Showing results (361-370 of 723) with videos related to

Sort By:
Pageof 73
Journal of Cardiovascular Electrophysiology|May 23, 2013
Mutation location effect on severity of phenotype during exercise testing in type 1 long-QT syndrome: impact of transmembrane and C-loop locationZachary W M Laksman, Robert M Hamilton, Priya Chockalingam, et al.
American Journal of Medical Genetics. Part A|November 18, 2008
Predictive genetic testing for cardiovascular diseases: impact on carrier childrenTineke M Meulenkamp, Aad Tibben, Eline D Mollema, et al.
Heart Rhythm|March 26, 2008
Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutationZahurul A Bhuiyan, Tarek S Momenah, Qiuming Gong, et al.
Heart Rhythm|October 15, 2014
Syncope in Brugada syndrome: prevalence, clinical significance, and clues from history taking to distinguish arrhythmic from nonarrhythmic causesLouise R A Olde Nordkamp, Arja S Vink, Arthur A M Wilde, et al.
European Journal of Medical Genetics|November 8, 2021
Andersen-Tawil syndrome: Overlapping clinical features with Noonan syndrome?A S van der Werf-'t Lam, A van Haeringen, T Rinnen, et al.
Heart Rhythm|April 4, 2020
SARS-CoV-2, COVID-19, and inherited arrhythmia syndromesCheng-I Wu, Pieter G Postema, Elena Arbelo, et al.
Heart Rhythm|May 15, 2018
Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variantsBelinda Gray, Can Hasdemir, Jodie Ingles, et al.
Computers in Biology and Medicine|February 19, 2021
Improving electrocardiogram-based detection of rare genetic heart disease using transfer learning: An application to phospholamban p.Arg14del mutation carriersRicardo R Lopes, Hidde Bleijendaal, Lucas A Ramos, et al.
Community Genetics|June 1, 2005
High distress in parents whose children undergo predictive testing for long QT syndromeKarin S W H Hendriks, F J M Grosfeld, A A M Wilde, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Somatic mosaicism contributes to phenotypic variation in Timothy syndromeSusan P Etheridge, Neil E Bowles, Cammon B Arrington, et al.
Pageof 73