Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Mohammad Hassan Bemanian"'
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:
Mohammad Nabavi, Afshin Rezaeifar, Morteza Fallahpour, Saba Arshi, Mohammad Hassan Bemanian, Sima Shokri, Fatemeh Atashrazm, Sima Bahrami, Mehrnaz Asadi Gharabaghi, Parisa Rezaeifar, Zahra Vakilazad
Publikováno v:
Clinical Case Reports, Vol 9, Iss 6, Pp n/a-n/a (2021)
Abstract Good's syndrome is a rare adult‐onset thymoma‐associated immunodeficiency with unknown pathogenesis. Therefore, it should be carefully managed as soon as possible when complications are presented. Because of variety of immunodeficiency,
Externí odkaz:
https://doaj.org/article/e041653d699648199cb7ce75494df060
Autor:
Saba Arshi, Sepideh Darougar, Mohammad Nabavi, Mohammad Hassan Bemanian, Morteza Fallahpour, Sima Shokri, Javad Ahmadian, Rasool Molatefi, Mahsa Rekabi, Zeinab Moinfar, Paniz Hashemitari, Narges Eslami
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 3 (2021)
Asthmatic patients may have aspirin-exacerbated respiratory disease and experience acute dyspnea and nasal symptoms within 3 hours after the ingestion of aspirin. This study aimed to evaluate the effect and outcome of daily low-dose aspirin in the tr
Externí odkaz:
https://doaj.org/article/26195a67cb7f479baa9edb07261293da
Autor:
Fereshteh Salari, Leila Bani Adam, Saba Arshi, Mohammad Hassan Bemanian, Morteza Fallahpour, Mohammad Nabavi
Publikováno v:
Journal of Pediatrics Review, Vol 7, Iss 4, Pp 223-228 (2019)
Introduction: Netherton Syndrome (NS) is a rare hereditary autosomal recessive disorder with ichthyosiform cutaneous lesions, specific hair shaft defect, and atopic diathesis. The incidence of NS is estimated to be approximately 1 in 200000. The obje
Externí odkaz:
https://doaj.org/article/4f57275d71b74b2f93acb18eb8a7ac05
Autor:
Mohammad Hassan Bemanian, Saba Arshi, Mohammad Nabavi, Mohammad Vafaee-Shahi, Morteza Fallahpour, Sima Shokri, Afshin Rezaeifar, Hossein Shahzadi, Fatemeh Atashrazm
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 2 (2021)
Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome is a rare primary immunodeficiency disorder characterized by recurrent infections and low immunoglobulin levels due to variable combined immunodeficiency, and centromeric
Externí odkaz:
https://doaj.org/article/e9f9c4e763e64b26b2ea20b0d1a7380f
Autor:
Mohammad Nabavi, Sima Bahrami, Saba Arshi, Afshin Rezaeifar, Mohammad Hassan Bemanian, Morteza Fallahpour, Sima Shokri, Homan Tehrani
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 1 (2021)
Hereditary angioedema (HAE) is characterized by recurrent attacks of skin and mucosal swelling in any part of the body including the digestive and respiratory tract which generally improve spontaneously within 12-72 hours. The underlying mechanism in
Externí odkaz:
https://doaj.org/article/a7a2a48fa1e14006bfb922bf66b44391