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Gut|February 14, 2018
Gastrointestinal ultrasound in inflammatory bowel disease: an underused resource with potential paradigm-changing applicationRobert Venning Bryant, Antony B Friedman, Emily Kate Wright, et al.The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|July 31, 2003
Retention, adherence, and compliance: special needs of HIV-infected adolescent girls and young womenSally Dodds, T Blakley, J M Lizzotte, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.Genes|July 27, 2024
Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1-Deficient MiceRabia Faridi, Rizwan Yousaf, Sayaka Inagaki, et al.Journal of Cognitive Neuroscience|May 9, 2023
Listening to Yourself and Watching Your Tongue: Distinct Abilities and Brain Regions for Monitoring Semantic and Phonological Speech ErrorsJoshua D McCall, Andrew T DeMarco, Ayan S Mandal, et al.BMJ Open|September 12, 2025
Ages of sitting and walking milestone attainment in typically developing children worldwide: protocol for a scoping reviewJordan Wickstrom, Izza Choudhry, Emma J Leone, et al.American Journal of Health Promotion : AJHP|April 1, 2025
Walking Interventions and Cognitive Health in Older Adults: A Systematic Review of Randomized Controlled TrialsJongwon Lee, Delia West, Christine Pellegrini, et al.The Journal of Biological Chemistry|March 30, 2001
Yeast Mps1p phosphorylates the spindle pole component Spc110p in the N-terminal domainD B Friedman, J W Kern, B J Huneycutt, et al.Frontiers in Public Health|January 22, 2025
Reflecting on partnerships established and sustained over four cycles of a federally funded cancer prevention and control research program: lessons learned for community-academic networksSwann Arp Adams, Lauren Workman, Mayank Sakhuja, et al.Journal of Medical Genetics|February 7, 2006
Mutations of human TMHS cause recessively inherited non-syndromic hearing lossM I Shabbir, Z M Ahmed, S Y Khan, et al.Pageof 97