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Cell|July 3, 2018
Defects in the Alternative Splicing-Dependent Regulation of REST Cause DeafnessYoko Nakano, Michael C Kelly, Atteeq U Rehman, et al.Journal of the Association for Research in Otolaryngology : JARO|September 1, 2011
TRPA1-mediated accumulation of aminoglycosides in mouse cochlear outer hair cellsRuben S Stepanyan, Artur A Indzhykulian, A Catalina Vélez-Ortega, et al.Clinical Genetics|November 22, 2007
Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing lossV Labay, G Garrido, A C Madeo, et al.Journal of Acquired Immune Deficiency Syndromes (1999)|June 20, 2025
Clinical documentation of social determinants of health and its relationship with COVID-19 outcomes among people with and without HIVXueying Yang, Jiajia Zhang, Yunqing Ma, et al.Archives of Gerontology and Geriatrics|March 11, 2017
Concern about developing Alzheimer's disease or dementia and intention to be screened: An analysis of national survey dataWeizhou Tang, Kristie Kannaley, Daniela B Friedman, et al.JAMA Network Open|January 19, 2023
Prevalence of Behavioral Flags in the Electronic Health Record Among Black and White Patients Visiting the Emergency DepartmentAnish K Agarwal, Emily Seeburger, Gerald O'Neill, et al.Health Affairs (Project Hope)|April 3, 2023
Widespread Third-Party Tracking On Hospital Websites Poses Privacy Risks For Patients And Legal Liability For HospitalsAri B Friedman, Raina M Merchant, Amey Maley, et al.Skin Pharmacology : the Official Journal of the Skin Pharmacology Society|January 1, 1991
Clinical and biochemical effects of an oral leukotriene biosynthesis inhibitor (MK886) in psoriasisE M de Jong, I M van Vlijmen, J C Scholte, et al.Journal of the American Geriatrics Society|October 10, 2021
Evaluation and disposition of older adults presenting to the emergency department with abdominal painAri B Friedman, Angela T Chen, Rachel Wu, et al.American Journal of Human Genetics|July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delTA J Griffith, A A Chowdhry, K Kurima, et al.Pageof 97