| 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 | 124 | 2011 |
| 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 | 28 | 2013 |
| Evaluation of the Persian version of modified fatigue impact scale in Iranian patients with multiple sclerosis MH Harirchian, S Nasergivechi, M Maddah, A Meysamie, H Amini, ... Iranian journal of neurology 12 (1), 32, 2013 | 25 | 2013 |
| Weaning and extubation from neonatal mechanical ventilation: an evidenced-based review R Sangsari, M Saeedi, M Maddah, K Mirnia, JP Goldsmith BMC pulmonary medicine 22 (1), 421, 2022 | 23 | 2022 |
| 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 | 19 | 2012 |
| Interleukin 10 and transforming growth factor beta 1 gene polymorphisms in juvenile idiopathic arthritis. S Harsini, V Ziaee, M Maddah, A Rezaei, M Sadr, S Zoghi, ... Bratislavske lekarske listy 117 (5), 258-262, 2016 | 17 | 2016 |
| IL23R gene polymorphism with juvenile idiopathic arthritis and its association with serum IL‐17A S Emami, V Ziaee, A Rezaei, M Sadr, M Maddah, AA Amirzargar, ... International Journal of Rheumatic Diseases 19 (11), 1189-1196, 2016 | 15 | 2016 |
| Association of Interleukin-2, but not Interferon-Gamma, single nucleotide polymorphisms with juvenile idiopathic arthritis M Maddah, S Harsini, A Rezaei, M Sadr, S Zoghi, MH Moradinejad, ... Allergologia et immunopathologia 44 (4), 303-306, 2016 | 14 | 2016 |
| Association of interleukin-1 family gene polymorphisms with juvenile idiopathic arthritis in Iranian population V Ziaee, M Maddah, S Harsini, A Rezaei, M Sadr, S Zoghi, ... Allergologia et immunopathologia 44 (6), 542-546, 2016 | 12 | 2016 |
| Association of interleukin-6 single nucleotide polymorphisms with juvenile idiopathic arthritis V Ziaee, M Maddah, MH Moradinejad, A Rezaei, S Zoghi, M Sadr, ... Clinical rheumatology 36, 77-81, 2017 | 11 | 2017 |
| Polymorphisms of genes encoding interleukin-4 and its receptor in Iranian patients with juvenile idiopathic arthritis V Ziaee, A Rezaei, S Harsini, M Maddah, S Zoghi, M Sadr, ... Clinical rheumatology 35, 1943-1948, 2016 | 11 | 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 | 8 | 2019 |
| Association of tumour necrosis factor‐alpha G/A‐238 and G/A‐308 single nucleotide polymorphisms with juvenile idiopathic arthritis M Maddah, S Harsini, V Ziaee, MH Moradinejad, A Rezaei, S Zoghi, ... International Journal of Immunogenetics 43 (6), 391-396, 2016 | 8 | 2016 |
| 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 | 6 | 2020 |
| Association of Interleukin-6 single nucleotide polymorphisms with juvenile idiopathic arthritis S Harsini, V Ziaee, M Maddah, MH Moradinejad, A Rezaei, S Zoghi, ... Journal of Allergy and Clinical Immunology 139 (2), AB207, 2017 | 1 | 2017 |
| Serum Vitamin D Levels in Premature Neonates with Retinopathy of Prematurity; Prevalence, Severity, and Types of Treatments; A Cross-Sectional Study from Iran, 2019-2020. Z Mosayebi, S Sagheb, MR Zarkesh, M Maddah, M Shariat Iranian Journal of Neonatology 16 (1), 2025 | | 2025 |
| Comparison of the Effectiveness of Pharmacological and Non-Pharmacological Methods in Reducing the Pain of Retinopathy of Prematurity Examination MK Shariati, AD Farahani, NT Taleghani, F Palizban, A Naseh, M Maddah, ... Novelty in Biomedicine 12 (3), 104-109, 2024 | | 2024 |
| The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child SZ Modarresi, S Tajik, M Badalzadeh, MR Fazlollahi, M Houshmand, ... Iranian Journal of Allergy, Asthma and Immunology, 2023 | | 2023 |
| Association of tumor necrosis factor-alpha G/A-238 and G/A-308 single nucleotide polymorphisms with juvenile idiopathic arthritis M Maddah, S Harsini, V Ziaee, MH Moradinejad, F Tahghighi, A Rezaei, ... ALLERGY 71, 430-430, 2016 | | 2016 |
| Consecutive Siblings Affected with Autosomal Recessive Chronic Granulomatous Disease and its Relevance to Consanguineous Marriages S Modarresi, Z Pourpak, MR Fazlollahi, M Reza, M Hooshmand, ... JOURNAL OF CLINICAL IMMUNOLOGY 32 (2), 375-375, 2012 | | 2012 |
Mohammad Reza FazlollahiImmunology, Asthma and Allergy Research Institute,Tehran University of Medical SciencesE-mailová adresa ověřena na: sina.tums.ac.ir