Hashemzadeh-Chaleshtori M - Search Results

1

A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family.

Koohiyan M, Noori-Daloii MR, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Tabatabaiefar MA. Koohiyan M, et al. Audiol Neurootol. 2019;24(5):258-263. doi: 10.1159/000502251. Epub 2019 Oct 29. Audiol Neurootol. 2019. PMID: 31661684

2

A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss.

Tabatabaiefar MA, Pourreza MR, Tahmasebi P, Saki N, Hashemzadeh Chaleshtori M, Salehi R, Mohammadi-Asl J. Tabatabaiefar MA, et al. Otolaryngol Head Neck Surg. 2018 Jun;158(6):1084-1092. doi: 10.1177/0194599818759007. Epub 2018 Feb 27. Otolaryngol Head Neck Surg. 2018. PMID: 29484972

3

GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants.

Koohiyan M, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Reiisi S, Pourreza MR, Noori-Daloii MR, Tabatabaiefar MA. Koohiyan M, et al. Int J Pediatr Otorhinolaryngol. 2018 Apr;107:121-126. doi: 10.1016/j.ijporl.2018.01.012. Epub 2018 Jan 31. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29501291

4

A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.

Taghipour-Sheshdeh A, Nemati-Zargaran F, Zarepour N, Tahmasebi P, Saki N, Tabatabaiefar MA, Mohammadi-Asl J, Hashemzadeh-Chaleshtori M. Taghipour-Sheshdeh A, et al. Genomics. 2019 Jul;111(4):840-848. doi: 10.1016/j.ygeno.2018.05.008. Epub 2018 May 9. Genomics. 2019. PMID: 29752989 Free article.

5

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. 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

6

Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss.

Azadegan-Dehkordi F, Ahmadi R, Koohiyan M, Hashemzadeh-Chaleshtori M. Azadegan-Dehkordi F, et al. Ann Hum Genet. 2019 Jan;83(1):1-10. doi: 10.1111/ahg.12284. Epub 2018 Sep 3. Ann Hum Genet. 2019. PMID: 30175840 Review.

7

Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran.

Azadegan-Dehkordi F, Bahrami T, Shirzad M, Karbasi G, Yazdanpanahi N, Farrokhi E, Koohiyan M, Tabatabaiefar MA, Hashemzadeh-Chaleshtori M. Azadegan-Dehkordi F, et al. J Audiol Otol. 2019 Jan;23(1):20-26. doi: 10.7874/jao.2018.00185. Epub 2018 Dec 7. J Audiol Otol. 2019. PMID: 30518198 Free PMC article.

8

Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing.

Zarepour N, Koohiyan M, Taghipour-Sheshdeh A, Nemati-Zargaran F, Saki N, Mohammadi-Asl J, Tabatabaiefar MA, Hashemzadeh-Chaleshtori M. Zarepour N, et al. Audiol Neurootol. 2019;24(1):25-31. doi: 10.1159/000498843. Epub 2019 Apr 3. Audiol Neurootol. 2019. PMID: 30943474

9

Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred.

Sadeghian L, Tabatabaiefar MA, Fattahi N, Pourreza MR, Tahmasebi P, Alavi Z, Hashemzadeh Chaleshtori M. Sadeghian L, et al. Int J Pediatr Otorhinolaryngol. 2019 Sep;124:99-105. doi: 10.1016/j.ijporl.2019.05.023. Epub 2019 May 21. Int J Pediatr Otorhinolaryngol. 2019. PMID: 31176026

10

A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family.

Pourahmadiyan A, Alipour P, Fattahi N, Kasiri M, Rezaeian F, Taghipour-Sheshdeh A, Mohammadi-Asl J, Tabatabaiefar MA, Hashemzadeh Chaleshtori M. Pourahmadiyan A, et al. Int J Audiol. 2019 Oct;58(10):628-634. doi: 10.1080/14992027.2019.1619945. Epub 2019 Jun 12. Int J Audiol. 2019. PMID: 31187663

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