(Q33164590)

English

A novel cardiac ryanodine receptor gene (RyR2) mutation in an athlete with aborted sudden cardiac death: a case of adult-onset catecholaminergic polymorphic ventricular tachycardia

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

A novel cardiac ryanodine receptor gene (RyR2) mutation in an athlete with aborted sudden cardiac death: a case of adult-onset catecholaminergic polymorphic ventricular tachycardia (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

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catecholaminergic polymorphic ventricular tachycardia

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ventricular tachycardia

1 reference

based on heuristic

inferred from title

author name string

Junko Arakawa

1

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Akira Hamabe

2

1 reference

Europe PubMed Central

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23 July 2017

Takeshi Aiba

3

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Tomoo Nagai

4

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Mikoto Yoshida

5

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Takumi Touya

6

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Norio Ishigami

7

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Hideki Hisadome

8

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Shuichi Katsushika

9

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Hirotsugu Tabata

10

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Yoshihiro Miyamoto

11

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Wataru Shimizu

12

1 reference

Europe PubMed Central

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23 July 2017

publication date

5 August 2014

1 reference

Europe PubMed Central

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23 July 2017

Heart and Vessels

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Europe PubMed Central

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23 July 2017

30

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Europe PubMed Central

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23 July 2017

6

1 reference

Europe PubMed Central

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23 July 2017

835-840

1 reference

Europe PubMed Central

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23 July 2017

Current perspectives in genetic cardiovascular disorders: from basic to clinical aspects

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading [...]

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

A novel ryanodine receptor mutation linked to sudden death increases sensitivity to cytosolic calcium.

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Ryanodine receptor-mediated arrhythmias and sudden cardiac death.

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

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

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Guidelines for Non-Pharmacotherapy of Cardiac Arrhythmias (JCS 2011).

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

The clinical management of relatives of young sudden unexplained death victims; implantable defibrillators are rarely indicated.

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Correlation of clinical, endocrine and molecular abnormalities with in vivo responses to high-dose testosterone in patients with partial androgen insensitivity syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

In situ confocal imaging in intact heart reveals stress-induced Ca(2+) release variability in a murine catecholaminergic polymorphic ventricular tachycardia model of type 2 ryanodine receptor(R4496C+/-) mutation

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Genetic characterization of familial CPVT after 30 years.

1 reference

https://api.crossref.org/works/10.1007%2FS00380-014-0555-Y

21 January 2018

Recommendations and considerations related to preparticipation screening for cardiovascular abnormalities in competitive athletes: 2007 update: a scientific statement from the American Heart Association Council on Nutrition, Physical Activity, and M

1 reference

https://pubmed.ncbi.nlm.nih.gov/25092222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical characteristics of sudden cardiac arrest in asymptomatic patients with congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/25092222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Are there juvenile and adult types in patients with catecholaminergic polymorphic ventricular tachycardia?

1 reference

https://pubmed.ncbi.nlm.nih.gov/25092222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ryanodine receptor (RyR2) mutations in sudden cardiac death: studies in extended pedigrees and phenotypic characterization in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/25092222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype variability in patients carrying KCNJ2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/25092222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk stratification for prevention of sudden cardiac death

1 reference

https://pubmed.ncbi.nlm.nih.gov/25092222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/25092222

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00380-014-0555-Y

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

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