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Resuscitation|June 28, 2014
Diurnal variations in incidence and outcome of out-of-hospital cardiac arrest including prior comorbidity and pharmacotherapy: a nationwide study in DenmarkLena I M Karlsson, Mads Wissenberg, Emil L Fosbøl, et al.Science Translational Medicine|May 3, 2014
Biobanks and electronic medical records: enabling cost-effective researchErica Bowton, Julie R Field, Sunny Wang, et al.Immunity, Inflammation and Disease|January 7, 2016
CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroidsAmber Dahlin, Joshua Denny, Dan M Roden, et al.Journal of the American College of Cardiology|February 25, 2014
Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndromePeter Weeke, Jonathan D Mosley, David Hanna, et al.The Journal of Allergy and Clinical Immunology|June 16, 2015
CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studiesMichael J McGeachie, Ann C Wu, Sze Man Tse, et al.Cardiovascular Research|February 19, 2015
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative studyElijah R Behr, Eleonora Savio-Galimberti, Julien Barc, 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.Nature Genetics|July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.Pageof 6