(Q46634056)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

title

Magnetic resonance investigations in Brugada syndrome reveal unexpectedly high rate of structural abnormalities (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

1 reference

9

1 reference

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1 February 2020

Carlo Napolitano

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

author name string

Oronzo Catalano

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Serena Antonaci

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Guido Moro

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Maria Mussida

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Mauro Frascaroli

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Maurizia Baldi

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Franco Cobelli

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Paola Baiardi

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Raffaella Bloise

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Nicola Monteforte

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

Silvia G Priori

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

publication date

26 June 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

1 February 2020

published in

European Heart Journal

1 reference

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1 February 2020

volume

30

1 reference

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1 February 2020

issue

18

1 reference

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1 February 2020

page(s)

2241-2248

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19561025%20AND%20SRC:MED&resulttype=core&format=json

Proposed diagnostic criteria for the Brugada syndrome

1 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Brugada syndrome: from cell to bedside

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

The Brugada syndrome: ionic basis and arrhythmia mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Natural history of Brugada syndrome: insights for risk stratification and management

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

The cardiac sodium channel: gating function and molecular pharmacology

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Genetic control of sodium channel function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Ventricular fibrillation without apparent heart disease: description of six cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Right bundle branch block, right precordial st-segment elevation, and sudden death in young people.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Abnormal response to sodium channel blockers in patients with Brugada syndrome: augmented localised wall motion abnormalities in the right ventricular outflow tract region detected by electron beam computed tomography

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Magnetic resonance imaging findings in patients with Brugada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Role of cardiovascular magnetic resonance imaging in arrhythmogenic right ventricular dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Agreement between methods of measurement with multiple observations per individual.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHP252