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Hydroxyurea responsiveness in β-thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity.
Pourfarzad F, von Lindern M, Azarkeivan A, Hou J, Kia SK, Esteghamat F, van Ijcken W, Philipsen S, Najmabadi H, Grosveld F. Pourfarzad F, et al. Among authors: azarkeivan a. Haematologica. 2013 May;98(5):696-704. doi: 10.3324/haematol.2012.074492. Epub 2012 Oct 25. Haematologica. 2013. PMID: 23100274 Free PMC article.
Simultaneous Hepatitis C Virus Genotyping and Variant Detection in Patients with Thalassemia: A Single-Center Phylogenetic Study.
Safarnezhad Tameshkel F, Karbalaie Niya MH, Zamani F, Ajdarkosh H, Khoonsari M, Faraji AH, Motamed N, Nikkhah M, Ameli M, Miri SM, Azarkeivan A, Sohrabi MR, Keyvani H. Safarnezhad Tameshkel F, et al. Among authors: azarkeivan a. Middle East J Dig Dis. 2022 Jan;14(1):124-130. doi: 10.34172/mejdd.2022.265. Epub 2022 Jan 30. Middle East J Dig Dis. 2022. PMID: 36619727 Free PMC article.
Elucidating the spectrum of alpha-thalassemia mutations in Iran.
Hadavi V, Taromchi AH, Malekpour M, Gholami B, Law HY, Almadani N, Afroozan F, Sahebjam F, Pajouh P, Kariminejad R, Kariminejad MH, Azarkeivan A, Jafroodi M, Tamaddoni A, Puehringer H, Oberkanins C, Najmabadi H. Hadavi V, et al. Among authors: azarkeivan a. Haematologica. 2007 Jul;92(7):992-3. doi: 10.3324/haematol.10658. Haematologica. 2007. PMID: 17606454 Free article.
Molecular mechanisms underlying thalassemia intermedia in Iran.
Neishabury M, Azarkeivan A, Oberkanins C, Esteghamat F, Amirizadeh N, Najmabadi H. Neishabury M, et al. Among authors: azarkeivan a. Genet Test. 2008 Dec;12(4):549-56. doi: 10.1089/gte.2008.0018. Genet Test. 2008. PMID: 18939939
alpha-thalassemia mutations in Khuzestan Province, Southwest Iran.
Zandian K, Nateghi J, Keikhaie B, Pedram M, Hafezi-Nejad N, Hadavi V, Oberkanins C, Azarkeivan A, Law HY, Najmabadi H. Zandian K, et al. Among authors: azarkeivan a. Hemoglobin. 2008;32(6):546-52. doi: 10.1080/03630260802532780. Hemoglobin. 2008. PMID: 19065332
Frequency of positive XmnIGgamma polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation.
Neishabury M, Azarkeivan A, Najmabadi H. Neishabury M, et al. Among authors: azarkeivan a. Blood Cells Mol Dis. 2010 Mar-Apr;44(2):95-9. doi: 10.1016/j.bcmd.2009.10.007. Epub 2009 Nov 4. Blood Cells Mol Dis. 2010. PMID: 19892574
104 results