Biblio

Author Title Type [ Year(Desc)]
Filters: Author is Badalzadeh, Mohsen  [Clear All Filters]
2019
Maddah M, Fazlollahi MReza, Shiari R, Shahram F, Mamishi S, Babaie D, Monajemzadeh M, Sotudeh S, Hamidieh AAli, Badalzadeh M, et al. Lupus Erythematosus and Chronic Granulomatous Disease: Report of Four Iranian Patients with AR-CGD and One XL-CGD. Iran J Allergy Asthma Immunol. 2019;18(4):452-458.
2022
Vaezi M, Souri M, Setarehdan SAmin, Hamidieh AAli, Fazlollahi MReza, Pourpak Z, Badalzadeh M, Tajik S, Mahdaviani SAlireza, Alimoghaddam K, et al. A fludarabine and melphalan reduced-intensity conditioning regimen for HSCT in fifteen chronic granulomatous disease patients and a literature review. Ann Hematol. 2022.
2023
Fazlollahi MReza, Hamidieh AAli, Moradi L, Shoormati RShokouhi, Sabetkish N, Esmaeili B, Badalzadeh M, Alizadeh Z, Shamlou S, Movahedi M, et al. Clinical and immunological characteristics of 69 leukocyte adhesion deficiency-I patients. Pediatr Allergy Immunol. 2023;34(7):e13990.
Tajik S, Badalzadeh M, Houshmand M, Alizadeh Z, Moradi L, Hamidieh AAli, Shafiei A, Heris JAhmadiani, Bahram S, Molitor A, et al. Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient. Scand J Immunol. 2023;97(5):e13264.
Alizadeh Z, Badalzadeh M, Heydarlou H, Shakerian L, Rad MMahlooji, Zandieh F, Fazlollahi MReza. Purine Nucleoside Phosphorylase Deficiency in Two Unrelated Patients with Autoimmune Hemolytic Anemia and Eosinophilia: Two Novel Mutations. Arch Iran Med. 2023;26(12):712-716.