Items where Author is "Hashemzadeh-Chaleshtori, M."

Article

(2021) Molecular diagnosis of SLC26A4-related hereditary hearing loss in a group of patients from two provinces of Iran. Intractable & Rare Diseases Research. pp. 23-30. ISSN 2186-3644

(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

(2019) Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations. Journal of Audiology and Otology. pp. 175-180. ISSN 2384-1621

(2019) Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations. Intractable & Rare Diseases Research. pp. 172-178. ISSN 2186-3644

(2019) Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing. Audiology and Neuro-Otology. pp. 25-31. ISSN 1420-3030

(2019) Mutation Analysis of GJB2 and GJB6 Genes and Screening of Nine Common DFNB Loci in Iranian Pedigrees with Autosomal Recessive Nonsyndromic Hearing Loss. Indian Journal of Otology. pp. 97-102. ISSN 0971-7749

(2019) 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. Journal of Audiology and Otology. pp. 20-26. ISSN 2384-1621

(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) A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Genomics. pp. 840-848. ISSN 0888-7543

(2019) An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review. International Journal of Pediatric Otorhinolaryngology. pp. 136-140. ISSN 0165-5876

(2018) Clinical Aspects of Microsatellite Instability Testing in Colorectal Cancer. Adv Biomed Res. p. 28. ISSN 2277-9175 (Print) 2277-9175 (Linking)

(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

(2018) A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Genomics. ISSN 1089-8646 (Electronic) 0888-7543 (Linking)

(2018) A novel variant of SLC26A4 and first report of the c.716T > A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss. American Journal of Otolaryngology. pp. 719-725. ISSN 0196-0709

(2017) GENOTYPING OF Trichomonas vaginalis ISOLATES FROM WOMEN IN SHAHREKORD CITY (SOUTHWESTERN IRAN). Genetika-Belgrade. pp. 1059-1070. ISSN 0534-0012

(2017) The Lack of Correlation between Tp53 Mutations and Gastric Cancer: A Report from a Province of Iran. Genetika-Belgrade. pp. 235-246. ISSN 0534-0012

(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) Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis. Jundishapur Journal of Microbiology. ISSN 2008-3645

(2015) Epidemioclinical feature of early-onset colorectal cancer at-risk for lynch syndrome in Central Iran. Asian Pacific Journal of Cancer Prevention. pp. 4647-4652. ISSN 15137368 (ISSN)

(2015) Frequency of virulence factors in Helicobacter pylori-infected patients with gastritis. Microbial Pathogenesis. pp. 67-72. ISSN 0882-4010

(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)

(2015) Genotyping of Trichomonas vaginalis in symptomatic women in Shahrekord city (southwestern Iran), 2011. Genetic Epidemiology. p. 551. ISSN 0741-0395

(2015) Immunohistochemical analysis of mismatch repair proteins in Iranian Colorectal Cancer patients at risk for Lynch syndrome. Iranian Journal of Cancer Prevention. pp. 11-17. ISSN 2008-2398

(2015) Molecular Analysis of Iranian Colorectal Cancer Patients at Risk for Lynch Syndrome: a New Molecular, Clinicopathological Feature. Journal of Gastrointestinal Cancer. pp. 118-125. ISSN 19416628 (ISSN)

(2015) Screening BRCA1 and BRCA2 Mutation Frequencies In Breast Cancer Patients Of West Iran Reveals a Novel Polymorphism In BRCA1 Gene. European Journal of Oncology. pp. 94-99. ISSN 11286598 (ISSN)

(2015) Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome. Journal of Research in Medical Sciences. pp. 154-160. ISSN 1735-1995