Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Najmeddin Kalantari"'
Autor:
Nima Rezaei, Raif S. Geha, Hassan Abolhassani, Capucine Picard, Asghar Aghamohammadi, Iraj Mohammadzadeh, Lennart Hammarström, Alireza Ghajar, Najmeddin Kalantari, Wayne Bainter, Mahmood Tavassoli, Farahzad Jabbari-Azad, Reza Amin, Delara Babaie, Habib Soheili, Mohammad Hossein Eslamian, Mehrnaz Mesdaghi, Janet Chou, Nima Parvaneh, Sevgi Keles, Arash Havaei, Craig D. Platt, Taher Cheraghi, Mohammamd Nabavi, Masoud Movahedi, Talal A. Chatila, Mohammad Taghi Joghataei, Michel J. Massaad, Mohsen Afarideh, Javad Mohammadi, Mohammad Hassan Bemanian, Zahra Chavoshzadeh, Hamid Ahanchian, Soheila Aleyasin, Alireza Shafiei, Mohammad Gharagozlou, Seyed Hamidreza Mortazavi, Babak Negahdari, Basel K. al-Ramadi, Amir Ali Hamidieh, Javad Tafaroji, Mahboubeh Mansouri, Seyed Alireza Mahdaviani, Saba Arshi, Rasol Molatefi, Reza Faridhosseini, Tooba Momen, Mohsen Ghadami, Rasoul Nasiri Kalmarzi, Maryam Khoshkhui, Marzieh Tavakol, Roya Sherkat, Afshin Shirkani, Nasrin Behniafard, Abbas Dabbaghzadeh, Reza Yazdani, Gholamreza Azizi, Abbas Khalili, Javad Ghaffari
Publikováno v:
Journal of Allergy and Clinical Immunology. 141:1450-1458
Background Combined immunodeficiencies (CIDs) are diseases of defective adaptive immunity with diverse clinical phenotypes. Although CIDs are more prevalent in the Middle East than Western countries, the resources for genetic diagnosis are limited. O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::715b8af525ae077852802067ee57b227
https://doi.org/10.1016/j.jaci.2017.06.049
https://doi.org/10.1016/j.jaci.2017.06.049
Autor:
Mohammad Reza Fazlollahi, Leyla Sedighipour, Mohsen Badalzadeh, Marzieh Maddah, Ghamar Taj Khotaei, Iraj Mohammadzadeh, Fatemeh Fattahi, Zahra Chavoshzadeh, Fatemeh Behmanesh, Mostafa Moin, Masoud Movahedi, Nasrin Bazargan, Zahra Pourpak, Mohammad Hassan Bemanian, S D Mansouri, Shaghayegh Tajik, Seyed Alireza Mahdaviani, Setareh Mamishi, Seyed Ahmad Tabatabaei, Najmeddin Kalantari, Fariborz Zandieh, Amir Ali Hamidieh
Publikováno v:
Journal of Clinical Immunology, 31(5), 792-801. SPRINGER/PLENUM PUBLISHERS
Chronic granulomatous disease (CGD) is a rare immunodeficiency due to a genetic defect in one of the NADPH-oxidase components. We studied CGD inheritance forms (autosomal recessive (AR) or X-linked (XL)) and AR-CGD subtypes in Iran.Clinical and funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba3ccf3360d376cf9a6031682bb6a70c
https://doi.org/10.1007/s10875-011-9567-x
https://doi.org/10.1007/s10875-011-9567-x