Najmabadi H - Search Results

1

Pattern of immunoglobulin and T-cell receptor-δ/γ gene rearrangements in Iranian children with B-precursor acute lymphoblastic leukemia.

Poopak B, Saki N, Purfatholah AA, Najmabadi H, Mortazavi Y, Arzanian MT, Khosravipour G, Haghnejad F, Salari F, Shahjahani M. Poopak B, et al. Among authors: najmabadi h. Hematology. 2014 Jul;19(5):259-66. doi: 10.1179/1607845413Y.0000000126. Epub 2014 Jan 3. Hematology. 2014. PMID: 24620952

2

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: najmabadi h. Hemoglobin. 2018 Jul;42(4):252-256. doi: 10.1080/03630269.2018.1526192. Epub 2018 Nov 19. Hemoglobin. 2018. PMID: 30451045

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: najmabadi h. Hemoglobin. 2007;31(4):463-9. doi: 10.1080/03630260701641286. Hemoglobin. 2007. PMID: 17994380

4

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: najmabadi h. Hemoglobin. 2008;32(6):546-52. doi: 10.1080/03630260802532780. Hemoglobin. 2008. PMID: 19065332

5

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: najmabadi h. 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

6

Analyzing 5'HS3 and 5'HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations.

Neishabury M, Azarkeivan A, Oberkanins C, Abedini SS, Zamani S, Najmabadi H. Neishabury M, et al. Among authors: najmabadi h. Blood Cells Mol Dis. 2011 Mar 15;46(3):201-5. doi: 10.1016/j.bcmd.2010.12.007. Epub 2011 Jan 12. Blood Cells Mol Dis. 2011. PMID: 21232998

7

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: najmabadi h. Hemoglobin. 2011;35(1):40-6. doi: 10.3109/03630269.2010.546314. Hemoglobin. 2011. PMID: 21250880

8

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: najmabadi h. Hemoglobin. 2012;36(4):371-80. doi: 10.3109/03630269.2012.691147. Epub 2012 Jun 11. Hemoglobin. 2012. PMID: 22686296

9

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

10

Utility of the multivariate approach in predicting β-thalassemia intermedia or β-thalassemia major types In Iranian patients.

Banan M, Bayat H, Namdar-Aligoodarzi P, Azarkeivan A, Kamali K, Daneshmand P, Zaker-Kandjani B, Najmabadi H. Banan M, et al. Among authors: najmabadi h. Hemoglobin. 2013;37(5):413-22. doi: 10.3109/03630269.2013.805418. Epub 2013 Jun 27. Hemoglobin. 2013. PMID: 23805990

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