Imanian H - Search Results

1

Gene Panel Testing in Hereditary Breast Cancer.

Rostami P, Zendehdel K, Shirkoohi R, Ebrahimi E, Ataei M, Imanian H, Najmabadi H, Akbari MR, Sanati MH. Rostami P, et al. Among authors: imanian h. Arch Iran Med. 2020 Mar 1;23(3):155-162. Arch Iran Med. 2020. PMID: 32126783

2

Prenatal Screening for Aneuploidies Using QF-PCR and Karyotyping: A Comprehensive Study in Iranian Population.

Rostami P, Valizadegan S, Ghalandary M, Mehrjouy MM, Esmail-Nia G, Khalili S, Shahmoradi SS, Imanian H, Hadavi V, Ghaderi-Sohi S, Almadani N, Afroozan F, Kariminejad A, Kariminejad R, Najmabadi H. Rostami P, et al. Among authors: imanian h. Arch Iran Med. 2015 May;18(5):296-303. Arch Iran Med. 2015. PMID: 25959911

3

Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.

Esteghamat F, Imanian H, Azarkeivan A, Pourfarzad F, Almadani N, Najmabadi H. Esteghamat F, et al. Among authors: imanian h. Hemoglobin. 2007;31(4):463-9. doi: 10.1080/03630260701641286. Hemoglobin. 2007. PMID: 17994380

4

Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population.

Farashi S, Garous NF, Vakili S, Ashki M, Imanian H, Azarkeivan A, Najmabadi H. Farashi S, et al. Among authors: imanian h. Hemoglobin. 2016;40(1):53-5. doi: 10.3109/03630269.2015.1091357. Epub 2015 Nov 16. Hemoglobin. 2016. PMID: 26574177

5

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. Among authors: imanian h. Hemoglobin. 2015;39(6):398-402. doi: 10.3109/03630269.2015.1075890. Epub 2015 Sep 2. Hemoglobin. 2015. PMID: 26329872

6

Genotype-phenotype correlation in Iranian patients with Hb H disease.

Ebrahimkhani S, Azarkeivan A, Bayat N, Houry-Parvin M, Jalil-Nejad S, Zand S, Golkar Z, Hadavi V, Imanian H, Oberkanins C, Najmabadi H. Ebrahimkhani S, et al. Among authors: imanian h. Hemoglobin. 2011;35(1):40-6. doi: 10.3109/03630269.2010.546314. Hemoglobin. 2011. PMID: 21250880

7

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: imanian h. Hemoglobin. 2013;37(2):148-59. doi: 10.3109/03630269.2013.763821. Epub 2013 Feb 12. Hemoglobin. 2013. PMID: 23402770

8

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. Among authors: imanian h. Hemoglobin. 2015;39(3):152-5. doi: 10.3109/03630269.2015.1027915. Epub 2015 May 15. Hemoglobin. 2015. PMID: 25976777

9

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. Among authors: imanian h. Hemoglobin. 2015;39(3):201-6. doi: 10.3109/03630269.2015.1027914. Epub 2015 Jun 18. Hemoglobin. 2015. PMID: 26084319

10

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. Among authors: imanian h. 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.

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