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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 8, 2024. (Total: 234193Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Coronary artery disease and SCN5A[original query]
Allelic variants of SCN5A and risk of sudden cardiac arrest in patients with coronary artery disease.
Heart rhythm : the official journal of the Heart Rhythm Society 2006 Jun 3 (6): 697-700.
Stecker Eric C, Sono Megan, Wallace Erin, Gunson Karen, Jui Jonathan, Chugh Sumeet
Mutation analysis ion channel genes ventricular fibrillation survivors with coronary artery disease.
Pacing and clinical electrophysiology : PACE 2011 Jun 34 (6): 742-9.
Novotny Tomas, Kadlecova Jitka, Raudenska Martina, Bittnerova Alexandra, Andrsova Irena, Florianova Alena, Vasku Anna, Neugebauer Petr, Kozak Milan, Sepsi Milan, Krivan Lubomir, Gaillyova Renata, Spinar Jindri
Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death.
The American journal of cardiology 2019 Mar .
Tamariz Leonardo, Balda Javier, Pareja Dennise, Palacio Ana, Myerburg Robert J, Conway Douglas, Davis Lea, Goldberger Jeffrey
Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction.
Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2020 Apr .
Foddha Hajer, Bouzidi Nadia, Foddha Abdelhak, Chouchene Saoussen, Touhami Rahma, Leban Nadia, Maatoug Mohamed Faouzi, Gamra Habib, Ferchichi Salima, Chibani Jemni Ben, Khelil Amel H
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