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Alström syndrome, arrhythmia, cardiomyopathy.
Anderson-Fabry, heart failure, renal failure, stroke, genetics, enzyme replacement therapy.
European Society of Cardiology (ESC)
Gaucher disease, heart in Gaucher disease, genetics of Gaucher disease, lysosomal disease.
atrium, cardiac surgery, haematopoietic progenitor cells, myxoma, trisomy.
cardiomyopathies, arrhythmia syndromes, splice mutations, molecular diagnosis.
congestive heart failure
education, cardiogenetics, endurance exercise, cardiovascular benefits.
idiopathic restrictive cardiomyopathy, hypertrophic cardiomyopathy, sarcomeric genes.
idiopathic ventricular fibrillation, cardiac arrest, gene mutation, Brugada syndrome.
lysosomal storage disorders, diagnosis and management.
mucopolysaccharidoses (MPS), heart, heart and MPS, genetics and MPS.
myocardial and pericardial diseases
sequence capture, massively parallel sequencing, restrictive cardiomyopathy, desmin, missense mutation.
sudden cardiac death
Marino, Bruno, Pediatric Cardiology, Department of Pediatrics La Sapienza University, Rome, Italy
Vol 1, No 1 (2011)
- Letters to the Editor
22q11.2 deletion (DiGeorge) syndrome: a mother’s open letter
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