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6721
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6722
The impact of age-related hearing loss on structural neuroanatomy: A meta-analysis
Published 2022-08-01Get full text
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6723
Real-World Hearing Aid Usage Patterns and Smartphone Connectivity
Published 2021-08-01Get full text
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6724
Occupational noise-induced hearing loss in China: a systematic review and meta-analysis
Published 2020-09-01“…The prevalence of occupational NIHL in China was 21.3%, of which 30.2% was related to high-frequency NIHL (HFNIHL), 9.0% to speech-frequency NIHL and 5.8% to noise-induced deafness. Among manufacturing workers, complex noise contributed to greater HFNIHL than Gaussian noise (overall weighted OR (OR)=1.95). …”
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6726
Hyperviscosity Syndrome Induced Bilateral Visual and Auditory Impairment in Therapy Resistant Waldenström Macroglobulinemia with MYD88 and CXCR4 Mutations
Published 2023-12-01“…We report a 69-year-old female with MYD88 and CXCR4-mutant WM who developed HVS resulting in bilateral blindness and deafness associated with neurologic manifestations including confusion, severe generalized weakness, and imbalance. …”
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6727
Self-care goals proposition and achievement by patients undergoing oral anticoagulation during an educational intervention based on empowerment
Published 2021-11-01“…The exclusion criteria were impossibility of verbal communication, deafness, blindness or health problems that could compromise attendance at the AC. …”
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6728
Relationship of Hearing Impairment in Patients with Lamivudine Therapy: A Systematic Review and Meta-analysis
Published 2022-12-01“…A comprehensive database search (PubMed, PubMed Central, Cochrane review, Google scholar and Embase) was conducted to identify the relevant literature published on HL and were searched for keywords related to lamivudine and HL- ‘lamivudine and hearing loss’, ‘lamivudine and deafness’, ‘lamivudine and hypoacusis’, ‘lamivudine and hearing impairment’ and ’lamivudine and ototoxicity’ for searching the data. …”
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6729
Telemedicine for Adults With Cochlear Implants in the United Kingdom (CHOICE): Protocol for a Prospective Interventional Multisite Study
Published 2022-04-01“… BackgroundCochlear implants provide hearing to approximately 750,000 people with deafness worldwide; these patients require lifelong follow-up. …”
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6730
The S2–S3 Loop of Kv7.4 Channels Is Essential for Calmodulin Regulation of Channel Activation
Published 2021-01-01“…Mutations in Kv7.4 channels result in inherited progressive deafness in humans. Calmodulin (CaM) is crucial for regulating Kv7 channels, but how CaM affects Kv7 activity has remained unclear. …”
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6731
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6732
Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design
Published 2021-12-01Get full text
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6733
OPRA-RS: A Hearing-Aid Fitting Method Based on Automatic Speech Recognition and Random Search
Published 2022-02-01Get full text
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6734
Método de prevenção de lesão nasal causada por CPAP em recém-nascido pré-termo: relato de caso
Published 2013-02-01Get full text
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6735
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6736
Cyclodextrins and Iatrogenic Hearing Loss: New Drugs with Significant Risk
Published 2017-11-01Get full text
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6737
Key Genes and Pathways Associated With Inner Ear Malformation in SOX10 p.R109W Mutation Pigs
Published 2018-06-01Get full text
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6738
Evidence of Authorship on Messages in Facilitated Communication: A Case Report Using Accelerometry
Published 2021-01-01“…A 17-year-old boy diagnosed with congenital deafness, ASD, and developmental delay, and his facilitator, were equipped with small accelerometers fixed on their index finger, aimed at transforming index acceleration along the three spatial axes into electric signals. …”
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6739
Development of the vapor film thickness correlation in porous corrosion deposits on the cladding in PWR
Published 2022-12-01Get full text
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6740
Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus
Published 2021-09-01“…Furthermore, two Han Chinese pedigrees with maternally inherited diabetes and deafness (MIDD) were reported by clinical and genetic assessments.Results: A total of 49 genetic variants in mt-tRNA genes were identified; among them, 31 variants (17 pathogenic/likely pathogenic) were absent in controls, located at extremely conserved nucleotides, may have potential structural and functional significance, thereby considered to be T2DM-associated variants. …”
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