(Q74603942)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9608799%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

review article

1 reference

title

[Genetic bases of arrhythmias] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9608799%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1

R Brugada

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9608799%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

publication date

1 April 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9608799%20AND%20SRC:MED&resulttype=core&format=json

Revista Española de Cardiología

12 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9608799%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

volume

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9608799%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9608799%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

page(s)

274-285

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9608799%20AND%20SRC:MED&resulttype=core&format=json

Familial symptomatic sinus bradycardia: autosomal dominant inheritance

12 November 2019

cites work

1 reference

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7 January 2021

A Case of Familial Ventricular Tachycardia

1 reference

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7 January 2021

Familial occurrence of accessory atrioventricular pathways (preexcitation syndrome).

1 reference

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7 January 2021

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

1 reference

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7 January 2021

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Cardiomyopathy in the Kearns-Sayre syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

1 reference

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7 January 2021

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Sudden death in young competitive athletes. Clinical, demographic, and pathological profiles.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Causes of sudden death in competitive athletes

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Sudden cardiac death in hypertrophic cardiomyopathy. Variability in phenotypic expression of beta-myosin heavy chain mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1)

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Prognosis in hypertrophic cardiomyopathy: role of age and clinical, electrocardiographic and hemodynamic features

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Prognostic significance of 24 hour ambulatory electrocardiographic monitoring in patients with hypertrophic cardiomyopathy: a prospective study

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Myocardial ischemia detected by thallium scintigraphy is frequently related to cardiac arrest and syncope in young patients with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Arrhythmogenic right ventricular dysplasia/cardiomyopathy: a review.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

An isolated cardiac conduction disease maps to chromosome 19q

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Atrial fibrillation: a major contributor to stroke in the elderly. The Framingham Study

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Identification of a genetic locus for familial atrial fibrillation

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

The long QT syndrome. Prospective longitudinal study of 328 families

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Exclusion of HRAS from long QT locus

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Multiple mechanisms of Na+ channel--linked long-QT syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

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/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-8932%2898%2974745-1

7 January 2021

10.1016/S0300-8932(98)74745-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9608799%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference