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J Abrams

Showing results (791-800 of 808) with videos related to

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European Heart Journal|February 8, 2017
Proposed Standardized Neurological Endpoints for Cardiovascular Clinical Trials: An Academic Research Consortium InitiativeAlexandra J Lansky, Steven R Messé, Adam M Brickman, et al.
Journal of the American College of Cardiology|February 11, 2017
Proposed Standardized Neurological Endpoints for Cardiovascular Clinical Trials: An Academic Research Consortium InitiativeAlexandra J Lansky, Steven R Messé, Adam M Brickman, et al.
Circulation|April 17, 2026
The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry AnalysisRobert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Nature Genetics|July 14, 2015
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorderAlexander J Abrams, Robert B Hufnagel, Adriana Rebelo, et al.
Brain : a Journal of Neurology|November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.
Circulation|July 25, 2024
Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS StudyRachel Lampert, Sharlene Day, Barbara Ainsworth, et al.
European Heart Journal|July 31, 2018
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroupsAlban-Elouen Baruteau, Florence Kyndt, Elijah R Behr, et al.
Circulation|July 23, 2020
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of <i>CASQ2</i>-Catecholaminergic Polymorphic Ventricular TachycardiaKevin Ng, Erron W Titus, Krystien V Lieve, et al.
Circulation. Genomic and Precision Medicine|May 13, 2022
Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International StudyMarine Tortigue, Lynne E Nield, Matilde Karakachoff, et al.
European Heart Journal|September 17, 2024
Clinical features and outcomes in carriers of pathogenic desmoplakin variantsAlessio Gasperetti, Richard T Carrick, Alexandros Protonotarios, et al.
Pageof 81

Showing results (791-800 of 808) with videos related to

Sort By:
Pageof 81
European Heart Journal|February 8, 2017
Proposed Standardized Neurological Endpoints for Cardiovascular Clinical Trials: An Academic Research Consortium InitiativeAlexandra J Lansky, Steven R Messé, Adam M Brickman, et al.
Journal of the American College of Cardiology|February 11, 2017
Proposed Standardized Neurological Endpoints for Cardiovascular Clinical Trials: An Academic Research Consortium InitiativeAlexandra J Lansky, Steven R Messé, Adam M Brickman, et al.
Circulation|April 17, 2026
The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry AnalysisRobert Przybylski, Gabrielle Norrish, Brian Claggett, et al.
Nature Genetics|July 14, 2015
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorderAlexander J Abrams, Robert B Hufnagel, Adriana Rebelo, et al.
Brain : a Journal of Neurology|November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.
Circulation|July 25, 2024
Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS StudyRachel Lampert, Sharlene Day, Barbara Ainsworth, et al.
European Heart Journal|July 31, 2018
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroupsAlban-Elouen Baruteau, Florence Kyndt, Elijah R Behr, et al.
Circulation|July 23, 2020
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of <i>CASQ2</i>-Catecholaminergic Polymorphic Ventricular TachycardiaKevin Ng, Erron W Titus, Krystien V Lieve, et al.
Circulation. Genomic and Precision Medicine|May 13, 2022
Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International StudyMarine Tortigue, Lynne E Nield, Matilde Karakachoff, et al.
European Heart Journal|September 17, 2024
Clinical features and outcomes in carriers of pathogenic desmoplakin variantsAlessio Gasperetti, Richard T Carrick, Alexandros Protonotarios, et al.
Pageof 81