Channelopathies: Brugada syndrome, long QT syndrome, short QT syndrome, and CPVT
R Schimpf, C Veltmann, C Wolpert, M Borggrefe - Herz, 2009 - search.proquest.com
Abstract In approximately 10-20% of all sudden deaths, no structural cardiac abnormalities
can be identified. Important potential causes of sudden cardiac deaths in the absence of …
can be identified. Important potential causes of sudden cardiac deaths in the absence of …
Ion channel diseases: an update for 2016
GF Tomaselli, AS Barth - Current treatment options in cardiovascular …, 2016 - Springer
Opinion statement Ion channelopathies are a frequent cause of sudden cardiac death (SCD)
in patients with structurally normal hearts. These are generally Mendelian inherited electrical …
in patients with structurally normal hearts. These are generally Mendelian inherited electrical …
Genetic testing for cardiac channelopathies: ten questions regarding clinical considerations for heart rhythm allied professionals
DJ Tester, MJ Ackerman - Heart Rhythm, 2005 - heartrhythmjournal.com
The study of cardiac channelopathies represents a relatively new discipline among heart
rhythm specialists and allied professionals. In 1995, the discipline of cardiac …
rhythm specialists and allied professionals. In 1995, the discipline of cardiac …
Sudden cardiac death: what is inside our genes?
A Sarkozy, P Brugada - The Canadian journal of …, 2005 - pubmed.ncbi.nlm.nih.gov
Although sudden cardiac death in youths is generally rare, it is estimated that 10% to 20% of
these deaths occur in previously healthy infants, children, adolescents and young adults …
these deaths occur in previously healthy infants, children, adolescents and young adults …
Cardiac channelopathies: recognition, treatment, management
KT Hickey, A Elzomor - AACN Advanced Critical Care, 2018 - AACN
The discovery of the human genome has ushered in a new era of molecular testing,
advancing our knowledge and ability to identify cardiac channelopathies. Genetic variations …
advancing our knowledge and ability to identify cardiac channelopathies. Genetic variations …
Genetics of ion-channel disorders
M Cerrone, C Napolitano, SG Priori - Current opinion in cardiology, 2012 - journals.lww.com
Over a few years, the field of inherited arrhythmogenic diseases has rapidly expanded, thus
reshaping clinical management for these conditions. It is now clear that to handle these …
reshaping clinical management for these conditions. It is now clear that to handle these …
Genetics of arrhythmia: disease pathways beyond ion channels
Diseases of the electrical conduction system that lead to irregularities in cardiac rhythm can
have morbid and often lethal clinical outcomes. Linkage analysis has been the principal tool …
have morbid and often lethal clinical outcomes. Linkage analysis has been the principal tool …
Cardiac channelopathies: diagnosis and contemporary management
The inherited arrhythmia (IA) syndromes are a group of disorders characterised by an
increased risk of sudden cardiac death (SCD), abnormal cardiac electrical function and …
increased risk of sudden cardiac death (SCD), abnormal cardiac electrical function and …
Molecular mechanisms of inherited arrhythmias
CM Wolf, CI Berul - Current genomics, 2008 - ingentaconnect.com
Inherited arrhythmias and conduction system diseases are known causes of sudden cardiac
death and are responsible for significant mortality and morbidity in patients with congenital …
death and are responsible for significant mortality and morbidity in patients with congenital …
Inherited arrhythmia syndromes
AAM Wilde, HL Tan - Circulation Journal, 2007 - jstage.jst.go.jp
Inherited cardiac arrhythmia syndromes have received a lot of attention in recent years,
particularly the molecular genetic basis, which has been unraveled to a great extent in the …
particularly the molecular genetic basis, which has been unraveled to a great extent in the …