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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.
cardiovascular research, bioinformatic approaches.
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
mitochondrial DNA, respiratory chain deficiency, mitochondrial cardiomyopathy, T3258C, A3243G.
sequence capture, massively parallel sequencing, restrictive cardiomyopathy, desmin, missense mutation.
sudden cardiac death
Limongelli, Giuseppe, Second University of Naples, Monaldi Hospital, Naples, Italy
Vol 1, No 1S (2011): Ion channel diseases: molecular basis, clinical findings, and management
Ion channels and beating heart: the players and the music
Vol 1, No 1 (2011)
A new era in cardiogenetics
Vol 3, No 1 (2013)
Imaging in Rare Disease: a roadmap for diagnosis
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