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, 792-801, 2011 | 117 | 2011 |
Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran M Nourizadeh, L Shakerian, S Borte, M Fazlollahi, M Badalzadeh, ... Scandinavian Journal of Immunology 88 (2), e12699, 2018 | 42 | 2018 |
Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease* S Teimourian, E Zomorodian, M Badalzadeh, AR Pouya, ... British journal of haematology 141 (6), 848-851, 2008 | 29 | 2008 |
Clinical, Laboratory and Molecular Findings of 63 Patients with Severe Combined Immunodeficiency. A Decade s Experience MR Fazlollahi, Z Pourpak, AA Hamidieh, M Movahedi, M Houshmand, ... J Investig Allergol Clin Immunol 27 (5), 299-304, 2017 | 27 | 2017 |
A new patient with inherited TYK2 deficiency SA Sarrafzadeh, M Mahloojirad, JL Casanova, M Badalzadeh, ... Journal of clinical immunology 40, 232-235, 2020 | 24 | 2020 |
Molecular diagnosis of X-linked chronic granulomatous disease in Iran S Teimourian, Z Rezvani, M Badalzadeh, C Kannengiesser, D Mansouri, ... International journal of hematology 87, 398-404, 2008 | 24 | 2008 |
Genetic and molecular findings of 38 Iranian patients with chronic granulomatous disease caused by p47‐phox defect S Tajik, M Badalzadeh, MR Fazlollahi, M Houshmand, N Bazargan, ... Scandinavian journal of immunology 90 (1), e12767, 2019 | 17 | 2019 |
Molecular, immunological, and clinical features of 16 Iranian patients with Mendelian susceptibility to mycobacterial disease SA Sarrafzadeh, M Nourizadeh, M Mahloojirad, MR Fazlollahi, ... Journal of Clinical Immunology 39, 287-297, 2019 | 16 | 2019 |
Investigation of ITGB2 gene in 12 new cases of leukocyte adhesion deficiency-type I revealed four novel mutations from Iran FT Mortezaee, B Esmaeli, M Badalzadeh, M Ghadami, MR Fazlollahi, ... Archives of Iranian Medicine 18 (11), 0-0, 2015 | 16 | 2015 |
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 & Immunology 11 (4), 2012 | 16 | 2012 |
Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency N Parvaneh, S Teimourian, G Jacomelli, M Badalzadeh, M Bertelli, ... Clinical biochemistry 4 (41), 350-352, 2008 | 16 | 2008 |
Three novel mutations in CYBA among 22 Iranians with Chronic granulomatous disease M Badalzadeh, S Tajik, MR Fazlollahi, M Houshmand, F Fattahi, ... International journal of immunogenetics 44 (6), 314-321, 2017 | 9 | 2017 |
A novel CYBB mutation in chronic granulomatous disease in Iran S Tajik, M Badalzadeh, MR Fazlollahi, M Houshmand, F Zandieh, ... Iranian Journal of Allergy, Asthma and Immunology, 426-429, 2016 | 8 | 2016 |
Lupus erythematosus and chronic granulomatous disease: report of four Iranian patients with AR-CGD and one XL-CGD M Maddah, MR Fazlollahi, R Shiari, F Shahram, S Mamishi, D Babaie, ... Iranian Journal of Allergy, Asthma and Immunology, 2019 | 7 | 2019 |
In vitro analysis of nine microRNAs in CD8+ T cells of asthmatic patients and the effects of two FDA-approved drugs M Badalzadeh, M Mazinani, Z Pourpak, H Heidarnazhad, E Mortaz, ... Iranian Journal of Allergy, Asthma and Immunology, 358-368, 2019 | 6 | 2019 |
Investigating the variation of TREC/KREC in combined immunodeficiencies L Shakerian, M Nourizadeh, M Badalzadeh, MR Fazlollahi, ... Iranian Journal of Allergy, Asthma and Immunology 20 (4), 402-412, 2021 | 5 | 2021 |
The critical role of prenatal genetic study in prevention of primary immunodeficiency in high-risk families: the largest report of 107 cases SZ Modarresi, N Sabetkish, M Badalzadeh, S Tajik, B Esmaeili, ... Iranian Journal of Allergy, Asthma and Immunology, 2020 | 4 | 2020 |
Clinical, immunological and molecular findings of 8 patients with typical and atypical severe combined immunodeficiency: identification of 7 novel mutations by whole exome … Z Alizadeh, MR Fazlollahi, M Mazinani, M Badalzadeh, H Heydarlou, ... Genes & Immunity 24 (4), 207-214, 2023 | 1 | 2023 |
Identification of a 53 kDa protein, as a new high molecular weight allergen from Fraxinusexcelsior (Ash) pollen M Sharif Shoushtari, A Majd, MA Assarehzadegan, S Fanuel, M Moin, ... Allergo Journal International 29, 233-239, 2020 | 1 | 2020 |
Determining reference ranges for lymphocyte proliferation responses to phytohemagglutinin and Bacillus Calmette–Guérin in Iranian children M Nourizadeh, SA Sarrafzadeh, RS Shoormasti, MR Fazlollahi, S Saghafi, ... Clinical Immunology, 109937, 2024 | | 2024 |