Najmabadi H - Search Results

1

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

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

Thalassemia in Iran: epidemiology, prevention, and management.

Abolghasemi H, Amid A, Zeinali S, Radfar MH, Eshghi P, Rahiminejad MS, Ehsani MA, Najmabadi H, Akbari MT, Afrasiabi A, Akhavan-Niaki H, Hoorfar H. Abolghasemi H, et al. Among authors: najmabadi h. J Pediatr Hematol Oncol. 2007 Apr;29(4):233-8. doi: 10.1097/MPH.0b013e3180437e02. J Pediatr Hematol Oncol. 2007. PMID: 17414565

6

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

7

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

8

Prenatal diagnosis for beta-thalassemia major in the Iranian Province of Hormozgan.

Nikuei P, Hadavi V, Rajaei M, Saberi M, Hajizade F, Najmabadi H. Nikuei P, et al. Among authors: najmabadi h. Hemoglobin. 2008;32(6):539-45. doi: 10.1080/03630260802508327. Hemoglobin. 2008. PMID: 19065331

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

alpha-Thalassemia mutation analyses in Mazandaran province, North Iran.

Tamaddoni A, Hadavi V, Nejad NH, Khosh-Ain A, Siami R, Aghai-Meibodi J, Almadani N, Oberkanins C, Law HY, Najmabadi H. Tamaddoni A, et al. Among authors: najmabadi h. Hemoglobin. 2009;33(2):115-23. doi: 10.1080/03630260902817297. Hemoglobin. 2009. PMID: 19373587

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