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Pediatric Hematology and Oncology|December 24, 2021
Clinical and genetic characteristics of hemoglobin H disease in IranHassan Abolghasemi, Sharareh Kamfar, Azita Azarkeivan, et al.
International Journal of Hematology-Oncology and Stem Cell Research|December 9, 2016
Secondary ALL after Successful Treatment of Ewing's Sarcoma: A Case ReportKourosh Goudarzi Pour, Samin Alavi, Shahin Shamsian, et al.
The Korean Journal of Hematology|July 13, 2011
Clinical outcomes of Torque teno virus-infected thalassemic patients with and without hepatitis C virus infectionSamin Alavi, Zohreh Sharifi, Ali Kord Valeshabad, et al.
Pediatric Hematology and Oncology|August 30, 2008
Sensory neural hearing loss in beta-thalassemia major patients treated with deferoxamineBibi Shahin Shamsian, Ali Aminasnafi, Habiballah Moghadassian, et al.
Pediatric Hematology and Oncology|April 6, 2012
Primary hemophagocytic lymphohistiocytosis in Iran: report from a single referral centerBibi Shahin Shamsian, Nima Rezaei, Samin Alavi, et al.
Iranian Journal of Allergy, Asthma, and Immunology|December 25, 2012
Detection of six novel mutations in WASP gene in fifteen Iranian Wiskott-Aldrich patientsSepideh Safaei, Mohammad Reza Fazlollahi, Masoud Houshmand, et al.
Iranian Journal of Allergy, Asthma, and Immunology|September 11, 2008
Autosomal recessive chronic granulomatous disease, IgA deficiency and refractory autoimmune thrombocytopenia responding to Anti-CD20 monoclonal antibodyBibi Shahin Shamsian, Davoud Mansouri, Zahra Pourpak, et al.
The Turkish Journal of Pediatrics|May 4, 2011
A 10-year single center survey of pediatric patients with histiocytic disorders in IranBibi Shahin Shamsian, Maryam Nikoufar, Shadi Abdar Esfahani, et al.
Annals of Hematology|February 11, 2025
A randomized, two-armed, double-blind, single-dose, cross-over, bioequivalence clinical trial to compare pharmacokinetic parameters and safety of recombinant human factor VIII with Fc fusion produced by AryoGen Pharmed Company versus Elocta<sup>®</sup> (reference product) in previously treated patients with severe haemophilia AAziz Eghbali, Peyman Eshghi, Gholamreza Toogeh, et al.
Immunologic Research|May 24, 2025
A novel variant in the STIM1 gene leading to combined immunodeficiency and congenital myopathyAmirreza Taherkhani, Mahmood Gorjizad, Farzad Ahmadabadi, et al.
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