Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ahmad Vosughi Motlagh"'
Autor:
Niusha Sharifinejad, Gholamreza Azizi, Zahra Chavoshzadeh, Seyed Alireza Mahdaviani, Mahnaz Seifi Alan, Marzieh Tavakol, Homa Sadri, Mohammad Nabavi, Sareh Sadat Ebrahimi, Afshin Shirkani, Ahmad Vosughi Motlagh, Molood Safarirad, Fatemeh Aghamahdi, Farzad Nazari, Samaneh Delavari, Mahnaz Jamee, Farimah Fayyaz, Parham Samimisedeh, Rahman Matani, Marzie Esmaeili, Reza Yazdani, Nima Rezaei, Hassan Abolhassani
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundCombined immune deficiencies (CIDs) with associated or syndromic features are a highly heterogeneous subgroup of inherited immune disorders. These patients represent specific clinical complications with an increased risk of autoimmune condi
Externí odkaz:
https://doaj.org/article/47ea165aa51f44318ee6c5933141ee90
Autor:
Niusha Sharifinejad, Gholamreza Azizi, Seyed Erfan Rasouli, Zahra Chavoshzadeh, Seyed Alireza Mahdaviani, Marzieh Tavakol, Homa Sadri, Mohammad Nabavi, Sareh Sadat Ebrahimi, Afshin Shirkani, Ahmad Vosughi Motlagh, Tooba Momen, Samin Sharafian, Mehrnaz Mesdaghi, Narges Eslami, Samaneh Delavari, Sasan Bahrami, Reza Yazdani, Nima Rezaei, Hassan Abolhassani
Publikováno v:
Biology, Vol 12, Iss 5, p 644 (2023)
Cutaneous manifestations are one of the most common presentations among patients with inborn errors of immunity (IEI). These skin manifestations are often among the first presenting features in the majority of patients preceding the IEI diagnosis. We
Externí odkaz:
https://doaj.org/article/183e434dfed5430a98ef3a3d2eb67f4e
Autor:
Gholamreza Azizi, Mina Fattah Hesari, Niusha Sharifinejad, Farimah Fayyaz, Zahra Chavoshzadeh, Seyed Alireza Mahdaviani, Mahnaz Seifi Alan, Mahnaz Jamee, Marzieh Tavakol, Homa Sadri, Ehsan Shahrestanaki, Mohammad Nabavi, Sareh Sadat Ebrahimi, Afshin Shirkani, Ahmad Vosughi Motlagh, Samaneh Delavari, Seyed Erfan Rasouli, Marzie Esmaeili, Fereshte Salami, Reza Yazdani, Nima Rezaei, Hassan Abolhassani
Publikováno v:
Journal of Clinical Immunology. 43:819-834
Purpose Primary B cell defects manifesting as predominantly antibody deficiencies result from variable inborn errors of the B cell lineage and their development, including impairments in early bone marrow development, class switch recombination (CSR)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a01b9c5d6d399767037aa559a5a74de
https://doi.org/10.1007/s10875-023-01442-6
https://doi.org/10.1007/s10875-023-01442-6
Autor:
Farzad Nazari, Ali Abbaszadeh Ganji, Hassan Abolhassani, Reza Yazdani, Ahmad Vosughi Motlagh, Molood Safarirad
Publikováno v:
Allergologia et Immunopathologia. 49:63-66
Background: The coronavirus disease 2019 (COVID-19) pandemic has affected millions of people around the world. This zoonotic-enveloped virus is primarily transmitted through inhalation. Infected people are commonly asymptomatic or manifest mild sympt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e32c1ab28bf21d0ff80a16f8001d313
https://doi.org/10.15586/aei.v49i6.92
https://doi.org/10.15586/aei.v49i6.92
Autor:
Reza Yazdani, Molood Safarirad, Saba Fekrvand, Ali Abbaszadeh Ganji, Hassan Abolhassani, Ahmad Vosughi Motlagh, Asghar Aghamohammadi
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 21:2099-2103
Kabuki syndrome is a rare congenital anomaly/mental retardation syndrome characterized by intellectual disability, developmental delay, short stature, facial dysmorphic features including ectropion of the lateral third of the lower eyelids and long p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::825c3e147857416ddd0a0b0d58ad8a62
https://doi.org/10.2174/1871530321666210114153920
https://doi.org/10.2174/1871530321666210114153920
Publikováno v:
Journal of North Khorasan University of Medical Sciences. 13:86-89
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b94394a3f1226a659780be52cca6ba1
https://doi.org/10.52547/nkums.13.2.86
https://doi.org/10.52547/nkums.13.2.86
Publikováno v:
Immunology and Genetics Journal.
