(Q36203067)

12 August 2017

1 reference

title

The molecular basis of cardiac arrhythmias in patients with cardiomyopathy (English)

1 reference

12 August 2017

4

Kalyanam Shivkumar

1 reference

12 August 2017

Sen Ji

1

1 reference

PubMed ID

16036032

12 August 2017

David Cesario

series ordinal

2

1 reference

PubMed ID

16036032

12 August 2017

Miguel Valderrabano

series ordinal

3

1 reference

12 August 2017

1 September 2004

1 reference

Current heart failure reports

12 August 2017

1 reference

12 August 2017

1

1 reference

12 August 2017

3

1 reference

12 August 2017

98-103

1 reference

https://scigraph.springernature.com/pub.10.1007/s11897-004-0018-3

12 August 2017

0 references

cites work

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

1 reference

https://api.crossref.org/works/10.1007%2FS11897-004-0018-3

Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11897-004-0018-3

Images in cardiovascular medicine. Labile repolarization from "cell to bedside".

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11897-004-0018-3

Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11897-004-0018-3

Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11897-004-0018-3

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11897-004-0018-3

Gene for progressive familial heart block type I maps to chromosome 19q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11897-004-0018-3

Ionic mechanism of action potential prolongation in ventricular myocytes from dogs with pacing-induced heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11897-004-0018-3

Beat-to-beat QT interval variability: novel evidence for repolarization lability in ischemic and nonischemic dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11897-004-0018-3

Identification of a gene responsible for familial Wolff-Parkinson-White syndrome

21 January 2018

1 reference

12 December 2020

Sudden death associated with short-QT syndrome linked to mutations in HERG.

1 reference

12 December 2020

The relationships among ventricular arrhythmias, left ventricular dysfunction, and mortality in the 2 years after myocardial infarction

1 reference

12 December 2020

Abnormalities of calcium cycling in the hypertrophied and failing heart

1 reference

12 December 2020

Arrhythmogenesis and contractile dysfunction in heart failure: Roles of sodium-calcium exchange, inward rectifier potassium current, and residual beta-adrenergic responsiveness

1 reference

12 December 2020

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

12 December 2020

Electrophysiological changes in heart failure and their relationship to arrhythmogenesis

1 reference

12 December 2020

Electrophysiological remodeling in hypertrophy and heart failure

1 reference

12 December 2020

Molecular and cellular mechanisms of cardiac arrhythmias

1 reference

12 December 2020

Molecular biology and the prolonged QT syndromes

1 reference

12 December 2020

Sudden cardiac death in the United States, 1989 to 1998.

1 reference

12 December 2020

Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum

1 reference

12 December 2020

Increased vulnerability of the subendocardium to ischaemic injury: an electrophysiological explanation

1 reference

12 December 2020

Right ventricular outflow tract tachycardia due to a somatic cell mutation in G protein subunitalphai2.

1 reference

12 December 2020

Transmural electrophysiological heterogeneities underlying arrhythmogenesis in heart failure

1 reference

12 December 2020

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 reference

12 December 2020

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

12 December 2020

Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II

1 reference

12 December 2020

Structure and function of cardiac potassium channels

1 reference

12 December 2020

Transmural action potential and ionic current remodeling in ventricles of failing canine hearts

1 reference

12 December 2020

Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21

1 reference

12 December 2020

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

12 December 2020

Genetic Heterogeneity in Familial Dilated Cardiomyopathy

1 reference

12 December 2020

The management of hypertrophic cardiomyopathy

1 reference

12 December 2020

Long QT syndromes and torsade de pointes

1 reference

12 December 2020

Progressive familial heart block--two types

1 reference

12 December 2020

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

12 December 2020

George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.

1 reference

12 December 2020

Repolarization abnormalities in cardiomyocytes of dogs with chronic heart failure: role of sustained inward current.

1 reference

12 December 2020

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts

1 reference

12 December 2020

Genetic and molecular basis of cardiac arrhythmias: impact on clinical management part III

1 reference

12 December 2020

L-type Ca2+ channel density and regulation are altered in failing human ventricular myocytes and recover after support with mechanical assist devices

1 reference

12 December 2020

10.1007/S11897-004-0018-3

Identifiers

DOI

1 reference

12 August 2017

1 reference

PubMed ID

16036032