Najmabadi H - Search Results

1

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

2

Identification of a novel beta0-thalassemia mutation, codons 80/81 (-C), in an Iranian family.

Feleki X, Najmabadi H, Karimi-Nejad R, Christopoulos G, Kleanthous M. Feleki X, et al. Among authors: najmabadi h. Hemoglobin. 2000 Nov;24(4):319-21. doi: 10.3109/03630260008993139. Hemoglobin. 2000. PMID: 11186262 No abstract available.

3

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

4

Rare and unexpected mutations among Iranian beta-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing.

Najmabadi H, Pourfathollah AA, Neishabury M, Sahebjam F, Krugluger W, Oberkanins C. Najmabadi H, et al. Haematologica. 2002 Oct;87(10):1113-4. Haematologica. 2002. PMID: 12368169 No abstract available.

5

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.

6

alpha-globin gene deletion and point mutation analysis among in Iranian patients with microcytic hypochromic anemia.

Garshasbi M, Oberkanins C, Law HY, Neishabury M, Kariminejad R, Najmabadi H. Garshasbi M, et al. Among authors: najmabadi h. Haematologica. 2003 Oct;88(10):1196-7. Haematologica. 2003. PMID: 14555321 Review.

7

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

8

Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events.

Law HY, Luo HY, Wang W, Ho JF, Najmabadi H, Ng IS, Steinberg MH, Chui DH, Chong SS. Law HY, et al. Among authors: najmabadi h. Haematologica. 2006 Mar;91(3):297-302. Epub 2006 Feb 17. Haematologica. 2006. PMID: 16503550

9

Fourteen-year experience of prenatal diagnosis of thalassemia in Iran.

Najmabadi H, Ghamari A, Sahebjam F, Kariminejad R, Hadavi V, Khatibi T, Samavat A, Mehdipour E, Modell B, Kariminejad MH. Najmabadi H, et al. Community Genet. 2006;9(2):93-7. doi: 10.1159/000091486. Community Genet. 2006. PMID: 16612059

10

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.

Najmabadi H, Motazacker MM, Garshasbi M, Kahrizi K, Tzschach A, Chen W, Behjati F, Hadavi V, Nieh SE, Abedini SS, Vazifehmand R, Firouzabadi SG, Jamali P, Falah M, Seifati SM, Grüters A, Lenzner S, Jensen LR, Rüschendorf F, Kuss AW, Ropers HH. Najmabadi H, et al. Hum Genet. 2007 Mar;121(1):43-8. doi: 10.1007/s00439-006-0292-0. Epub 2006 Nov 21. Hum Genet. 2007. PMID: 17120046

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