Najmabadi H - Search Results

1

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. Among authors: najmabadi h. Hemoglobin. 2015;39(3):196-200. doi: 10.3109/03630269.2015.1030757. Epub 2015 May 15. Hemoglobin. 2015. PMID: 25976776

2

The beta-thalassemia mutation spectrum in the Iranian population.

Najmabadi H, Karimi-Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, Amirizadeh N, Karimi-Nejad MH. Najmabadi H, et al. Hemoglobin. 2001 Aug;25(3):285-96. doi: 10.1081/hem-100105221. Hemoglobin. 2001. PMID: 11570721

3

High prevalence of the -alpha3.7 deletion among thalassemia patients in Iran.

Neishabury M, Oberkanins C, Moheb LA, Pourfatholuah AA, Kahrizi K, Keyhany E, Krugluger W, Najmabadi H. Neishabury M, et al. Among authors: najmabadi h. Hemoglobin. 2003 Feb;27(1):53-5. doi: 10.1081/hem-120018438. Hemoglobin. 2003. PMID: 12603096 No abstract available.

4

Hb Dhonburi (Neapolis) [beta126(H4)Val-->Gly] identified in a family from northern Iran.

Moghimi B, Yavarian M, Oberkanins C, Amini SS, Khatami S, Rouhi S, Kahrizi K, Najmabadi H. Moghimi B, et al. Among authors: najmabadi h. Hemoglobin. 2004;28(4):353-6. doi: 10.1081/hem-200038876. Hemoglobin. 2004. PMID: 15658193

5

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: najmabadi h. Haematologica. 2007 Jul;92(7):992-3. doi: 10.3324/haematol.10658. Haematologica. 2007. PMID: 17606454 Free article.

6

Globin chain synthesis is a useful complementary tool in the differential diagnosis of thalassemias.

Khatami S, Dehboneh SR, Sadeghi S, Mirzazadeh R, Saeedi P, Bayat P, Najmabadi H, Zeinali S, Akbari MT, Ardjmand M, Amirkhani A. Khatami S, et al. Among authors: najmabadi h. Hemoglobin. 2007;31(3):333-41. doi: 10.1080/03630260701462006. Hemoglobin. 2007. PMID: 17654070

7

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

8

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: najmabadi h. Genet Test. 2008 Dec;12(4):549-56. doi: 10.1089/gte.2008.0018. Genet Test. 2008. PMID: 18939939

9

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

10

Molecular characterization of alpha-thalassemia in the Dohuk region of Iraq.

Al-Allawi NA, Badi AI, Imanian H, Nikzat N, Jubrael JM, Najmabadi H. Al-Allawi NA, et al. Among authors: najmabadi h. Hemoglobin. 2009;33(1):37-44. doi: 10.1080/03630260802626053. Hemoglobin. 2009. PMID: 19205971

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