Showing 6,721 - 6,740 results of 6,901 for search '"deaf"', query time: 0.20s Refine Results
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    Occupational noise-induced hearing loss in China: a systematic review and meta-analysis by Yong Hu, Jiena Zhou, Zhihao Shi, Lifang Zhou, Meibian Zhang

    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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  5. 6725
  6. 6726

    Hyperviscosity Syndrome Induced Bilateral Visual and Auditory Impairment in Therapy Resistant Waldenström Macroglobulinemia with MYD88 and CXCR4 Mutations by Plante MM, Kimbrough EO, Agarwal AK, Jiang L, Bourgeois K, Stamper GC, Stewart MW, Tun HW

    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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  7. 6727

    Self-care goals proposition and achievement by patients undergoing oral anticoagulation during an educational intervention based on empowerment by Mayara O. ORTIZ, Josiane M. COSTA, Daniella V. NASCIMENTO, Carolina B. FERREIRA, Thais R. CORREIA, Caryne M. BERTOLLO, Maria A. MARTINS

    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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  8. 6728

    Relationship of Hearing Impairment in Patients with Lamivudine Therapy: A Systematic Review and Meta-analysis by Mahesh Namdeo Belhekar, Kalpesh K Joshi

    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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  9. 6729

    Telemedicine for Adults With Cochlear Implants in the United Kingdom (CHOICE): Protocol for a Prospective Interventional Multisite Study by Helen Cullington, Padraig Kitterick, Philippa Darnton, Tracy Finch, Kate Greenwell, Carol Riggs, Mark Weal, Dawn-Marie Walker, Andrew Sibley

    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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  10. 6730

    The S2–S3 Loop of Kv7.4 Channels Is Essential for Calmodulin Regulation of Channel Activation by Wenhui Zhuang, Zhiqiang Yan, Zhiqiang Yan

    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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    Evidence of Authorship on Messages in Facilitated Communication: A Case Report Using Accelerometry by Patrick Faure, Thierry Legou, Bruno Gepner

    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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  19. 6739
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    Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus by Lin L, Zhang D, Jin Q, Teng Y, Yao X, Zhao T, Xu X, Jin Y

    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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