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Clinical Pharmacology and Therapeutics|January 16, 2022
Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2C19 Genotype and Clopidogrel Therapy: 2022 UpdateCraig R Lee, Jasmine A Luzum, Katrin Sangkuhl, et al.
Thrombosis and Haemostasis|December 16, 2014
A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical recordJason H Karnes, Robert M Cronin, Jerome Rollin, et al.
The Journal of Clinical Investigation|May 10, 2008
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansHiroshi Watanabe, Tamara T Koopmann, Solena Le Scouarnec, et al.
JAMA Cardiology|September 8, 2021
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia GenesZachary T Yoneda, Katherine C Anderson, Joseph A Quintana, et al.
Blood Advances|May 9, 2022
Genome-wide association study of platelet factor 4/heparin antibodies in heparin-induced thrombocytopeniaJason B Giles, Heidi E Steiner, Jerome Rollin, et al.
Circulation. Arrhythmia and Electrophysiology|January 17, 2012
A connexin40 mutation associated with a malignant variant of progressive familial heart block type INaomasa Makita, Akiko Seki, Naokata Sumitomo, et al.
Circulation. Arrhythmia and Electrophysiology|February 21, 2020
Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation AblationM Benjamin Shoemaker, Daniela Husser, Carolina Roselli, et al.
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