Hypertrophic cardiomyopathy (HCM) is a genetic disorder that is characterized by left
ventricular hypertrophy unexplained by secondary causes and a nondilated left ventricle …

Hypertrophic cardiomyopathy (HCM) is a heterogeneous genetic disorder most often caused
by sarcomeric mutations resulting in left ventricular hypertrophy, fibrosis, hypercontractility …

Hypertrophic cardiomyopathy (HCM) is the most-common monogenically inherited form of
heart disease, characterized by thickening of the left ventricular wall, contractile dysfunction …

Endometriosis is associated with chronic inflammation, and reactive oxygen species (ROS)
are proinflammatory mediators that modulate cell proliferation. We have investigated …

Progress in precision medicine is limited by insufficient knowledge of transcriptomic or
proteomic features in involved tissues that define pathobiological differences between …

Hypertrophic cardiomyopathy (HCM) is the most common genetic heart disease, affecting
over one million individuals in Europe. Hypertrophic cardiomyopathy patients often require …

Hypertrophic cardiomyopathy (HCM), the most common inherited heart disease, is still
orphan of a specific drug treatment. The erroneous consideration of HCM as a rare disease …

Hypertrophic cardiomyopathy (HCM) is the most common inherited heart disease and
defined by unexplained isolated progressive myocardial hypertrophy, systolic and diastolic …

As described in earlier reviews in this series on the molecular basis of hypertrophic
cardiomyopathy (HCM), HCM is one of the archetypal monogenic cardiovascular disorders …

The mechanism underlying the development of chronic kidney disease (CKD) after acute
kidney injury (AKI) remains unclear. Maladaptive repair has been considered an important …