Lista de obras - Suna Tokgöz Yilmaz - Dominio Público Uruguay

A Novel Variant in SYNE4 Confirms its Causative Role in Sensorineural Hearing Loss.

artículo científico publicado en 2017

A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss

artículo científico publicado en 2019

Audiological findings in Noonan syndrome.

artículo científico publicado en 2016

Audiological findings in otospondylomegaepiphyseal dysplasia (OSMED) associated with a novel mutation in COL11A2.

artículo científico publicado en 2011

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

artículo científico publicado en 2015

Does glutaric aciduria type 1 affect hearing function?

artículo científico publicado en 2022

Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss

scientific article published on 04 January 2019

Effects of GJB2 genotypes on the audiological phenotype: variability is present for all genotypes

artículo científico publicado en 2006

Evaluation of Speech Recognition Skills in Different Noises with the Turkish Matrix Sentence Test in Hearing Aid Users

artículo científico publicado en 2021

Evidence for genotype-phenotype correlation for OTOF mutations

artículo científico publicado en 2014

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing.

artículo científico publicado en 2014

Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.

artículo científico publicado en 2012

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations.

artículo científico publicado en 2009

Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss

scientific article published on 27 August 2019

ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.

artículo científico publicado en 2016

Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.

artículo científico publicado en 2010

SLITRK6 mutations cause myopia and deafness in humans and mice

artículo científico publicado en 2013

The role of the medial olivocochlear system in the complaints of understanding speech in noisy environments by individuals with normal hearing.

artículo científico publicado en 2013

Transcutaneous Electric Nerve Stimulation in Chronic Subjective Tinnitus

artículo científico publicado en 2022

Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss

artículo científico publicado en 2016

Lista de obras de Suna Tokgöz Yilmaz

A Novel Variant in SYNE4 Confirms its Causative Role in Sensorineural Hearing Loss.

A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss

Audiological findings in Noonan syndrome.

Audiological findings in otospondylomegaepiphyseal dysplasia (OSMED) associated with a novel mutation in COL11A2.

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Does glutaric aciduria type 1 affect hearing function?

Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss

Effects of GJB2 genotypes on the audiological phenotype: variability is present for all genotypes

Evaluation of Speech Recognition Skills in Different Noises with the Turkish Matrix Sentence Test in Hearing Aid Users

Evidence for genotype-phenotype correlation for OTOF mutations

FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing.

Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations.

Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing loss

ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.

Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.

SLITRK6 mutations cause myopia and deafness in humans and mice

The role of the medial olivocochlear system in the complaints of understanding speech in noisy environments by individuals with normal hearing.

Transcutaneous Electric Nerve Stimulation in Chronic Subjective Tinnitus

Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss