Items where Author is "Fattahi, N."

(2022) Current Inequities in Smoking Prevalence on District Level in Iran: A Systematic Analysis on the STEPS Survey. JOURNAL OF RESEARCH IN HEALTH SCIENCES. ISSN 2228-7795 2228-7809 J9 - J RES HEALTH SCI

(2020) Treatment ofCOVID-19 with pentoxifylline: Could it be a potential adjuvant therapy? Dermatologic Therapy. ISSN 1396-0296

(2019) Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation. JOURNAL OF CELLULAR BIOCHEMISTRY. ISSN 1097-4644 (Electronic) 0730-2312 (Linking)

(2019) Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred. Int J Pediatr Otorhinolaryngol. pp. 99-105. ISSN 1872-8464 (Electronic) 0165-5876 (Linking)

(2019) A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family. Int J Audiol. pp. 1-7. ISSN 1708-8186 (Electronic) 1499-2027 (Linking)

(2017) A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis. Journal of the Neurological Sciences. pp. 212-216. ISSN 0022-510X

(2016) Genetic linkage analysis of DFNB40 and DFNB48 loci in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from western provinces of Iran. Journal of Isfahan Medical School. ISSN 10277595 (ISSN)

(2015) Genetic linkage analysis of the DFNB63 locus in families with autosomal recessive nonsyndromic hearing loss from Hamadan and Kohgiluyeh and Boyer-Ahmad Provinces, Iran. Journal of Isfahan Medical School. pp. 1308-1317. ISSN 10277595 (ISSN)