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Clinical and Translational Medicine
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June 29, 2021
A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype
Zeina R Al Sayed, Mariam Jouni, Jean-Baptiste Gourraud, et al.
Journal of the American College of Cardiology
|
August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy
Annalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Journal of the American Heart Association
|
June 12, 2016
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome
Vincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, et al.
Human Molecular Genetics
|
January 29, 2010
Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease
Natalie J Prescott, Katherine M Dominy, Michiaki Kubo, et al.
JACC. Clinical Electrophysiology
|
July 22, 2023
Left Ventricular Abnormal Substrate in Brugada Syndrome
Ghassen Cheniti, Michel Haissaguerre, Christian Dina, et al.
Cardiovascular Research
|
August 4, 2025
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants
Taisuke Ishikawa, Hiroki Kimoto, Akiko Seki, et al.
Clinical Genetics
|
November 10, 2020
A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet-Biedl syndrome
Clarisse Delvallée, Samuel Nicaise, Manuela Antin, et al.
Human Molecular Genetics
|
February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome
Solena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
American Journal of Human Genetics
|
August 16, 2016
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy
Anne Guimier, Christopher T Gordon, François Godard, et al.
Genome Research
|
November 24, 2006
Accurate and reliable high-throughput detection of copy number variation in the human genome
Heike Fiegler, Richard Redon, Dan Andrews, et al.
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of 14
Search research articles
Search
Showing results (71-80 of 131) with videos related to
Sort By:
Page
of 14
Clinical and Translational Medicine
|
June 29, 2021
A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype
Zeina R Al Sayed, Mariam Jouni, Jean-Baptiste Gourraud, et al.
Journal of the American College of Cardiology
|
August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy
Annalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Journal of the American Heart Association
|
June 12, 2016
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome
Vincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, et al.
Human Molecular Genetics
|
January 29, 2010
Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease
Natalie J Prescott, Katherine M Dominy, Michiaki Kubo, et al.
JACC. Clinical Electrophysiology
|
July 22, 2023
Left Ventricular Abnormal Substrate in Brugada Syndrome
Ghassen Cheniti, Michel Haissaguerre, Christian Dina, et al.
Cardiovascular Research
|
August 4, 2025
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants
Taisuke Ishikawa, Hiroki Kimoto, Akiko Seki, et al.
Clinical Genetics
|
November 10, 2020
A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet-Biedl syndrome
Clarisse Delvallée, Samuel Nicaise, Manuela Antin, et al.
Human Molecular Genetics
|
February 5, 2015
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome
Solena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, et al.
American Journal of Human Genetics
|
August 16, 2016
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy
Anne Guimier, Christopher T Gordon, François Godard, et al.
Genome Research
|
November 24, 2006
Accurate and reliable high-throughput detection of copy number variation in the human genome
Heike Fiegler, Richard Redon, Dan Andrews, et al.
Page
of 14