Brugada and Long QT Syndrome
Brugada Syndrome - August 26, 2015
A systematic review on the cost-effectiveness of genetic and electrocardiogram testing for Long QT syndrome in infants and young adults.
Gonzalez FM et al. Value Health 2015 Jul 18(5) 700-8
Gonzalez FM et al. Value Health 2015 Jul 18(5) 700-8
What is Brugada syndrome? NIH Genetics Home Reference
NIH Genetics Home ReferenceBrugada syndrome
R Brugada et al. Gene Reviews, April 2014
R Brugada et al. Gene Reviews, April 2014
Find out which genetic conditions and tests are associated with Brugada Syndrome, from the NIH Genetic Testing Registry
from the NIH Genetic Testing RegistryBrugada syndrome: clinical and genetic findings.
Sarquella-Brugada G et al. Genet. Med. 2015 Apr 23.
Sarquella-Brugada G et al. Genet. Med. 2015 Apr 23.
Enhanced classification of Brugada syndrome- and Long QT syndrome-associated genetic variants in the SCN5A-encoded Nav1.5 cardiac sodium channel.
Kapplinger JD et al. Circ Cardiovasc Genet 2015 Apr 22.
Kapplinger JD et al. Circ Cardiovasc Genet 2015 Apr 22.
Prognostic value of programmed electrical stimulation in Brugada syndrome: 20 years experience.
Sieira J et al. Circ Arrhythm Electrophysiol 2015 Apr 22.
Sieira J et al. Circ Arrhythm Electrophysiol 2015 Apr 22.
Sudden cardiac death.
Kuriachan VP et al. Curr Probl Cardiol 2015 Apr (4) 133-200
Kuriachan VP et al. Curr Probl Cardiol 2015 Apr (4) 133-200
Absence of family health history and phenotype-genotype correlation in pediatric Brugada syndrome: More burden to bear in clinical and genetic diagnosis.
Daimi H et al. Pediatr Cardiol 2015 Mar 11.
Daimi H et al. Pediatr Cardiol 2015 Mar 11.
Implantable cardioverter-defibrillator therapy in brugada syndrome: a 20-year single-center experience.
Conte G et al. J. Am. Coll. Cardiol. 2015 Mar 10. (9) 879-88
Conte G et al. J. Am. Coll. Cardiol. 2015 Mar 10. (9) 879-88
Cardiac arrhythmias: Diagnosis, symptoms, and treatments.
Fu DG et al. Cell Biochem. Biophys. 2015 Mar 4.
Fu DG et al. Cell Biochem. Biophys. 2015 Mar 4.
Next generation sequencing for molecular confirmation of hereditary sudden cardiac death syndromes.
Márquez MF et al. Arch Cardiol Mex 2015 Jan-Mar (1) 68-72
Márquez MF et al. Arch Cardiol Mex 2015 Jan-Mar (1) 68-72
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Le Scouarnec S et al. Hum. Mol. Genet. 2015 May 15. (10) 2757-63
Le Scouarnec S et al. Hum. Mol. Genet. 2015 May 15. (10) 2757-63
Identification of genetic alterations, as causative genetic defects in Long QT syndrome, Using next generation sequencing technology.
Campuzano O et al. PLoS ONE 2014 (12) e114894
Campuzano O et al. PLoS ONE 2014 (12) e114894
.png)
No hay comentarios:
Publicar un comentario