+ Site Statistics
+ Search Articles
+ PDF Full Text Service
How our service works
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ Translate
+ Recently Requested

Phenotype (ECG)-genotype considerations in long QT syndrome and Brugada syndrome

Phenotype (ECG)-genotype considerations in long QT syndrome and Brugada syndrome

Journal of Cardiovascular Electrophysiology 11(9): 1055-1057

Please choose payment method:

(PDF emailed within 0-6 h: $19.90)

Accession: 046973614

Download citation: RISBibTeXText

PMID: 11021477

DOI: 10.1111/j.1540-8167.2000.tb00179.x

Related references

Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants. Heart Rhythm 15(7): 1051-1057, 2018

Genotype-phenotype correlations in Brugada syndrome. Journal of Electrocardiology 38(4-Supp-S): 74-0, 2005

SCN5A mutations associated with overlap phenotype of long QT syndrome type 3 and Brugada syndrome. Circulation Journal 78(5): 1061-1062, 2014

Specific therapy based on the genotype and cellular mechanism in inherited cardiac arrhythmias. Long QT syndrome and Brugada syndrome. Current Pharmaceutical Design 11(12): 1561-1572, 2005

Specific Therapy Based on the Genotype and Cellular Mechanism in Inherited Cardiac Arrhythmias. Long Qt Syndrome and Brugada Syndrome. Current Pharmaceutical Design 11(12): 1561-1572, 2005

Brugada syndrome: in search of a genotype-phenotype relationship. Herzschrittmachertherapie and Elektrophysiologie 13(3): 142-148, 2002

Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect. Journal of the American Heart Association 5(7):, 2016

Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome. Circulation. Arrhythmia and Electrophysiology 6(5): 946-951, 2013

Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry. Circulation 121(5): 635-643, 2010

Genotype-phenotype correlation in tissue models of Brugada syndrome simulating patients with sodium and calcium channelopathies. Heart Rhythm 7(6): 820-827, 2010

Long QT syndrome Genotype-phenotype relationship and relation to sudden infant death syndrome. American Journal of Human Genetics 65(4): A289, 1999

The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome. Heart 78(2): 110-116, 1997

Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry. Circulation 135(23): 2255-2270, 2017

Absence of family history and phenotype-genotype correlation in pediatric Brugada syndrome: more burden to bear in clinical and genetic diagnosis. Pediatric Cardiology 36(5): 1090-1096, 2015

Reappraisal of the Worldwide Prevalence of Brugada Syndrome and Brugada Phenotype: From the Old to the New Diagnostic Criteria. Acta Cardiologica Sinica 34(3): 278-279, 2018