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Alström syndrome, arrhythmia, cardiomyopathy.
Brugada syndrome, arrhythmia, genetics, double mutant, sodium channel.
atrium, cardiac surgery, haematopoietic progenitor cells, myxoma, trisomy.
cardiomyopathies, arrhythmia syndromes, splice mutations, molecular diagnosis.
echocardiography, Fabry disease, cardiomyopathy.
education, cardiogenetics, endurance exercise, cardiovascular benefits.
education, familial hypertrophic cardiomyopathy phenotype, left ventricular systolic dysfunction, extensive myocardial fibrosis, cardiogenetics.
hypertrophic cardiomyopathy, HCM, gene expression, microarray.
idiopathic restrictive cardiomyopathy, hypertrophic cardiomyopathy, sarcomeric genes.
idiopathic ventricular fibrillation, cardiac arrest, gene mutation, Brugada syndrome.
inherited cardiac disease
sequence capture, massively parallel sequencing, restrictive cardiomyopathy, desmin, missense mutation.
speckle tracking echocardiography, Fabry disease, Friedreich ataxia, amyloidosis.
sudden cardiac death
Goldenberg, Paula, Division of Pediatric Cardiology, The Heart Institute, Cincinnati Children’s Hospital Medical Center, OH, United States
Vol 2, No 1 (2012)
- Brief Reports
Cardiac electrical system involvement in Alström syndrome: uncommon causes of dilated cardiomyopathies
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