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Circulation. Arrhythmia and Electrophysiology|July 14, 2018
Localized Structural Alterations Underlying a Subset of Unexplained Sudden Cardiac DeathMichel Haïssaguerre, Mélèze Hocini, Ghassen Cheniti, et al.
Brain : a Journal of Neurology|December 4, 2019
Deficiencies in vesicular transport mediated by TRAPPC4 are associated with severe syndromic intellectual disabilityNicole J Van Bergen, Yiran Guo, Noraldin Al-Deri, et al.
American Journal of Human Genetics|July 9, 2013
Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disabilityNina Bögershausen, Nassim Shahrzad, Jessica X Chong, et al.
The New England Journal of Medicine|May 9, 2008
Sudden cardiac arrest associated with early repolarizationMichel Haïssaguerre, Nicolas Derval, Frederic Sacher, et al.
Circulation. Arrhythmia and Electrophysiology|January 30, 2026
Impact of Congenital Substrate 3D Imaging Reconstruction to Guide VT Catheter Ablation: The CORECA StudyFrancis Bessière, Nicolas Combes, Hubert Cochet, et al.
JACC. Clinical Electrophysiology|December 21, 2019
Ultra-High-Density Activation Mapping to Aid Isthmus Identification of Atrial Tachycardias in Congenital Heart DiseaseClaire A Martin, Arthur Yue, Ruairidh Martin, et al.
European Heart Journal|March 6, 2024
Implantable loop recorders in patients with Brugada syndrome: the BruLoop studyMarco Bergonti, Frederic Sacher, Elena Arbelo, et al.
Nature Chemical Biology|February 26, 2020
A drug discovery platform to identify compounds that inhibit EGFR triple mutantsPunit Saraon, Jamie Snider, Yannis Kalaidzidis, et al.
The New England Journal of Medicine|September 21, 2020
KRASG12C Inhibition with Sotorasib in Advanced Solid TumorsDavid S Hong, Marwan G Fakih, John H Strickler, et al.
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