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Journal of the American College of Cardiology|August 4, 2022
Deep Learning Electrocardiographic Analysis for Detection of Left-Sided Valvular Heart DiseasePierre Elias, Timothy J Poterucha, Vijay Rajaram, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 13, 2026
Soluble SORL1 in cerebrospinal fluid as a marker for functional impact of rare SORL1 variantsMatthijs W J de Waal, Sven J van der Lee, Melanie Lunding, et al.
The Journal of Rheumatology|November 19, 2013
Responsiveness in rheumatoid arthritis. a report from the OMERACT 11 ultrasound workshopAnnamaria Iagnocco, Esperanza Naredo, Richard Wakefield, et al.
Diabetes Care|April 11, 2025
Subphenotype-Dependent Benefits of Bariatric Surgery for Individuals at Risk for Type 2 DiabetesLeontine Sandforth, Violeta Raverdy, Arvid Sandforth, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|September 11, 2024
Influence of implant strategy on the transition from temporary left ventricular assist device to durable mechanical circulatory supportA L Meyer, D Lewin, M Billion, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 3, 2019
The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort EffectSanne W Ten Broeke, Mar Rodríguez-Girondo, Manon Suerink, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|May 18, 2024
Exploring a Preliminary Set of Indicators to Measure Adolescent Health: Results From a 12-Country Feasibility StudyAnna E Kågesten, Andrew D Marsh, Simone Storey, et al.
American Journal of Human Genetics|June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.
Trends in Neurosciences|April 26, 2018
Progress in Understanding and Treating SCN2A-Mediated DisordersStephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, et al.
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