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Items: 10

1.

Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations.

Koohiyan M, Azadegan-Dehkordi F, Koohian F, Abolhasani M, Hashemzadeh-Chaleshtori M.

Intractable Rare Dis Res. 2019 Aug;8(3):172-178. doi: 10.5582/irdr.2019.01070. Review.

2.

GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations.

Koohiyan M, Koohian F, Azadegan-Dehkordi F.

Ann Hum Genet. 2019 Sep 11. doi: 10.1111/ahg.12354. [Epub ahead of print] Review.

PMID:
31512227
3.

Genetics of Hereditary Hearing Loss in the Middle East: A Systematic Review of the Carrier Frequency of the GJB2 Mutation (35delG).

Koohiyan M.

Audiol Neurootol. 2019 Sep 5:1-5. doi: 10.1159/000502201. [Epub ahead of print]

PMID:
31487726
4.

A Systematic Review of the Genotoxicity and Antigenotoxicity of Biologically Synthesized Metallic Nanomaterials: Are Green Nanoparticles Safe Enough for Clinical Marketing?

Barabadi H, Najafi M, Samadian H, Azarnezhad A, Vahidi H, Mahjoub MA, Koohiyan M, Ahmadi A.

Medicina (Kaunas). 2019 Aug 5;55(8). pii: E439. doi: 10.3390/medicina55080439. Review.

5.

A systematic review of SLC26A4 mutations causing hearing loss in the Iranian population.

Koohiyan M.

Int J Pediatr Otorhinolaryngol. 2019 Oct;125:1-5. doi: 10.1016/j.ijporl.2019.06.012. Epub 2019 Jun 14. Review.

PMID:
31228605
6.

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.

Audiol Neurootol. 2019;24(1):25-31. doi: 10.1159/000498843. Epub 2019 Apr 3.

PMID:
30943474
7.

An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review.

Koohiyan M, Ahmadi A, Koohian F, Aghaei S, Amiri B, Hashemzadeh-Chaleshtori M.

Int J Pediatr Otorhinolaryngol. 2019 Apr;119:136-140. doi: 10.1016/j.ijporl.2019.01.036. Epub 2019 Jan 25. Review.

PMID:
30708180
8.

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.

J Audiol Otol. 2019 Jan;23(1):20-26. doi: 10.7874/jao.2018.00185. Epub 2018 Dec 7.

9.

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.

Ann Hum Genet. 2019 Jan;83(1):1-10. doi: 10.1111/ahg.12284. Epub 2018 Sep 3. Review.

PMID:
30175840
10.

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.

Int J Pediatr Otorhinolaryngol. 2018 Apr;107:121-126. doi: 10.1016/j.ijporl.2018.01.012. Epub 2018 Jan 31.

PMID:
29501291

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