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Arthur A Wilde

Showing results (61-70 of 73) with videos related to

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Circulation. Cardiovascular Genetics|August 10, 2017
<i>Lamin A/C</i>-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. Arrhythmia and Electrophysiology|August 11, 2017
Loss-of-Function <i>KCNE2</i> Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?Jason D Roberts, Andrew D Krahn, Michael J Ackerman, et al.
Circulation. Cardiovascular Genetics|March 31, 2015
Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family MembersJudith A Groeneweg, Aditya Bhonsale, Cynthia A James, et al.
European Heart Journal|May 31, 2019
Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrestChristian van der Werf, Krystien V Lieve, J Martijn Bos, 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.
European Heart Journal|August 29, 2014
Atlas of the clinical genetics of human dilated cardiomyopathyJan Haas, Karen S Frese, Barbara Peil, et al.
Cardiovascular Research|December 5, 2021
European Society of Cardiology guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 1-epidemiology, pathophysiology, and diagnosis, Colin Baigent, Stephan Windecker, et al.
Nature Genetics|July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
European Heart Journal|December 19, 2025
Catecholaminergic polymorphic ventricular tachycardia mediated by ryanodine receptor 2: a validated risk stratificationKrystien V Lieve, Christian van der Werf, Dania Kallas, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Circulation. Cardiovascular Genetics|August 10, 2017
<i>Lamin A/C</i>-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. Arrhythmia and Electrophysiology|August 11, 2017
Loss-of-Function <i>KCNE2</i> Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?Jason D Roberts, Andrew D Krahn, Michael J Ackerman, et al.
Circulation. Cardiovascular Genetics|March 31, 2015
Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family MembersJudith A Groeneweg, Aditya Bhonsale, Cynthia A James, et al.
European Heart Journal|May 31, 2019
Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrestChristian van der Werf, Krystien V Lieve, J Martijn Bos, 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.
European Heart Journal|August 29, 2014
Atlas of the clinical genetics of human dilated cardiomyopathyJan Haas, Karen S Frese, Barbara Peil, et al.
Cardiovascular Research|December 5, 2021
European Society of Cardiology guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 1-epidemiology, pathophysiology, and diagnosis, Colin Baigent, Stephan Windecker, et al.
Nature Genetics|July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathyRafik Tadros, Sean L Zheng, Christopher Grace, et al.
European Heart Journal|December 19, 2025
Catecholaminergic polymorphic ventricular tachycardia mediated by ryanodine receptor 2: a validated risk stratificationKrystien V Lieve, Christian van der Werf, Dania Kallas, et al.
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