Results 71 to 80 of about 75,481 (297)
Hearing and communication self-efficacy in adult hearing aid users and non-users with acquired sensorineural hearing loss [PDF]
, 2015 The purpose of this research study is to determine if differences in hearing and communication self-efficacy exist between adult hearing aid users and non-hearing aid users with acquired sensorineural hearing loss.
Hunt, Ali Christina Mercedes
core +1 more source
Risk factors for sensorineural hearing loss among high-risk infants in Golestan province, Iran in 2010 - 2011 [PDF]
, 2015 Background: Hearing impairment, as one of the most common birth defects, is a hidden disability with negative impacts on speech and cognitive development. Objectives: The aim of this study was to assess the prevalence of sensorineural hearing loss (SNHL)
Alaee, E. +3 more
core +2 more sources
Expanding the Phenotype of TUFM‐Related Combined Oxidative Phosphorylation Deficiency 4
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Combined oxidative phosphorylation deficiency 4 (COXPD4) is a rare mitochondrial condition caused by biallelic deleterious variants in the nuclear‐encoded gene TUFM. To date, most individuals with COXPD4 have presented with encephalopathy, hypotonia, and abnormal brain imaging. Many of the reported individuals died in infancy. We aim to expand
Noémie Villeneuve‐Cloutier +2 more
wiley +1 more source
Neonatal hearing screening in high-risk patients with otoacoustic emissions: evaluation of results [PDF]
, 2015 Resumen Objetivo: evaluar la efectividad del programa de tamizaje auditivo del Homic en pacientes de alto riesgo de hipoacusia neurosensorial, el cual está basado en la realización de otoemisiones acústicas Diseño: estudio de cohorte retrospectiva, en ...
Diaz Patiño, Diana Patricia +6 more
core
Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet +10 more
wiley +1 more source
Rehabilitation with Cochlear Implant in Patient with Harboyan Syndrome
International Archives of Otorhinolaryngology, 2013 Background Harboyan syndrome, defined as congenital corneal dystrophy associated with progressive sensorineural hearing loss, was first described by Harboyan in 1971.
Lauren Medeiros Paniagua +3 more
doaj +1 more source
Бюллетень сибирской медицины, 2020 The purpose of the research was to identify changes in immune and hormonal regulation in patients with hand-arm vibration syndrome and sensorineural hearing loss to substantiate informative biomarkers.Materials and methods.
G. M. Bodienkova, S. I. Kurchevenko
doaj +1 more source
Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China. [PDF]
PLoS ONE, 2016 The aim of this study was to evaluate the GoldenGate microarray as a diagnostic tool and to elucidate the contribution of the genes on this array to the development of both nonsyndromic and syndromic sensorineural hearing loss in China.We developed a ...
Hong Wu +11 more
doaj +1 more source
Hereditary sensorineural hearing loss in a bird [PDF]
Naturwissenschaften, 1994 The avian cochlea is the principal model for the investigation of hair-cell regeneration and the recovery of function in the vertebrate auditory periphery [1]. This capacity for repair in birds would seem to preclude permanent sensorineural hearing loss involving hair cells, which is the most common cause of hearing disabilities in humans [2]. Here, we
Gleich, Otto +2 more
openaire +3 more sources