosinophilia diagnosis
- Abstract
Background: Inborn errors of immunity are a growing group of disorders with a wide spectrum of genotypic and phenotypic profiles. CARMIL2 (previously named RLTPR) deficiency is a recently described cause of immune dysregulation, mainly presenting with allergy, mucocutaneous infections, and inflammatory bowel disease. CARMIL2 deficiency is categorized under diseases of immune dysregulation with susceptibility to lymphoproliferative conditions., Case Presentation: Here we describe a 29-years-old male from a consanguineous family, with food and sting allergy, allergic rhinitis, facial molluscum contagiosum (viral infection of the skin in the form of umbilicated papules), eosinophilia and highly elevated serum IgE level. Whole exome sequencing revealed numerous homozygous variants, including a CARMIL2 nonsense mutation, a gene regulating actin polymerization, and promoting cell protrusion formation., Conclusion: The selective role of CARMIL2 in T cell activation and maturation through cytoskeletal organization is proposed to be the cause of immune dysregulation in individuals with CARMIL2 deficiency. CARMIL2 has an important role in immune pathways regulation, through cell maturation and differentiation, giving rise to a balance between Th1, Th2, and Th17 immune response. This case can improve the understanding of the different impacts of CARMIL2 mutations on immune pathways and further guide the diagnosis of patients with similar phenotypes., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)
- Published
- 2024
- Full Text
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48. The gut microbiota and celiac disease: Pathophysiology, current perspective and new therapeutic approaches.
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Zoghi S, Abbasi A, Heravi FS, Somi MH, Nikniaz Z, Moaddab SY, and Ebrahimzadeh Leylabadlo H
- Subjects
- Humans, Quality of Life, Intestines, Glutens, Dysbiosis, Celiac Disease therapy, Celiac Disease genetics, Gastrointestinal Microbiome, Probiotics therapeutic use
- Abstract
Celiac disease (CD) as a chronic gluten-sensitive intestinal condition, mainly affects genetically susceptible hosts. The primary determinants of CD have been identified as environmental and genetic variables. The development of CD is significantly influenced by environmental factors, including the gut microbiome. Therefore, gut microbiome re-programming-based therapies using probiotics, prebiotics, postbiotics, gluten-free diet, and fecal microbiota transplantation have shown promising results in the modification of the gut microbiome. Due to the importance and paucity of information regarding the CD pathophysiology, in this review, we have covered the association between CD development and gut microbiota, the effects of infectious agents, particularly the recent Covid-19 infection in CD patients, and the efficacy of potential therapeutic approaches in the CD have been discussed. Hence, scientific literature indicates that the diverse biological functions of the gut microbiota against immunomodulatory responses have made microbiome-based therapy an alternative therapeutic paradigm to ameliorate the symptoms of CD and quality of life. However, the exact potential of microbiota-based techniques that aims to quantitatively and qualitatively alter the gut microbiota to be used in the treatment and ameliorate the symptoms of CD will be determined with further research in the future.
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- 2024
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49. A Novel Skin Incision for Posterior Fossa Midline and Paramedian Lesions: A Technical Note and Case Series.
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Masoudi MS, Zoghi S, Taheri R, Habibzadeh A, and Ansari A
- Abstract
Approaching posterior fossa pathologies is fairly challenging. Poor exposure, cerebrospinal fluid (CSF) leak following surgery, post-operative suboccipital and neck pain, as well as wound healing are all common complications following traditional suboccipital midline incision. Herein, we present a novel incision for approaching posterior fossa pathologies. The incision is shaped like a question mark and makes a musculofascial flap supplied by the occipital artery on top as well as a wide area for craniotomy. In our technique, the dura is also incised in a question mark-shaped manner. The new incision was used to operate on three patients who had masses in the posterior fossa. Following surgeries, none of the patients experienced any adverse events such as CSF leak, wound complications, severe suboccipital pain, and neck instability. This new incision not only facilitates approaching pathologies in the posterior fossa by providing wider exposure but also enables us to perform watertight dural closure, which reduces CSF leak. Furthermore, as the muscular incision provides a sufficient area for craniotomy, muscular retraction can be minimized to reduce post-operative pain. Moreover, unlike the midline avascular incision, the flap is well supplied by the occipital artery, which facilitates the healing procedure., Competing Interests: The authors declare no conflict of interest.
- Published
- 2024
- Full Text
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50. Outcomes of the early endoscopic-assisted suturectomy for treatment of multisuture craniosynostosis.
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Yousefi O, Taheri R, Sabahi M, Reynolds RA, Farrokhi A, Zoghi S, Jamshidi A, Hoghoughi MA, Iqbal MO, Jallo GI, and Masoudi MS
- Subjects
- Infant, Child, Humans, Retrospective Studies, Skull surgery, Cranial Sutures surgery, Endoscopy methods, Treatment Outcome, Craniosynostoses surgery, Craniosynostoses complications
- Abstract
To present the outcomes and adverse events associated with the endoscopic-assisted, minimally invasive suturectomy in patients with multisuture synostosis. This retrospective cohort study included children < 65 days of age who underwent endoscopic-assisted suturectomy (EAS) for multisuture craniosynostosis at a single tertiary referral center from 2013 to 2021. The primary outcome was calvarial expansion, and the secondary outcome was adverse events. The pre- and post-operative 3-dimensional brain computed tomography (CT) scan was used to calculate the intracranial volume and cephalic index. During a period of 2 years, 10 infants (10-64 days) diagnosed with multisuture synostosis underwent single-stage EAS of every affected suture in our center. The coronal suture was the most prevalent involved suture among our cases. The mean age and weight of the patients were 39 ± 17.5 days and 4.39 ± 0.8 kg, respectively. The surgical procedure took 42 ± 17.4 min of time and caused 46 ± 25.4 mL of bleeding on average. Ninety percent of the operations were considered successful (n = 9) regarding calvarial expansion. There were two complications, one requiring an open vault surgery and one repairing a leptomeningeal cyst. In the eight patients who did not necessitate further interventions, the mean pre-operative intracranial volume was 643.3 ± 189.4 cm
3 . The follow-up results within the average of 38.9 months after surgery showed that as age increases, the intracranial volume also increased significantly (R: 0.6, P < 0.0001), which suggests continued skull growth in patients who underwent EAS. With the low rate of intra- or post-operative complications and promising results on revising the restricted skull sutures, EAS seems both a safe and effective therapeutic modality in patients with multisuture synostosis, especially if completed in the first months after birth., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)- Published
- 2023
- Full Text
- View/download PDF
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