Association of Hearing Impairment and 24-Hour Total Movement Activity in a Representative Sample of US Adults
Sign Up to like & getrecommendations! Published in 2022 at "JAMA Network Open"
DOI: 10.1001/jamanetworkopen.2022.2983
Abstract: Key Points Question Is hearing loss associated with lower levels of physical activity? Findings In this cross-sectional analysis of 2490 US adults aged 30 to 69 years, worse hearing, as defined by pure-tone audiometry, was… read more here.
Keywords: impairment hour; hour total; hearing impairment; physical activity ... See more keywords
Hearing impairment and tinnitus among older construction workers employed at DOE facilities.
Sign Up to like & getrecommendations! Published in 2022 at "American journal of industrial medicine"
DOI: 10.1002/ajim.23406
Abstract: BACKGROUND Few studies have defined the risk of hearing impairment and tinnitus after retirement. This report measures hearing impairment and tinnitus prevalence among older construction trades workers. METHODS The study cohort included 21,340 participants in… read more here.
Keywords: impairment tinnitus; prevalence; hearing impairment; tinnitus ... See more keywords
The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype
Sign Up to like & getrecommendations! Published in 2017 at "Brain and Behavior"
DOI: 10.1002/brb3.859
Abstract: Mutations in mitochondrial DNA cause a variety of clinical phenotypes ranging from a mild hearing impairment (HI) to severe encephalomyopathy. The MT‐TS1 gene is a hotspot for mutations causing HI. The m.7510T>C mutation in MT‐TS1… read more here.
Keywords: hearing impairment; mutation hearing; impairment complex; 7510t mutation ... See more keywords
Baseline audiometric assessment of newly diagnosed nasopharyngeal carcinoma patients: a multicentre cross‐sectional study
Sign Up to like & getrecommendations! Published in 2025 at "International Journal of Cancer"
DOI: 10.1002/ijc.35358
Abstract: Hearing impairment is one of the most common chief complaints in newly diagnosed nasopharyngeal carcinoma (NPC) patients, but baseline audiometric assessments are seldom reported. This study aims to investigate the prevalence of hearing impairment in… read more here.
Keywords: hearing; newly diagnosed; hearing impairment; baseline audiometric ... See more keywords
Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNAAla 5601C>T and tRNALeu(CUN) 12311T>C mutations
Sign Up to like & getrecommendations! Published in 2022 at "Journal of Clinical Laboratory Analysis"
DOI: 10.1002/jcla.24298
Abstract: Sequence alternations in mitochondrial genomes, especially in genes encoding mitochondrial tRNA (mt‐tRNA), were the important contributors to nonsyndromic hearing loss (NSHL); however, the molecular mechanisms remained largely undetermined. read more here.
Keywords: nonsyndromic hearing; impairment may; maternally transmitted; hearing impairment ... See more keywords
Custom Next‐Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys
Sign Up to like & getrecommendations! Published in 2022 at "Molecular Genetics & Genomic Medicine"
DOI: 10.1002/mgg3.1868
Abstract: In the Tunisian population, the molecular analysis of hearing impairment remains based on conventional approaches, which makes the task laborious and enormously expensive. Exploration of the etiology of Hearing Impairment and the early diagnosis of… read more here.
Keywords: hearing impairment; custom next; next generation; generation sequencing ... See more keywords
[Speech audiometry in expert assessment of hearing impairment].
Sign Up to like & getrecommendations! Published in 2017 at "HNO"
DOI: 10.1007/s00106-016-0239-2
Abstract: In the assessment process of hearing impairment the medical expert has to verify its causality and to quantify its severity as hearing loss in percentage. Based on the determined hearing loss in percentage, the degree… read more here.
Keywords: expert assessment; hearing loss; hearing impairment; loss ... See more keywords
Hearing impairment amongst people with Osteogenesis Imperfecta in Germany
Sign Up to like & getrecommendations! Published in 2024 at "European Archives of Oto-Rhino-Laryngology"
DOI: 10.1007/s00405-024-08983-5
Abstract: Hearing impairment concerns a relevant percentage of individuals with Osteogenesis Imperfecta (OI). When looking at the current literature, the percentage of affected individuals with OI varies greatly from 32 to 58% of patients having mild… read more here.
Keywords: impairment amongst; hearing impairment; hearing loss; amongst people ... See more keywords
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
Sign Up to like & getrecommendations! Published in 2018 at "Human Genetics"
DOI: 10.1007/s00439-018-1965-1
Abstract: ATP2B2 encodes the PMCA2 Ca2+ pump that plays an important role in maintaining ion homeostasis in hair cells among others by extrusion of Ca2+ from the stereocilia to the endolymph. Several mouse models have been… read more here.
Keywords: hearing impairment; variants atp2b2; loss function; rapidly progressive ... See more keywords
Neurocognitive assessment in relation to hearing impairment and retinal neurodegeneration
Sign Up to like & getrecommendations! Published in 2025 at "Neurological Sciences"
DOI: 10.1007/s10072-025-08305-5
Abstract: Sensory impairments are significant contributors to cognitive dysfunction, but the relationship between cognitive decline and various forms of neurosensory degeneration remains poorly understood. This study aimed to evaluate retinal layer neurodegeneration and hearing impairment in… read more here.
Keywords: retinal neurodegeneration; khz khz; hearing impairment; neurodegeneration ... See more keywords
Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations
Sign Up to like & getrecommendations! Published in 2017 at "Journal of Community Genetics"
DOI: 10.1007/s12687-017-0299-3
Abstract: Hereditary hearing impairment (HI) caused by recessive GJB2 mutations is a frequent sensory disorder. The results of the molecular-based studies of HI are widely used in various genetic test systems. However, the ethical aspects are… read more here.
Keywords: opinions hearing; gjb2 mutations; hearing impairment; hearing parents ... See more keywords