Farashi S - Search Results

1

Frequency of α-Globin Gene Triplications and Coinheritance with β-Globin Gene Mutations in the Iranian Population.

Abedini SS, Forouzesh Pour F, Karimi K, Ghaderi Z, Farashi S, Tavakoli Koudehi A, Javadi Pirouz H, Mobini Nejad SB, Azarkeivan A, Najmabadi H. Abedini SS, et al. Among authors: farashi s. Hemoglobin. 2018 Jul;42(4):252-256. doi: 10.1080/03630269.2018.1526192. Epub 2018 Nov 19. Hemoglobin. 2018. PMID: 30451045

2

The XmnI and BCL11A single nucleotide polymorphisms may help predict hydroxyurea response in Iranian β-thalassemia patients.

Banan M, Bayat H, Azarkeivan A, Mohammadparast S, Kamali K, Farashi S, Bayat N, Khani MH, Neishabury M, Najmabadi H. Banan M, et al. Among authors: farashi s. Hemoglobin. 2012;36(4):371-80. doi: 10.3109/03630269.2012.691147. Epub 2012 Jun 11. Hemoglobin. 2012. PMID: 22686296

3

Novel mutations responsible for α-thalassemia in Iranian families.

Bayat N, Farashi S, Hafezi-Nejad N, Faramarzi N, Ashki M, Vakili S, Imanian H, Khosravi M, Azar-Keivan A, Najmabadi H. Bayat N, et al. Among authors: farashi s. Hemoglobin. 2013;37(2):148-59. doi: 10.3109/03630269.2013.763821. Epub 2013 Feb 12. Hemoglobin. 2013. PMID: 23402770

4

A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.

Farashi S, Faramarzi Garous N, Zeinali F, Vakili S, Ashki M, Imanian H, Najmabadi H, Azarkeivan A, Tamaddoni A. Farashi S, et al. Hemoglobin. 2015;39(3):196-200. doi: 10.3109/03630269.2015.1030757. Epub 2015 May 15. Hemoglobin. 2015. PMID: 25976776

5

Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient.

Farashi S, Faramarzi Garous N, Ashki M, Vakili S, Zeinali F, Imanian H, Azarkeivan A, Najmabadi H. Farashi S, et al. Hemoglobin. 2015;39(3):152-5. doi: 10.3109/03630269.2015.1027915. Epub 2015 May 15. Hemoglobin. 2015. PMID: 25976777

6

Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.

Farashi S, Bayat N, Faramarzi Garous N, Ashki M, Montajabi Niat M, Vakili S, Imanian H, Zeinali S, Najmabadi H, Azarkeivan A. Farashi S, et al. Hemoglobin. 2015;39(3):201-6. doi: 10.3109/03630269.2015.1027914. Epub 2015 Jun 18. Hemoglobin. 2015. PMID: 26084319

7

Homozygosity for the AATAAA > AATA- - Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian Patient: A Case Report.

Farashi S, Garous NF, Ashki M, Vakili S, Zeinali F, Imanian H, Azarkeivan A, Giordano PC, Najmabadi H. Farashi S, et al. Hemoglobin. 2015;39(5):355-8. doi: 10.3109/03630269.2015.1059850. Epub 2015 Jul 21. Hemoglobin. 2015. PMID: 26193977

8

Mutations on the α2-Globin Gene That May Trigger α(+)-Thalassemia.

Farashi S, Vakili S, Garous NF, Ashki M, Imanian H, Azarkeivan A, Najmabadi H. Farashi S, et al. Hemoglobin. 2015;39(6):398-402. doi: 10.3109/03630269.2015.1075890. Epub 2015 Sep 2. Hemoglobin. 2015. PMID: 26329872

9

Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes.

Farashi S, Vakili S, Faramarzi Garous N, Ashki M, Imanian H, Azarkeivan A, Najmabadi H. Farashi S, et al. Expert Rev Hematol. 2015 Oct;8(5):693-8. doi: 10.1586/17474086.2015.1075385. Epub 2015 Aug 6. Expert Rev Hematol. 2015. PMID: 26343893 Review.

10

Diagnostic pitfalls of less well recognized HbH disease.

Farashi S, Najmabadi H. Farashi S, et al. Blood Cells Mol Dis. 2015 Dec;55(4):387-95. doi: 10.1016/j.bcmd.2015.08.003. Epub 2015 Aug 8. Blood Cells Mol Dis. 2015. PMID: 26460264 Review.

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