Items where Author is "Abtahi, Hamidreza"

(2020) A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23. Audiology and Neuro-Otology. pp. 258-262. ISSN 1420-3030

(2020) Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss. Molecular Biology Reports. pp. 5355-5364. ISSN 0301-4851

(2020) A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Bmc Medical Genetics.

(2019) Molecular epidemiology of otomycosis in Isfahan revealed a large diversity in causative agents. Journal of Medical Microbiology. pp. 918-923. ISSN 1473-5644 (Electronic) 0022-2615 (Linking)

(2019) A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family. Audiology and Neuro-Otology. pp. 258-263. ISSN 1420-3030

(2019) Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations. Iranian Journal of Public Health. pp. 1704-1713. ISSN 2251-6085

(2019) Therapeutic effect of intratympanic injection of dexamethasone plus hyaluronic acid on patients with meniere's disease. Iranian Journal of Otorhinolaryngology. ISSN 22517251 (ISSN)

(2018) Effect of transcranial direct current stimulation on short-term and long-term treatment of chronic tinnitus. American Journal of Otolaryngology. pp. 94-96. ISSN 0196-0709

(2018) GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants. International Journal of Pediatric Otorhinolaryngology. pp. 121-126. ISSN 0165-5876