|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, ...
IRANIAN JOURNAL OF ALLERGY, ASTHMA AND IMMUNOLOGY (IJAAI) 10 (3), 227-230, 2011
|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