Mohammad Reza Fazlollahi
Mohammad Reza Fazlollahi
Immunology, Asthma and Allergy Research Institute,Tehran University of Medical Sciences
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TitleCited byYear
Gastrointestinal manifestations in patients with common variable immunodeficiency
A Khodadad, A Aghamohammadi, N Parvaneh, N Rezaei, F Mahjoob, ...
Digestive diseases and sciences 52 (11), 2977-2983, 2007
Inheritance pattern and clinical aspects of 93 Iranian patients with chronic granulomatous disease
F Fattahi, M Badalzadeh, L Sedighipour, M Movahedi, MR Fazlollahi, ...
Journal of clinical immunology 31 (5), 792, 2011
Clinical and laboratory findings in Iranian patients with leukocyte adhesion deficiency (study of 15 cases)
M Movahedi, N Entezari, Z Pourpak, S Mamishi, Z Chavoshzadeh, ...
Journal of clinical immunology 27 (3), 302-307, 2007
Common causes of anaphylaxis in children: the first report of anaphylaxis registry in Iran
S Barzegar, A Rosita, Z Pourpak, MH Bemanian, R Shokouhi, M Mansouri, ...
World Allergy Organization Journal 3 (1), 9-13, 2010
Analysis of RAB27A gene in Griscelli syndrome type 2: novel mutations including a deletion hotspot
S Mamishi, MH Modarressi, B Pourakbari, B Tamizifar, F Mahjoub, ...
Journal of clinical immunology 28 (4), 384-389, 2008
Understanding adverse drug reactions and drug allergies: principles, diagnosis and treatment aspects
Z Pourpak, MR Fazlollahi, F Fattahi
Recent patents on inflammation & allergy drug discovery 2 (1), 24-46, 2008
Reduced-intensity conditioning hematopoietic SCT for pediatric patients with LAD-1: clinical efficacy and importance of chimerism
AA Hamidieh, Z Pourpak, M Hosseinzadeh, MR Fazlollahi, ...
Bone marrow transplantation 47 (5), 646-650, 2012
Allergy to human insulin and specific immunotherapy with glargine; case report with review of literature
S Hasani-Ranjbar, MR Fazlollahi, A Mehri, B Larijani
Acta diabetologica 49 (1), 69-73, 2012
Two cases of syndromic neutropenia with a report of novel mutation in G6PC3
Z Alizadeh, MR Fazlollahi, P Eshghi, AA Hamidieh, M Ghadami, ...
Neutropenia in patients with primary antibody deficiency disorders
N Rezaei, A Farhoudi, Z Pourpak, A Aghamohammadi, M Moin, ...
Iranian Journal of Allergy, Asthma and Immunology, 77-82, 2004
Different pattern of gene mutations in Iranian patients with severe congenital neutropenia (including 2 new mutations).
Z Alizadeh, MR Fazlollahi, M Houshmand, M Maddah, Z Chavoshzadeh, ...
Iranian Journal of Allergy, Asthma and Immunology, 86-92, 2013
Cow’s milk anaphylaxis in children first report of Iranian Food Allergy Registry
P Teymourpour, Z Pourpak, MR Fazlollahi, S Barzegar, R Shokouhi, ...
Iranian Journal of Allergy, Asthma and Immunology, 29-36, 2012
Hematopoietic stem cell transplantation with a reduced‐intensity conditioning regimen in pediatric patients with G riscelli syndrome type 2
AA Hamidieh, Z Pourpak, K Yari, MR Fazlollahi, S Hashemi, M Behfar, ...
Pediatric transplantation 17 (5), 487-491, 2013
Prevention and control of infections in patients with severe congenital neutropenia; a follow up study
T Salehi, MR Fazlollahi, M Maddah, M Nayebpour, MT Yazdi, Z Alizadeh, ...
Iranian Journal of Allergy, Asthma and Immunology, 51-56, 2012
The prevalence of asthma in Iranian adults: the first national survey and the most recent updates
MR Fazlollahi, M Najmi, M Fallahnezhad, N Sabetkish, A Kazemnejad, ...
The clinical respiratory journal 12 (5), 1872-1881, 2018
Prevalence of asthma symptoms and smoking behavior among 20-44 years old adults in Tehran: A telephone survey
B Tazesh, A Shaabani, MR Fazlollahi, A Entezari, R Dashti, Z Pourpak, ...
Scientific Research Publishing, 2013
Molecular analysis of four cases of chronic granulomatous disease caused by defects in NCF-2: the gene encoding the p67-phox.
M Badalzadeh, F Fattahi, MR Fazlollahi, S Tajik, MH Bemanian, ...
Iranian Journal of Allergy, Asthma and Immunology, 340-344, 2012
The prevalence of allergic rhinitis, allergic conjunctivitis, atopic dermatitis and asthma among adults of Tehran
RS SHOORMASTI, Z Pourpak, MR Fazlollahi, A Kazemnejad, F Nadali, ...
Iranian journal of public health 47 (11), 1749, 2018
DOCK2 deficiency in a patient with hyper IgM phenotype
Z Alizadeh, M Mazinani, L Shakerian, M Nabavi, MR Fazlollahi
Journal of clinical immunology 38 (1), 10-12, 2018
A new IL-2RG gene mutation in an X-linked SCID identified through TREC/KREC screening: a case report
M Nourizadeh, S Borte, MR Fazlollahi, L Hammarström, Z Pourpak
Iranian Journal of Allergy, Asthma and Immunology 14 (4), 457-461, 2015
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