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Transfusion Medicine (Oxford, England)|March 25, 2015
Combination therapy - deferasirox and deferoxamine - in thalassemia major patients in emerging countries with limited resourcesN Arandi, S Haghpanah, S Safaei, et al.Healthcare (Basel, Switzerland)|January 25, 2025
Multidimensional Demographic Analyses of COVID-19 Vaccine Inequality in the United States: A Systematic ReviewSeyed M Karimi, Sirajum Munira Khan, Mana Moghadami, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|August 23, 2011
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in IranM Karimi, A Vafafar, S Haghpanah, et al.Anticancer Research|February 5, 2020
Aggressive Local Control With Multisite Stereotactic Body Radiation in Metastatic Ewing Sarcoma: A Literature Review and Case ReportAhmad M Karimi, Shauna R Campbell, Shireen Parsai, et al.International Journal of Biomedical Science : IJBS|October 31, 2013
Cancer in pregnancy: a 10-year experience in shahid sadoughi hospital, yazd, iranM Karimi-Zarchi, M Ghane Ezabadi, S Hekmatimoghaddam, et al.Iranian Red Crescent Medical Journal|June 28, 2012
Combined α-thalassemia and Hemoglobin J-Iran (β77 His → Asp). A Family Study in southern IranS J Dehghani, A Amiri Dashtarzhen, Sh Nasirabadi, et al.Experimental Neurology|May 15, 2012
Dopamine pathway loss in nucleus accumbens and ventral tegmental area predicts apathetic behavior in MPTP-lesioned monkeysC A Brown, M C Campbell, M Karimi, et al.International Journal of Organ Transplantation Medicine|May 5, 2022
TET2, DNMT3A, IDH1, and JAK2 Mutation in Myeloproliferative Neoplasms in southern IranE Abedi, M Ramzi, M Karimi, et al.Acta Endocrinologica (Bucharest, Romania : 2005)|July 21, 2020
Frequency of thyroid nodules in patients with β-thalassemias in Southern IranS Haghpanah, P Pishdad, T Zarei, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|March 13, 2012
Retrospective evaluation of bleeding tendency and simultaneous thrombin and plasmin generation in patients with rare bleeding disordersM Van Geffen, M Menegatti, A Loof, et al.Pageof 24