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Richard D Bagnall

Showing results (1-10 of 74) with videos related to

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Epileptic Disorders : International Epilepsy Journal with Videotape|June 21, 2023
ILAE Genetic Literacy Series: Postmortem Genetic Testing in Sudden Unexpected Death in EpilepsyRichard D Bagnall, Piero Perucca,
Heart Failure Clinics|March 12, 2018
Genetic Testing for Cardiomyopathies in Clinical PracticeJodie Ingles, Richard D Bagnall, Christopher Semsarian
Clinical and Experimental Pharmacology & Physiology|September 3, 2008
Impact of multiple gene mutations in determining the severity of cardiomyopathy and heart failureTatiana Tsoutsman, Richard D Bagnall, Christopher Semsarian
International Journal of Cardiology|August 12, 2009
The role of large gene deletions and duplications in MYBPC3 and TNNT2 in patients with hypertrophic cardiomyopathyRichard D Bagnall, Laura Yeates, Christopher Semsarian
Frontiers in Neurology|August 5, 2017
Genetic Basis of Sudden Unexpected Death in EpilepsyRichard D Bagnall, Douglas E Crompton, Christopher Semsarian
Heart, Lung & Circulation|February 8, 2020
Sudden Cardiac Death in the YoungRichard D Bagnall, Emma S Singer, Jacob Tfelt-Hansen
Human Pathology|April 30, 2013
Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year reviewAngharad Evans, Richard D Bagnall, Johan Duflou, et al.
Brain Pathology (Zurich, Switzerland)|September 30, 2010
Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) casesEmily Tu, Richard D Bagnall, Johan Duflou, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2019
Correction: Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessmentJipin Das K, Jodie Ingles, Richard D Bagnall, et al.
Circulation. Genomic and Precision Medicine|January 16, 2019
Key Value of RNA Analysis of MYBPC3 Splice-Site Variants in Hypertrophic CardiomyopathyEmma S Singer, Jodie Ingles, Christopher Semsarian, et al.
Pageof 8

Showing results (1-10 of 74) with videos related to

Sort By:
Pageof 8
Epileptic Disorders : International Epilepsy Journal with Videotape|June 21, 2023
ILAE Genetic Literacy Series: Postmortem Genetic Testing in Sudden Unexpected Death in EpilepsyRichard D Bagnall, Piero Perucca,
Heart Failure Clinics|March 12, 2018
Genetic Testing for Cardiomyopathies in Clinical PracticeJodie Ingles, Richard D Bagnall, Christopher Semsarian
Clinical and Experimental Pharmacology & Physiology|September 3, 2008
Impact of multiple gene mutations in determining the severity of cardiomyopathy and heart failureTatiana Tsoutsman, Richard D Bagnall, Christopher Semsarian
International Journal of Cardiology|August 12, 2009
The role of large gene deletions and duplications in MYBPC3 and TNNT2 in patients with hypertrophic cardiomyopathyRichard D Bagnall, Laura Yeates, Christopher Semsarian
Frontiers in Neurology|August 5, 2017
Genetic Basis of Sudden Unexpected Death in EpilepsyRichard D Bagnall, Douglas E Crompton, Christopher Semsarian
Heart, Lung & Circulation|February 8, 2020
Sudden Cardiac Death in the YoungRichard D Bagnall, Emma S Singer, Jacob Tfelt-Hansen
Human Pathology|April 30, 2013
Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year reviewAngharad Evans, Richard D Bagnall, Johan Duflou, et al.
Brain Pathology (Zurich, Switzerland)|September 30, 2010
Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) casesEmily Tu, Richard D Bagnall, Johan Duflou, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2019
Correction: Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessmentJipin Das K, Jodie Ingles, Richard D Bagnall, et al.
Circulation. Genomic and Precision Medicine|January 16, 2019
Key Value of RNA Analysis of MYBPC3 Splice-Site Variants in Hypertrophic CardiomyopathyEmma S Singer, Jodie Ingles, Christopher Semsarian, et al.
Pageof 8