Showing results (401-410 of 722) with videos related to

Sort By:
Pageof 73
G3 (Bethesda, Md.)|May 23, 2013
Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association studyKeyue Ding, Mariza de Andrade, Teri A Manolio, et al.
Journal of the American Medical Informatics Association : JAMIA|June 16, 2011
Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarinHua Xu, Min Jiang, Matt Oetjens, et al.
Plos One|June 10, 2010
Rates and reasons for early change of first HAART in HIV-1-infected patients in 7 sites throughout the Caribbean and Latin AmericaCarina Cesar, Bryan E Shepherd, Alejandro J Krolewiecki, et al.
Anesthesiology|January 8, 2013
Does low-dose droperidol increase the risk of polymorphic ventricular tachycardia or death in the surgical patient?Gregory A Nuttall, Ann M Malone, Carrie A Michels, et al.
International Journal of Cardiology|July 9, 2016
Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C-encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window currentAndrew P Landstrom, Nicole J Boczek, Dan Ye, et al.
Heart Rhythm|March 16, 2010
Sudden infant death syndrome-associated mutations in the sodium channel beta subunitsBi-Hua Tan, Kavitha N Pundi, David W Van Norstrand, et al.
Circulation. Cardiovascular Genetics|December 15, 2017
Technical Advances for the Clinical Genomic Evaluation of Sudden Cardiac Death: Verification of Next-Generation Sequencing Panels for Hereditary Cardiovascular Conditions Using Formalin-Fixed Paraffin-Embedded Tissues and Dried Blood SpotsLinnea M Baudhuin, Charles Leduc, Laura J Train, et al.
Heart Rhythm|September 1, 2009
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic testJamie D Kapplinger, David J Tester, Benjamin A Salisbury, et al.
Heart Rhythm|November 26, 2013
A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylationDaniel C Bartos, John R Giudicessi, David J Tester, et al.
Circulation. Arrhythmia and Electrophysiology|March 4, 2014
Pathogeneses of sudden cardiac death in national collegiate athletic association athletesKimberly G Harmon, Jonathan A Drezner, Joseph J Maleszewski, et al.
Pageof 73