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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2021
The genetic architecture of Plakophilin 2 cardiomyopathyAnnika M Dries, Anna Kirillova, Chloe M Reuter, et al.
Human Mutation|November 6, 2022
KBTBD13 is a novel cardiomyopathy geneJosine M de Winter, Karlijn Bouman, Joshua Strom, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|July 29, 2023
Design and characteristics of the prophylactic intra-operative ventricular arrhythmia ablation in high-risk LVAD candidates (PIVATAL) trialDavid T Huang, Igor Gosev, Katherine L Wood, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 25, 2014
Extensive drug resistance acquired during treatment of multidrug-resistant tuberculosisJ Peter Cegielski, Tracy Dalton, Martin Yagui, et al.
Ophthalmology. Retina|February 16, 2020
Late-Onset Retinal Findings and Complications in Untreated Retinopathy of PrematurityAbdualrahman E Hamad, Omar Moinuddin, Michael P Blair, et al.
Genome Medicine|September 18, 2023
Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to humanJulia E Niskanen, Åsa Ohlsson, Ingrid Ljungvall, et al.
European Heart Journal|October 27, 2015
Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriersGodelieve R F Claes, Florence H J van Tienen, Patrick Lindsey, et al.
Circulation. Cardiovascular Genetics|August 10, 2017
Lamin A/C-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder MutationEdgar T Hoorntje, Ilse A Bollen, Daniela Q Barge-Schaapveld, et al.
Circulation|February 24, 2025
Left Ventricular Entry to Reduce Brain Lesions During Catheter Ablation: A Randomized TrialGregory M Marcus, Roderick Tung, Edward P Gerstenfeld, et al.
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