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Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia.
Fallah MS, Zadeh-Vakili A, Aleyasin SA, Mahdian R, Karimipour M, Raeisi M, Jamali S, Ebrahimi A, Fooladi P, Naderi M, Baysal E, Zeinali S. Fallah MS, et al. Blood Cells Mol Dis. 2009 Sep-Oct;43(2):158-60. doi: 10.1016/j.bcmd.2009.05.006. Epub 2009 Jul 3. Blood Cells Mol Dis. 2009. PMID: 19577494 No abstract available.
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.
Shirzadeh T, Saeidian AH, Bagherian H, Salehpour S, Setoodeh A, Alaei MR, Youssefian L, Samavat A, Touati A, Fallah MS, Vahidnezhad H, Karimipoor M, Azadmehr S, Raeisi M, Bandehi Sarhadi A, Zafarghandi Motlagh F, Jamali M, Zeinali Z, Abiri M, Zeinali S; Additional individual contributors. Shirzadeh T, et al. Among authors: fallah ms. J Inherit Metab Dis. 2018 Nov;41(6):1159-1167. doi: 10.1007/s10545-018-0228-6. Epub 2018 Aug 29. J Inherit Metab Dis. 2018. PMID: 30159852
Heterogeneity of hemoglobin h disease in childhood.
Zeinali S, Fallah MS, Bagherian H. Zeinali S, et al. Among authors: fallah ms. N Engl J Med. 2011 May 26;364(21):2070-1; author reply 2071. doi: 10.1056/NEJMc1103406. N Engl J Med. 2011. PMID: 21612484 No abstract available.
Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran.
Sharifi Z, Taheri M, Fallah MS, Abiri M, Golnabi F, Bagherian H, Zeinali R, Farahzadi H, Alborji M, Tehrani PG, Amini M, Asnavandi S, Hashemi M, Forouzesh F, Zeinali S. Sharifi Z, et al. Among authors: fallah ms. J Mol Neurosci. 2021 Nov;71(11):2281-2298. doi: 10.1007/s12031-020-01789-0. Epub 2021 Jan 22. J Mol Neurosci. 2021. PMID: 33481221
77 results