Chaleshtori MH - Search Results

1

Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family.

Reiisi S, Tabatabaiefar MA, Sanati MH, Chaleshtori MH. Reiisi S, et al. Among authors: chaleshtori mh. Iran J Basic Med Sci. 2016 Jul;19(7):772-8. Iran J Basic Med Sci. 2016. PMID: 27635202 Free PMC article.

2

Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran.

Asgharzade S, Reiisi S, Tabatabaiefar MA, Chaleshtori MH. Asgharzade S, et al. Among authors: chaleshtori mh. Iran J Public Health. 2017 Jan;46(1):76-82. Iran J Public Health. 2017. PMID: 28451532 Free PMC article.

3

Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.

Montazer Zohour M, Tabatabaiefar MA, Dehkordi FA, Farrokhi E, Akbari MT, Chaleshtori MH. Montazer Zohour M, et al. Among authors: chaleshtori mh. Genet Test Mol Biomarkers. 2012 Apr;16(4):271-8. doi: 10.1089/gtmb.2011.0176. Epub 2011 Nov 11. Genet Test Mol Biomarkers. 2012. PMID: 22077646

4

Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss.

Yazdanpanahi N, Chaleshtori MH, Tabatabaiefar MA, Noormohammadi Z, Farrokhi E, Najmabadi H, Shahbazi S, Hosseinipour A. Yazdanpanahi N, et al. Among authors: chaleshtori mh. Int J Pediatr Otorhinolaryngol. 2012 Jun;76(6):845-50. doi: 10.1016/j.ijporl.2012.02.056. Epub 2012 Mar 23. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22444735 Free article.

5

Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome.

Yazdanpanahi N, Tabatabaiefar MA, Farrokhi E, Abdian N, Bagheri N, Shahbazi S, Noormohammadi Z, Chaleshtori MH. Yazdanpanahi N, et al. Among authors: chaleshtori mh. Clin Exp Otorhinolaryngol. 2013 Dec;6(4):201-8. doi: 10.3342/ceo.2013.6.4.201. Epub 2013 Nov 29. Clin Exp Otorhinolaryngol. 2013. PMID: 24353858 Free PMC article.

6

A novel TECTA mutation causes ARNSHL.

Asgharzade S, Tabatabaiefar MA, Modarressi MH, Ghahremani MH, Reiisi S, Tahmasebi P, Abdollahnejad F, Chaleshtori MH. Asgharzade S, et al. Among authors: chaleshtori mh. Int J Pediatr Otorhinolaryngol. 2017 Jan;92:88-93. doi: 10.1016/j.ijporl.2016.11.010. Epub 2016 Nov 15. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28012541 Free article.

7

A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing.

Asgharzade S, Tabatabaiefar MA, Mohammadi-Asl J, Chaleshtori MH. Asgharzade S, et al. Among authors: chaleshtori mh. Int J Pediatr Otorhinolaryngol. 2018 May;108:8-11. doi: 10.1016/j.ijporl.2018.01.006. Epub 2018 Jan 31. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29605370

8

Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the CEL Gene.

Sarmadi A, Mohammadi A, Tabatabaei F, Nouri Z, Chaleshtori MH, Tabatabaiefar MA. Sarmadi A, et al. Among authors: chaleshtori mh. Adv Biomed Res. 2020 Jun 27;9:25. doi: 10.4103/abr.abr_18_20. eCollection 2020. Adv Biomed Res. 2020. PMID: 33072637 Free PMC article.

9

A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment.

Schrauwen I, Helfmann S, Inagaki A, Predoehl F, Tabatabaiefar MA, Picher MM, Sommen M, Zazo Seco C, Oostrik J, Kremer H, Dheedene A, Claes C, Fransen E, Chaleshtori MH, Coucke P, Lee A, Moser T, Van Camp G. Schrauwen I, et al. Among authors: chaleshtori mh. Am J Hum Genet. 2012 Oct 5;91(4):636-45. doi: 10.1016/j.ajhg.2012.08.018. Epub 2012 Sep 13. Am J Hum Genet. 2012. PMID: 22981119 Free PMC article.

10

Study of VSX1 mutations in patients with keratoconus in southwest Iran using PCR-single-strand conformation polymorphism/heteroduplex analysis and sequencing method.

Dehkordi FA, Rashki A, Bagheri N, Chaleshtori MH, Memarzadeh E, Salehi A, Ghatreh H, Zandi F, Yazdanpanahi N, Tabatabaiefar MA, Chaleshtori MH. Dehkordi FA, et al. Among authors: chaleshtori mh. Acta Cytol. 2013;57(6):646-51. doi: 10.1159/000353297. Epub 2013 Oct 1. Acta Cytol. 2013. PMID: 24107477

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