Brugada Syndrome
Brugada Syndrome - April 24, 2015
What is Brugada syndrome?
NIH Genetics Home Reference
Brugada syndrome![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
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
Brugada syndrome: clinical and genetic findings.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
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.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
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.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
Sieira J et al. Circ Arrhythm Electrophysiol 2015 Apr 22.
Sieira J et al. Circ Arrhythm Electrophysiol 2015 Apr 22.
Sudden cardiac death.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
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 history and phenotype-genotype correlation in pediatric Brugada syndrome: More burden to bear in clinical and genetic diagnosis.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
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.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
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.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
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.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
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.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
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.![External Web Site Icon External Web Site Icon](https://lh3.googleusercontent.com/blogger_img_proxy/AEn0k_sTOQXSz98DkiVr599EHle6XoRFsNJKsms-6eK7JZXK2xMEh4thMlRSTLMSBlaucQCBeW87KGynLIASkyNRbuxjTv3aussFzSE6feLWtJAJ_GJDNzJ-NJ1W=s0-d)
Campuzano O et al. PLoS ONE 2014 (12) e114894
Campuzano O et al. PLoS ONE 2014 (12) e114894
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