Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mehdi Ghaini"'
Autor:
Seyed Alireza Mahdaviani, Majid Marjani, Mahnaz Jamee, Armin Khavandegar, Hosseinali Ghaffaripour, Golnaz Eslamian, Mehdi Ghaini, Shabnam Eskandarzadeh, Jean-Laurent Casanova, Jacinta Bustamante, Davood Mansouri, Ali Akbar Velayati
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 3 (2021)
Mendelian susceptibility to mycobacterial disease (MSMD) is a rare group of genetic disorders characterized by infections with weakly virulent environmental mycobacteria (EM) or Mycobacterium bovis bacillus Calmette-Guérin (BCG). Herein, we describe
Externí odkaz:
https://doaj.org/article/fb943d76aba14a82a0953d0b056ace37
Autor:
Mahsa Eskian, Payam Tabarsi, Mahshid Movahedi, Mehrnaz Mesdaghi, Mihan Poorabdolah, Abdollah Karimi, Parisa Farnia, Davood Mansouri, Majid Zaki-Dizaji, Mehdi Ghaini, Jean-Laurent Casanova, Ali Akbar Velayati, Majid Marjani, Zahra Chavoshzadeh, MirHojjat Khorasanizadeh, Nima Rezaei, Jacinta Bustamante, Hosseinali Ghaffaripour, Shabnam Eskandarzadeh, Seyed Alireza Mahdaviani, Maryam Hassanzad, Karim Rahimi Aghdam, Nooshin Baghaie, Farzad Noori, Shahram Kahkooi, Mahnaz Jamee, Stéphanie Boisson-Dupuis, Mahboubeh Mansouri, Esmail Mortaz, Afshin Moniri
Publikováno v:
Journal of Clinical Immunology. 40:872-882
Mendelian susceptibility to mycobacterial diseases (MSMD) is a rare congenital condition characterized by a selective predisposition to infections caused by weakly virulent mycobacteria and other types of intra-macrophagic pathogens. The 16 genes ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e104f0e204bb5c9db69a23319cd7dc6a
https://doi.org/10.1007/s10875-020-00813-7
https://doi.org/10.1007/s10875-020-00813-7
Autor:
Javad Enayat, Sayed Alireza Mahdaviani, Mahsa Rekabi, Mehdi Ghaini, Golnaz Eslamian, Mazdak Fallahi, Sepideh Ghazvineh, Niusha Sharifinejad, Mohammad Reza Raoufy, Ali Akbar Velayati
Publikováno v:
Respiratory physiologyneurobiology. 300
The intensity of respiratory symptoms and expiratory airflow limitations in asthma fluctuate over time. Some studies have reported variable complexity of the respiratory patterns in asthmatic patients. Thus, we conducted a novel study to assess the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14f05dc9de7d1df695aca92cd7617914
https://pubmed.ncbi.nlm.nih.gov/35217233
https://pubmed.ncbi.nlm.nih.gov/35217233
Autor:
Mahshid Movahedi, Mahnaz Jamee, Hosseinali Ghaffaripour, Farzad Noori, Mehdi Ghaini, Shabnam Eskandarzadeh, Javad Enayat, Golnaz Eslamian, Guitti Pourdowlat, Niusha Sharifinejad, Mihan Poorabdollah, Seyed Alireza Nadji, Mazdak Fallahi, Zahra Daneshmandi, Jalal Heshmatnia, Alireza Eslaminejad, Atefeh Fakharian, Maryam Vasheghani, Afshin Moniri, Maryam Sadat Mirenayat, Payam Tabarsi, Majid Marjani, Nima Rezaei, Mikko R. J. Seppänen, Davood Mansouri, Seyed Alireza Mahdaviani, Ali Akbar Velayati
Publikováno v:
Allergologia et immunopathologia. 50(1)
Background: Inborn errors of immunity (IEIs) are a group of congenital diseases caused by genetic defects in the development and function of the immune system. The involvement of the respiratory tract is one of the most common presentations in IEIs.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::749a1329cb9bd887f04aa0679190cf9f
https://pubmed.ncbi.nlm.nih.gov/34935317
https://pubmed.ncbi.nlm.nih.gov/34935317
Autor:
Saeed Sadr, Mehrnaz Mesdaghi, Shabnam Eskandarzadeh, Bernice Lo, Mahnaz Jamee, Mohammad Keramatipour, Zahra Chavoshzadeh, Mohammad Taghi Arzanian, Bibi Shahin Shamsian, Mehdi Ghaini, Pejman Rohani
LPS-responsive beige-like anchor protein (LRBA) deficiency is a monogenic primary immunodeficiency characterized by a heterogeneous spectrum of clinical manifestations associated with immune dysregulation. In this study, we reported clinical, immunol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::208df6e089411a0c30691d9d1c4b0f4d
Autor:
Mehrnaz Mesdaghi, Javad Enayat, Seyed Alireza Mahdaviani, Mahsa Rekabi, Mohammadreza Hosseini Abajalou, Delara Babaei, William Rae, Habib Emami, Zahra Chavoshzadeh, Golnaz Eslamian, Shaya Doustkhah, Shabnam Eskandarzadeh, Narges Eslami, Mehdi Ghaini, Mahboubeh Mansouri, Mahnaz Jamee
Publikováno v:
International archives of allergy and immunology. 182(11)
Introduction: Inborn errors of immunity (IEIs) are rare inherited disorders with a broad spectrum of manifestations. Here, we aimed to delineate the atopy burden in a cohort of patients with IEIs. Methods: 313 patients with IEIs were enrolled in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c06c7d30d91f932d19f3814e37fa31a1
https://pubmed.ncbi.nlm.nih.gov/34058734
https://pubmed.ncbi.nlm.nih.gov/34058734
Autor:
Mehdi Ghaini, Davood Mansouri, Hosseinali Ghaffaripour, Jacinta Bustamante, Golnaz Eslamian, Jean-Laurent Casanova, Armin Khavandegar, Majid Marjani, Mahnaz Jamee, Seyed Alireza Mahdaviani, Shabnam Eskandarzadeh, Ali Akbar Velayati
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 3 (2021)
Mendelian susceptibility to mycobacterial disease (MSMD) is a rare group of genetic disorders characterized by infections with weakly virulent environmental mycobacteria (EM) or Mycobacterium bovis bacillus Calmette-Guérin (BCG). Herein, we describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05a7f2ee0878a44021a6ed4cc9285892
https://doi.org/10.22541/au.158999368.80817405
https://doi.org/10.22541/au.158999368.80817405
Autor:
Mahnaz Jamee, Davood Mansouri, Gholamreza Azizi, Nematollah Joneidi, Mehdi Ghaini, Shabnam Eskandarzade, Ali Akbar Velayati, Majid Marjani, Mélanie Migaud, Jl Casanova, Anne Puel, Afshin Moniri, Seyed Alireza Mahdaviani, Hosseinali Ghaffaripour
Publikováno v:
Immunological investigations. 49(3)
Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) syndrome is a rare monogenic autosomal recessive disorder caused by biallelic mutations in the AIRE (autoimmune regulator) gene. Patients with APECED present with heterogeneous e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e849a602a2a69d958f311f3d14854208
https://pubmed.ncbi.nlm.nih.gov/31588815
https://pubmed.ncbi.nlm.nih.gov/31588815