Zeinali S - Search Results

1

Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling.

Mahdieh N, Shirkavand A, Raeisi M, Akbari MT, Tekin M, Zeinali S. Mahdieh N, et al. Among authors: zeinali s. Biochem Biophys Res Commun. 2010 Nov 12;402(2):305-7. doi: 10.1016/j.bbrc.2010.10.021. Epub 2010 Oct 19. Biochem Biophys Res Commun. 2010. PMID: 20937258

2

A novel single step double positive double negative selection strategy for beta-globin gene replacement.

Khanahmad H, Noori Daloii MR, Shokrgozar MA, Azadmanesh K, Niavarani AR, Karimi M, Rabbani B, Khalili M, Bagheri R, Maryami F, Zeinali S. Khanahmad H, et al. Among authors: zeinali s. Biochem Biophys Res Commun. 2006 Jun 23;345(1):14-20. doi: 10.1016/j.bbrc.2006.04.060. Epub 2006 Apr 25. Biochem Biophys Res Commun. 2006. PMID: 16674923

3

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: zeinali s. J Pediatr Hematol Oncol. 2007 Apr;29(4):233-8. doi: 10.1097/MPH.0b013e3180437e02. J Pediatr Hematol Oncol. 2007. PMID: 17414565

4

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: zeinali s. Hemoglobin. 2007;31(3):333-41. doi: 10.1080/03630260701462006. Hemoglobin. 2007. PMID: 17654070

5

Characterization of minor bands of STR amplification reaction of FVIII gene by PCR cloning.

Rabbani B, Khanahmad H, Bagheri R, Mahdieh N, Zeinali S. Rabbani B, et al. Among authors: zeinali s. Clin Chim Acta. 2008 Aug;394(1-2):114-5. doi: 10.1016/j.cca.2008.03.003. Epub 2008 Mar 18. Clin Chim Acta. 2008. PMID: 18402778 No abstract available.

6

Detection of unknown deletions in beta-globin gene cluster using relative quantitative PCR methods.

Babashah S, Jamali S, Mahdian R, Nosaeid MH, Karimipoor M, Alimohammadi R, Raeisi M, Maryami F, Masoudifar M, Zeinali S. Babashah S, et al. Among authors: zeinali s. Eur J Haematol. 2009 Sep;83(3):261-9. doi: 10.1111/j.1600-0609.2009.01264.x. Epub 2009 Apr 1. Eur J Haematol. 2009. PMID: 19341428

7

The Cretan type of nondeletional hereditary persistence of fetal hemoglobin in an Iranian family.

Hamid M, Mahjoubi F, Akbari MT, Zeinali S, Karimipoor M. Hamid M, et al. Among authors: zeinali s. Ann Hematol. 2009 Dec;88(12):1267-8. doi: 10.1007/s00277-009-0756-0. Epub 2009 May 26. Ann Hematol. 2009. PMID: 19468729 No abstract available.

8

Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia.

Fallah MS, Zadeh-Vakili A, Aleyasin SA, Mahdian R, Karimipour M, Raeisi M, Jamali S, Ebrahimi A, Fooladi P, Naderi M, Baysal E, Zeinali S. Fallah MS, et al. Among authors: zeinali s. Blood Cells Mol Dis. 2009 Sep-Oct;43(2):158-60. doi: 10.1016/j.bcmd.2009.05.006. Epub 2009 Jul 3. Blood Cells Mol Dis. 2009. PMID: 19577494 No abstract available.

9

Molecular analysis of gamma-globin promoters, HS-111 and 3'HS1, in beta-thalassemia intermedia patients associated with high levels of Hb F.

Hamid M, Mahjoubi F, Akbari MT, Arab A, Zeinali S, Karimipoor M. Hamid M, et al. Among authors: zeinali s. Hemoglobin. 2009;33(6):428-38. doi: 10.3109/03630260903336479. Hemoglobin. 2009. PMID: 19958188

10

Development of a quantitative real-time PCR assay for detection of unknown alpha-globin gene deletions.

Fallah MS, Mahdian R, Aleyasin SA, Jamali S, Hayat-Nosaeid M, Karimipour M, Raeisi M, Zeinali S. Fallah MS, et al. Among authors: zeinali s. Blood Cells Mol Dis. 2010 Jun 15;45(1):58-64. doi: 10.1016/j.bcmd.2010.03.001. Epub 2010 Apr 2. Blood Cells Mol Dis. 2010. PMID: 20363165

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