(Q33151464)

22 July 2017

1 reference

title

Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia (English)

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catecholaminergic polymorphic ventricular tachycardia

22 July 2017

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ventricular tachycardia

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Päivi J Laitinen

1

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22 July 2017

Heikki Swan

2

1 reference

22 July 2017

Kirsi Piippo

3

1 reference

22 July 2017

Matti Viitasalo

4

1 reference

22 July 2017

Lauri Toivonen

5

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22 July 2017

Kimmo Kontula

6

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22 July 2017

language of work or name

English

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publication date

1 January 2004

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22 July 2017

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22 July 2017

volume

36 Suppl 1

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22 July 2017

page(s)

81-86

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Molecular mechanisms of inherited ventricular arrhythmias

22 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

Familial polymorphic ventricular tachycardia--intracellular calcium channel disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

Ca2+ signalling and muscle disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

Enhanced basal activity of a cardiac Ca2+ release channel (ryanodine receptor) mutant associated with ventricular tachycardia and sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

The binding of the RyR2 calcium channel to its gating protein FKBP12.6 is oppositely affected by ARVD2 and VTSIP mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

Cardiac intracellular calcium release channels: role in heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032599

10.1080/17431380410032599

21 January 2018

Identifiers

DOI

1 reference

22 July 2017

1 reference