Mahdieh N - Search Results

1

A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect.

Davoudi-Dehaghani E, Zeinali S, Mahdieh N, Shirkavand A, Bagherian H, Tabatabaiefar MA. Davoudi-Dehaghani E, et al. Among authors: mahdieh n. Int J Pediatr Otorhinolaryngol. 2013 May;77(5):821-6. doi: 10.1016/j.ijporl.2013.02.021. Epub 2013 Mar 21. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23523375

2

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: mahdieh n. 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.

3

High level of intrafamilial phenotypic variability of non-syndromic hearing loss in a Lur family due to delE120 mutation in GJB2 gene.

Mahdieh N, Bagherian H, Shirkavand A, Sharafi M, Zeinali S. Mahdieh N, et al. Int J Pediatr Otorhinolaryngol. 2010 Sep;74(9):1089-91. doi: 10.1016/j.ijporl.2010.06.005. Epub 2010 Jul 6. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20609484

4

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations.

Mahdieh N, Rabbani B, Wiley S, Akbari MT, Zeinali S. Mahdieh N, et al. J Hum Genet. 2010 Oct;55(10):639-48. doi: 10.1038/jhg.2010.96. Epub 2010 Aug 26. J Hum Genet. 2010. PMID: 20739942 Review.

5

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. 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

6

Investigation of GJB6 large deletions in Iranian patients using quantitative real-time PCR.

Mahdieh N, Raeisi M, Shirkavand A, Bagherian H, Akbari MT, Zeinali S. Mahdieh N, et al. Clin Lab. 2010;56(9-10):467-71. Clin Lab. 2010. PMID: 21086793

7

Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variant.

Mahdieh N, Rabbani B, Shirkavand A, Bagherian H, Movahed ZS, Fouladi P, Rahiminejad F, Masoudifard M, Akbari MT, Zeinali S. Mahdieh N, et al. Genet Test Mol Biomarkers. 2011 Jul-Aug;15(7-8):489-93. doi: 10.1089/gtmb.2010.0145. Epub 2011 Mar 9. Genet Test Mol Biomarkers. 2011. PMID: 21388256

8

Screening of OTOF mutations in Iran: a novel mutation and review.

Mahdieh N, Shirkavand A, Rabbani B, Tekin M, Akbari B, Akbari MT, Zeinali S. Mahdieh N, et al. Int J Pediatr Otorhinolaryngol. 2012 Nov;76(11):1610-5. doi: 10.1016/j.ijporl.2012.07.030. Epub 2012 Aug 18. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22906306

9

Design of a biological method for rapid detection of presence of PCR inhibitors in aged bone DNA.

Ghasemi A, Mahdieh N, Tavallaei M, Aslani MM, Zafari Z, Shirkavand A, Farzad MS, Naderi M, Azariyan SH, Zeinali S. Ghasemi A, et al. Among authors: mahdieh n. Clin Lab. 2012;58(7-8):681-6. Clin Lab. 2012. PMID: 22997968

10

A novel PCBD gene mutation in an Iranian patient with hyperphenylalaninemia.

Raeisi M, Mahdieh N, Yousefzadeh A, Vahidi R, Rahimi N, Zeinali S. Raeisi M, et al. Among authors: mahdieh n. Clin Lab. 2013;59(7-8):925-8. doi: 10.7754/clin.lab.2013.121017. Clin Lab. 2013. PMID: 24133926 Free article.

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