Neishabury M - Search Results

1

The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5'HS4.

Neishabury M, Zamani S, Azarkeivan A, Abedini SS, Darvish H, Zamani F, Najmabadi H. Neishabury M, et al. Blood Cells Mol Dis. 2012 Jan 15;48(1):1-5. doi: 10.1016/j.bcmd.2011.10.001. Epub 2011 Oct 28. Blood Cells Mol Dis. 2012. PMID: 22036762

2

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. Among authors: neishabury m. Haematologica. 2002 Oct;87(10):1113-4. Haematologica. 2002. PMID: 12368169 No abstract available.

3

The Iranian Human Mutation Gene Bank: a data and sample resource for worldwide collaborative genetics research.

Najmabadi H, Neishabury M, Sahebjam F, Kahrizi K, Shafaghati Y, Nikzat N, Jalalvand M, Aminy F, Hashemi SB, Moghimi B, Noorian AR, Jannati A, Mohammadi M, Javan K; Iranian Human Mutation Gene Bank. Najmabadi H, et al. Among authors: neishabury m. Hum Mutat. 2003 Feb;21(2):146-50. doi: 10.1002/humu.10164. Hum Mutat. 2003. PMID: 12552562

4

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. Hemoglobin. 2003 Feb;27(1):53-5. doi: 10.1081/hem-120018438. Hemoglobin. 2003. PMID: 12603096 No abstract available.

5

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: neishabury m. Haematologica. 2003 Oct;88(10):1196-7. Haematologica. 2003. PMID: 14555321 Review.

6

Molecular mechanisms underlying thalassemia intermedia in Iran.

Neishabury M, Azarkeivan A, Oberkanins C, Esteghamat F, Amirizadeh N, Najmabadi H. Neishabury M, et al. Genet Test. 2008 Dec;12(4):549-56. doi: 10.1089/gte.2008.0018. Genet Test. 2008. PMID: 18939939

7

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. 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

8

A report of 8 cases with hemoglobin H disease in an Iranian family.

Azarkeivan A, Neishabury M, Hadavi V, Esteghamat F, Enrahimkhani S, Najmabadi H. Azarkeivan A, et al. Among authors: neishabury m. Pediatr Hematol Oncol. 2010 Aug;27(5):405-12. doi: 10.3109/08880010903536201. Pediatr Hematol Oncol. 2010. PMID: 20670167

9

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. 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

10

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

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