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Journal of Medical Virology|September 17, 2020
Lowering the transmission and spread of human coronavirusCraig Meyers, Richard Robison, Janice Milici, et al.Hepatology (Baltimore, Md.)|January 8, 2020
Applying Machine Learning in Liver Disease and Transplantation: A Comprehensive ReviewAshley Spann, Angeline Yasodhara, Justin Kang, et al.Global Change Biology|December 1, 2018
A triple trophic boost: How carbon emissions indirectly change a marine food chainZoë A Doubleday, Ivan Nagelkerken, Madeleine D Coutts, et al.Journal of Thrombosis and Haemostasis : JTH|September 4, 2014
Multicenter dose-finding and efficacy and safety outcomes in neonates and children treated with dalteparin for acute venous thromboembolismS H O'Brien, R Kulkarni, A Wallace, et al.Nutrients|November 7, 2020
Multinutrients for the Treatment of Psychiatric Symptoms in Clinical Samples: A Systematic Review and Meta-Analysis of Randomized Controlled TrialsJeanette M Johnstone, Andrew Hughes, Joshua Z Goldenberg, et al.Heart Rhythm|January 3, 2016
Brain natriuretic peptide and the risk of ventricular tachyarrhythmias in mildly symptomatic heart failure patients enrolled in MADIT-CRTAharon Medina, Arthur J Moss, Scott McNitt, et al.The American Journal of Medicine|September 8, 2015
Prevalence and Significance of Unrecognized Renal Dysfunction in Patients with Acute Coronary SyndromeZach Rozenbaum, Avi Leader, Yoram Neuman, et al.The Journal of Clinical and Aesthetic Dermatology|July 24, 2014
Retapamulin 1% Ointment and Clobetasol Propionate 0.05% Foam is More Efficacious than Vehicle Ointment and Clobetasol 0.05% Propionate Foam in the Treatment of Hand/Foot Dermatitis: A Single Center, Randomized, Double-blind StudyMadelaine Haddican, Rita V Linkner, Giselle Singer, et al.The Israel Medical Association Journal : IMAJ|December 16, 2015
High Sensitivity Cardiac Troponin T Levels after Elective Cardioversion for Atrial Fibrillation/FlutterZaza Iakobishvili, Adaya Weissler, Kiril Buturlin, et al.Genetics Research|June 7, 2016
Exome sequencing identified a novel de novo OPA1 mutation in a consanguineous family presenting with optic atrophyLior Cohen, Shay Tzur, Nitza Goldenberg-Cohen, et al.Pageof 608