(Q82086471)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

title

Three generations of hereditary long-QT syndrome with complete penetrance caused by the p.G316E KCNQ1 mutation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

author name string

M Teresa Viadero

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Esther Rubín

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Teresa Amigo

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Domingo González-Lamuño

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

publication date

28 October 2010

1 reference

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14 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

volume

32

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

page(s)

102-104

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20981542%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00246-010-9821-7

14 January 2020

exact match

0 references

1 reference

12 December 2020

Risk of cardiac events in family members of patients with long QT syndrome.

1 reference

12 December 2020

ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the ACC/AHA/NASPE 2002 Gui

1 reference

12 December 2020

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

1 reference

12 December 2020

ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiolo

1 reference

12 December 2020

Measurement of the QT interval and the risk associated with QTc interval prolongation: a review

1 reference

12 December 2020

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

1 reference

12 December 2020

Compound mutations: a common cause of severe long-QT syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

1 reference

12 December 2020

Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome

1 reference

12 December 2020

Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.

1 reference

12 December 2020

Diagnostic criteria for the long QT syndrome. An update

1 reference

12 December 2020

The long QT syndromes: a critical review, new clinical observations and a unifying hypothesis

1 reference

12 December 2020