Showing results (221-230 of 436) with videos related to

Sort By:
Pageof 44
American Heart Journal|January 29, 2000
Design and implementation of the North American Pediatric Cardiomyopathy RegistryM A Grenier, S K Osganian, G F Cox, et al.
Texas Heart Institute Journal|January 1, 1995
Postpericardiotomy syndrome in pediatric heart transplant recipients. Immunologic characteristicsA K Cabalka, H M Rosenblatt, J A Towbin, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|February 1, 1996
Diagnosis, surveillance, and epidemiologic evaluation of viral infections in pediatric cardiac transplant recipients with the use of the polymerase chain reactionK O Schowengerdt, J Ni, S W Denfield, et al.
Circulation|December 1, 1994
Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 familiesJ A Towbin, H Li, R T Taggart, et al.
Journal of Cardiovascular Electrophysiology|March 19, 2004
Phenotypic characterization of a large European family with Brugada syndrome displaying a sudden unexpected death syndrome mutation in SCN5A:Kui Hong, Antonio Berruezo-Sanchez, Naravat Poungvarin, et al.
Genomics|August 1, 1992
Identification of new markers in Xp21 between DXS28 (C7) and DMDK C Worley, J A Towbin, X M Zhu, et al.
Molecular Genetics and Metabolism|December 15, 2005
Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethoninJ Martijn Bos, Rainer N Poley, Melissa Ny, et al.
Circulation|October 26, 2005
Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophyJohn L Jefferies, Benjamin W Eidem, John W Belmont, et al.
International Journal of Cardiology|November 9, 2021
Combining whole exome sequencing with in silico analysis and clinical data to identify candidate variants in pediatric left ventricular noncompactionJohn Collyer, Fuyi Xu, Undral Munkhsaikhan, et al.
Pageof 44