Zobrazeno 1 - 10
of 583
pro vyhledávání: '"Mohammad Nabavi"'
Autor:
Mohammad Hassan Bemanian, Raheleh Shokouhi Shoormasti, Saba Arshi, Mahsa Jafari, Sima Shokri, Morteza Fallahpour, Mohammad Nabavi, Fatemeh Zaremehrjardi
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 20, Iss 1, Pp 1-10 (2024)
Abstract Background The poly-sensitization to Hymenoptera venom makes it difficult to select genuine allergens for immunotherapy and increases patients’ costs. The objective of this study was to determine the culprit allergen in dual or triple-sens
Externí odkaz:
https://doaj.org/article/e0115ab9d8c0464aa787c833b5415ba4
Autor:
Javad Nazari, Faezeh Shahba, Negin Jafariaghdam, Saleh Mohebbi, Saba Arshi, Mohammad Hassan Bemanian, Morteza Fallahpour, Sima Shokri, Fatemeh Atashrazm, Saeed Amini, Maryam Roomiani, Mahnaz Jamee, Pegah Babaheidarian, Majid Khoshmirsafa, Mohammad Nabavi
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 20, Iss 1, Pp 1-10 (2024)
Abstract Background Chronic Rhinosinusitis (CRS) is a paranasal sinus inflammatory disease and is divided into two subgroups defined as CRS with nasal polyps (CRSwNP) and CRS without nasal polyps (CRSsNP). CRSwNP displays a T helper (Th)2 biased phen
Externí odkaz:
https://doaj.org/article/33c3b558be114abcbb913f0d47e06879
Autor:
Nima Taghizadeh Mortezaei, Soha Mohammadi, Hassan Abolhassani, Sima Shokri, Mohammad Nabavi, Morteza Fallahpour, Mohammad Hassan Bemanian
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Severe combined immunodeficiencies (SCIDs) are hereditary disorders characterized by impaired T and B cell function, resulting in significant immune system dysfunction. Recombination-activating gene (RAG) mutations account for a s
Externí odkaz:
https://doaj.org/article/01f8a9e4e4cd4bf7bc49be9ceac0326d
Autor:
Marzieh Tavakol, Samaneh Delavari, Fereshte Salami, Sarina Ansari, Seyed Erfan Rasouli, Zahra Chavoshzadeh, Roya Sherkat, Hamid Ahanchian, Soheila Aleyasin, Hossein Esmaeilzadeh, Nasrin Moazzen, Alireza Shafiei, Farhad Abolnezhadian, Sara Iranparast, Sareh sadat Ebrahimi, Tannaz Moeini Shad, Salar Pashangzadeh, Farzad Nazari, Arezou Rezaei, Ali Saeedi-Boroujeni, Mohammad Nabavi, Saba Arshi, Morteza Fallahpour, Mohammad hassan Bemanian, Samin Sharafian, Sima Shokri, Sarvin Eshaghi, Shiva Nazari, Bibi Shahin Shamsian, Mehrdad Dargahi Mal-Amir, Roya Khazaei, Pooya Ashkevari, Armin Khavandegar, Sabahat Haghi, Marzie Esmaeili, Hassan Abolhassani, Nima Rezaei
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 18, Iss 1, Pp 1-9 (2022)
Abstract Genetic defects in the development, maturation, and/or function of the immune cells can lead to Inborn errors of immunity (IEI) which may predispose patients to malignancies. The overall risk for cancer in children with IEI ranges from 4 to
Externí odkaz:
https://doaj.org/article/78a7292b5c5c487085e67cfee390ff5b
Autor:
Sima Bahrami, Saba Arshi, Mohammad Nabavi, Mohammad Hassan Bemanian, Morteza Fallahpour, Afshin Rezaeifar, Sima Shokri
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-5 (2022)
Abstract Background Progressive multifocal leukoencephalopathy is a rare demyelinating disease that is often secondary to lytic destruction of oligodendrocytes and, to a lesser extent, to astrocytes’ response to human neurotrophic John Cunningham p
Externí odkaz:
https://doaj.org/article/ed25908178ae44c1b40103468745c43f
Autor:
Seyedeh Zalfa Modarresi, Shagayegh Tajik, Mohsen Badalzadeh, Mohammad Reza Fazlollahi, Massoud Houshmand, Marzieh Maddah, Zahra Alizadeh, Mohammad Nabavi, Nasrin Bazargan, Masoud Movahedi, Zahra Pourpak
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 22, Iss 1 (2023)
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder more common in autosomal recessive (AR) than X-linked in Iran. This study aimed to assess whether having a child with AR-CGD would increase the likelihood of the next chi
Externí odkaz:
https://doaj.org/article/7c8d3c246de348d28d1c16450ffc0417
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:
Mohammad Nabavi, Faezeh Mohammadi, Saba Arshi, Mohammad Hasan Bemanian, Morteza Fallahpour, Fatemeh Atashrazm, Sima Shokri
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 21, Iss 5 (2022)
Coronavirus disease 2019 (COVID-19) affects millions of people worldwide. Clinical manifestations range from asymptomatic to severe viral pneumonia. CVID patients with COVID-19 infection are not adequately studied. In some studies, CVID patients had
Externí odkaz:
https://doaj.org/article/ee0b0bc2aae84e4c9c805d73939d97f2
Autor:
Hamideh Nodehi, Mohammad Faranoush, Saba Arshi, Mohammad Nabavi, Mohammad Hasan Bemanian, Sima Shokri, Mohammad Reza Saghafi, Mohammad-Sadegh Fallah, Morteza Fallahpour
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 21, Iss 4 (2022)
Type 2 Griscelli syndrome (Type2 GS) is a primary inborn error of the immune system, classified in the immune dysregulation group.1,2 There are three different types of the disease, with different genetic causes responsible for the autosomal recessiv
Externí odkaz:
https://doaj.org/article/103cbbc2827f437c8d0b6260486efb66
Autor:
Mohammad Hasan Bemanian, Sima Bahrami, Saba Arshi, Afshin Rezaeifar, Mohammad Nabavi, Morteza Fallahpour, Sima Shokri
Publikováno v:
Iranian Journal of Immunology, Vol 18, Iss 2, Pp 158-162 (2021)
Immunoglobulin G4-Related Disease (IgG4-RD) is a systemic fibro-inflammatory disease that has been proposed as a separate entity since thebeginning of this century. The disease is often manifested by increasedserum IgG4 levels and certain histopathol
Externí odkaz:
https://doaj.org/article/fdc46ac8f3ae4f9fb59dc95c78ffe888