Objectives: X-linked Agammaglobulinemia (XLA) is a primary immunodeficiency disease, characterized by severe hypogammaglobulinemia and the low numbers of peripheral B cells. Neutropenia is a rare complication among the XLA patients, which may lead to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39e3c553eb0324dcbb88af30ecb705f2
https://doi.org/10.18502/igj.v3i4.7459
https://doi.org/10.18502/igj.v3i4.7459
Autor:
Molood, Safarirad, Ali Abbaszadeh, Ganji, Farzad, Nazari, Reza, Yazdani, Hassan, Abolhassani, Ahmad Vosughi, Motlagh
Publikováno v:
Allergologia et immunopathologia. 49(6)
The coronavirus disease 2019 (COVID-19) pandemic has affected millions of people around the world. This zoonotic-enveloped virus is primarily transmitted through inhalation. Infected people are commonly asymptomatic or manifest mild symptoms, includi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ae373f6d4b2db98b7ee22d0044cb6ea6
https://pubmed.ncbi.nlm.nih.gov/34761659
https://pubmed.ncbi.nlm.nih.gov/34761659
Autor:
Hans D. Ochs, Reza Yazdani, Zahra Chavoshzadeh, Hassan Abolhassani, Marzieh Tavakol, Martin F. Lavin, Sepideh Darougar, Alireza Shafiei, Ahmad Vosughi Motlagh
Combined immune deficiencies (CIDs) are a heterogeneous group of inherited immune disorders characterized by impaired development, function, or both of T lymphocytes, with variable B cell defects. Among CIDs, a group of disorders is associated with s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6a2bbe1da2dbf74830617cedf8c9fef
https://doi.org/10.1016/b978-0-12-821028-4.00008-7
https://doi.org/10.1016/b978-0-12-821028-4.00008-7
Autor:
Mohammad Hossein Eslamian, Marzieh Tavakol, Alireza Shafiei, Seyed Alireza Mahdaviani, Nasrin Moazzen, Hossein Esmaeilzadeh, Ahmad Vosughi Motlagh, Narges Eslami, Mahnaz Sadeghi Shabestari, Nazanin Hosseini, Akefeh Ahmadiafshar, Hamid Ahanchian, Morteza Fallahpour, Zahra Chavoshzadeh, Mohammad Nabavi, Babak Shahhosseini, Hassan Abolhassani, Nasrin Khakbazanfard, Farzad Nazari, Mazdak Fallahi, Asghar Aghamohammadi, Taher Cheraghi, Arash Kalantari, Reza Yazdani, Sima Shokri, Mohammad Hassan Bemanian, Marzieh Heidarzadeh Arani, Mojgan Safari, Maryam Khoshkhui, Saba Arshi, Seyed Hesamedin Nabavizadeh, Negar Mortazavi, Sahar Samimi, Nima Rezaei, Aida Askarisarvestani, Afshin Shirkani, Pooria Nakhaei, Rasol Molatefi, Soheila Aleyasin
Publikováno v:
Clinical Immunology. 230:108826
Background Intravenous immunoglobulins (IVIg) are the major treatment in inborn errors of immunity (IEI) disorders; However, IVIg infusions show some adverse effects. We aimed to assess the adverse reactions of IVIg infusions. Methods Data of IVIg in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e58996e7855801300edee571d329880f
https://doi.org/10.1016/j.clim.2021.108826
https://doi.org/10.1016/j.clim.2021.108826