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ChannelopathiesDesign of Bioactive Peptides from Naturally Occurring -Conotoxin StructuresHRS policy statement: clinical cardiac electrophysiology fellowship curriculum: update 2011Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology.Determining the pathogenicity of genetic variants associated with cardiac channelopathies.Estrogen-related receptor α (ERRα) and ERRγ are essential coordinators of cardiac metabolism and function.Ionotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases.New Genetic Insights into Congenital Heart Disease.Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic InvestigationParalogous annotation of disease-causing variants in long QT syndrome genes.New clinical molecular diagnostic methods for congenital and inherited heart disease.Negative autopsy and sudden cardiac death.Mutational consequences of aberrant ion channels in neurological disorders.Modeling the human Nav1.5 sodium channel: structural and mechanistic insights of ion permeation and drug blockade.Precision medicine approach to genetic cardiomyopathy.Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome.Ion channels, long QT syndrome and arrhythmogenesis in ageing.Unmasking the molecular link between arrhythmogenic cardiomyopathy and Brugada syndrome.Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac DeathA hypertrophic and dilated cardiomyopathic sudden cardiac death case; de novo mutations in TTN and SGCD genes.Risk of cardiovascular disease in family members of young sudden cardiac death victims.Molecular Autopsy for Sudden Death in the Young: Is Data Aggregation the Key?Ion channel phosphorylopathy: a link between genomic variation and human disease.Sudden cardiac death with stress and restraint: The association with sudden adult death syndrome, cardiomyopathy and coronary artery disease.QT interval and the risk of myocardial infarction and all-cause death: a cohort study.Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on May 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Genetics and cardiac channelopathies.
@en
Genetics and cardiac channelopathies.
@nl
type
label
Genetics and cardiac channelopathies.
@en
Genetics and cardiac channelopathies.
@nl
prefLabel
Genetics and cardiac channelopathies.
@en
Genetics and cardiac channelopathies.
@nl
P2860
P50
P1433
P1476
Genetics and cardiac channelopathies
@en
P2093
Anna Iglesias
Ramon Brugada
P2860
P2888
P304
P356
10.1097/GIM.0B013E3181D81636
P407
P577
2010-05-01T00:00:00Z
P6179
1039128654