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Clinics in Sports Medicine|June 24, 2015
Something Old, Something New: Using Family History and Genetic Testing to Diagnose and Manage Athletes with Inherited Cardiovascular DiseaseMatthew J Thomas, Robert W BattleJournal of Psychosomatic Research|June 15, 2004
The contribution of expectations to motion sickness symptoms and gastric activityManda J Williamson, Matthew J Thomas, Robert M SternPlos One|March 31, 2016
α1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium CurrentJong-Il Choi, Chaojian Wang, Matthew J Thomas, et al.Biochimica Et Biophysica Acta. Proteins and Proteomics|October 7, 2021
Kinetic characterization and thermostability of C. elegans cytoplasmic and mitochondrial malate dehydrogenasesMatthew J Thomas, Emma R Cassidy, Devin S Robinson, et al.Journal of Immunology (Baltimore, Md. : 1950)|December 26, 2001
CD8 T cells inhibit IgE via dendritic cell IL-12 induction that promotes Th1 T cell counter-regulationMatthew J Thomas, Alistair Noble, Ela Sawicka, et al.European Journal of Anaesthesiology|September 11, 2010
Mortality and postoperative care after emergency laparotomyAdrian Clarke, Henry Murdoch, Matthew J Thomas, et al.Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|October 19, 2021
First Report: Rare RNF213 Variant Associated with Familial Moyamoya Disease in an African American FamilyN Abimbola Sunmonu, Naveen Kumar Ambati, Matthew J Thomas, et al.Health Care Management Science|July 10, 2020
COVID-19 scenario modelling for the mitigation of capacity-dependent deaths in intensive careRichard M Wood, Christopher J McWilliams, Matthew J Thomas, et al.Journal of the American Association for Laboratory Animal Science : JAALAS|August 4, 2006
Use of human nasal cannulas during bronchoscopy procedures as a simple method for maintaining adequate oxygen saturation in pigtailed macaques (Macaca nemestrina)Matthew J Thomas, Leon R Flanary, Bruce A Brown, et al.Retinal Cases & Brief Reports|November 13, 2014
Simultaneous fzd4 and lrp5 mutation in autosomal dominant familial exudative vitreoretinopathyEvan Stiegel, Emil A T Say, B Christian Carter, et al.Pageof 8