Coronary and congenital heart malformations contribute to and overlap with clinical
cardiomyopathy. As cellular mechanisms and gene associations are better understood …

INTRODUZIONE: Solo nel 50% dei casi di cardiomiopatia dilatativa (CMD) è possibile
individuare un'eziologia specifica. Nei rimanenti casi è sempre più possibile identificare una …

In recent years, outstanding progress has been made in the diagnosis and treatment of
cardiomyopathies. Genetics is emerging as a primary point in the diagnosis and …

In last 15 years, cardiology has experienced an amazing progress in genetics and molecular
biology. These advances help to develop new methods of prevention, diagnosis and clinical …

Hereditäre Arrhythmiesyndrome mit struktureller Herzerkrankung sind selten. Oft sind relativ
junge, ansonsten gesunde Patienten ohne kardiovaskuläre Risikofaktoren betroffen …

Dilated cardiomyopathy (DCM) is a primary myocardial disease characterized by
progressive systolic dysfunction due to cardiac chamber dilatation and inefficient myocardial …

Background–Today mutations in more than 30 different genes have been found to cause
inherited cardiomyopathies, some associated with very poor prognosis. However, due to the …

Цель—в рамках проведения открытой постмаркетинговой национальной
наблюдательной программы ВЫБОР-2 оценить соответствие между рекомендациями …

Epilepsy is the most common serious neurological condition, and it carries a significant risk
of premature mortality that is 2-to 3-fold higher, on average, than the general population [1 …

Although cases are rare, neonatal and paediatric dilated cardiomyopathy (DCM) is a severe
and often lethal disease, in which a genetic factor plays an important role in disease …