Risk of cardiovascular disease in family members of young sudden cardiac death victims

The Molecular Autopsy: Should the Evaluation Continue After the Funeral?

(2012) David J. Tester et al.   PEDIATRIC CARDIOLOGY

Cardiogenetic screening of first-degree relatives after sudden cardiac death in the young: a population-based approach

(2011) A. Hendrix et al.   EUROPACE

Genetics of sudden death: focus on inherited channelopathies

(2011) M. Cerrone et al.   EUROPEAN HEART JOURNAL

Sudden death: managing the patient who survives

(2011) M. Pachon et al.   HEART

Genomics of Cardiovascular Disease

(2011) Christopher J. O'Donnell et al.   NEW ENGLAND JOURNAL OF MEDICINE

The Danish National Patient Register

(2011) Elsebeth Lynge et al.   SCANDINAVIAN JOURNAL OF PUBLIC HEALTH

The Danish Civil Registration System

(2011) Carsten Bøcker Pedersen   SCANDINAVIAN JOURNAL OF PUBLIC HEALTH

Screening for, and management of, possible arrhythmogenic syndromes (channelopathies/ion channel diseases)

(2010) J. H. Svendsen et al.   EUROPACE

Nationwide study of sudden cardiac death in persons aged 1–35 years

(2010) Bo Gregers Winkel et al.   EUROPEAN HEART JOURNAL

Hypertrophic cardiomyopathy: from genetics to treatment

(2010) Ali J. Marian   EUROPEAN JOURNAL OF CLINICAL INVESTIGATION

Genetics and cardiac channelopathies

(2010) Oscar Campuzano et al.   GENETICS IN MEDICINE

Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds

(2010) Jonathan R. Skinner et al.   HEART RHYTHM

Genetics of Dilated Cardiomyopathy

(2010) Diane Fatkin et al.   Heart Failure Clinics

Inherited Cardiac Diseases Caused by Mutations in the Nav1.5 Sodium Channel

(2009) JACOB TFELT-HANSEN et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

The QT syndromes: long and short

(2008) Hiroshi Morita et al.   LANCET