Farrokhi E - Search Results

1

DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment.

Tabatabaiefar MA, Alasti F, Shariati L, Farrokhi E, Fransen E, Nooridaloii MR, Chaleshtori MH, Van Camp G. Tabatabaiefar MA, et al. Among authors: farrokhi e. Clin Genet. 2011 Jun;79(6):594-8. doi: 10.1111/j.1399-0004.2010.01593.x. Clin Genet. 2011. PMID: 21542834 No abstract available.

2

Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families.

Hashemzadeh Chaleshtori M, Simpson MA, Farrokhi E, Dolati M, Hoghooghi Rad L, Amani Geshnigani S, Crosby AH. Hashemzadeh Chaleshtori M, et al. Among authors: farrokhi e. Clin Genet. 2007 Sep;72(3):261-3. doi: 10.1111/j.1399-0004.2007.00852.x. Clin Genet. 2007. PMID: 17718865 No abstract available.

3

A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame.

Vanwesemael M, Schrauwen I, Ceuppens R, Alasti F, Jorssen E, Farrokhi E, Chaleshtori MH, Van Camp G. Vanwesemael M, et al. Among authors: farrokhi e. Am J Med Genet A. 2011 Aug;155A(8):2021-3. doi: 10.1002/ajmg.a.34096. Epub 2011 Jul 7. Am J Med Genet A. 2011. PMID: 21739586 No abstract available.

4

Increased levels of miR-124 in human dental pulp stem cells alter the expression of neural markers.

Mehri-Ghahfarrokhi A, Pourteymourfard-Tabrizi Z, Farrokhi E, Chaleshtori MH, Jami MS. Mehri-Ghahfarrokhi A, et al. Among authors: farrokhi e. J Otol. 2019 Dec;14(4):121-127. doi: 10.1016/j.joto.2019.04.001. Epub 2019 Apr 16. J Otol. 2019. PMID: 32742271 Free PMC article.

5

Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: assessment of GJB4, GJA1, and GJC3.

Kooshavar D, Tabatabaiefar MA, Farrokhi E, Abolhasani M, Noori-Daloii MR, Hashemzadeh-Chaleshtori M. Kooshavar D, et al. Among authors: farrokhi e. Int J Pediatr Otorhinolaryngol. 2013 Feb;77(2):189-93. doi: 10.1016/j.ijporl.2012.10.015. Epub 2012 Nov 8. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23141803

6

The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness.

Yazdanpanahi N, Tabatabaiefar MA, Bagheri N, Azadegan Dehkordi F, Farrokhi E, Hashemzadeh Chaleshtori M. Yazdanpanahi N, et al. Among authors: farrokhi e. Int J Audiol. 2015 Feb;54(2):124-30. doi: 10.3109/14992027.2014.944276. Epub 2014 Oct 7. Int J Audiol. 2015. PMID: 25290043

7

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: farrokhi e. 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

8

A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss.

Azadegan-Dehkordi F, Ahmadi R, Bahrami T, Yazdanpanahi N, Farrokhi E, Tabatabaiefar MA, Hashemzadeh-Chaleshtori M. Azadegan-Dehkordi F, et al. Among authors: farrokhi e. Am J Otolaryngol. 2018 Nov-Dec;39(6):719-725. doi: 10.1016/j.amjoto.2018.07.022. Epub 2018 Jul 27. Am J Otolaryngol. 2018. PMID: 30077349

9

Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss.

Tabatabaiefar M, Alasti F, Zohour MM, Shariati L, Farrokhi E, Farhud D, Camp G, Noori-Daloii M, Chaleshtori MH. Tabatabaiefar M, et al. Among authors: farrokhi e. Iran J Public Health. 2011;40(2):34-48. Epub 2011 Jun 30. Iran J Public Health. 2011. PMID: 23113071 Free PMC article.

10

High carrier frequency of the GJB2 mutation (35delG) in the north of Iran.

Chaleshtori MH, Farrokhi E, Shahrani M, Kheiri S, Dolati M, Rad LH, Pour-Jafari H, Samani KG, Chaleshtori KS, Crosby AH. Chaleshtori MH, et al. Among authors: farrokhi e. Int J Pediatr Otorhinolaryngol. 2007 Jun;71(6):863-7. doi: 10.1016/j.ijporl.2007.02.005. Epub 2007 Apr 10. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17428550

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