Systemic forms of amyloidosis affecting the heart are mostly light-chain (AL) and
transthyretin (ATTR) amyloidoses. The latter is caused by deposition of misfolded …

Fabry disease is an X-linked inherited lysosomal disorder that causes accumulation of
glycosphingolipids in body fluids and tissues, leading to progressive organ damage and …

The new Internet of Things paradigm allows for small devices with sensing, processing and
communication capabilities to be designed, which enable the development of sensors …

Background Screening in subjects with left ventricular hypertrophy (LVH) reveals a high
prevalence of Fabry disease (FD). Often, a diagnosis is uncertain because characteristic …

Abstract Aims Cardiac involvement in Fabry disease (FD) occurs prior to left ventricular
hypertrophy (LVH) and is characterized by low myocardial native T1 with sphingolipid …

Cardiac amyloidosis (CA) is an infiltrative cardiomyopathy caused by extracellular
deposition of amyloid fibrils, mainly derived from transthyretin, either wild-type or hereditary …

Fabry disease is an X-chromosome-linked lysosomal storage disease characterized by a
deficient activity or, in most males, absence of the enzyme α-galactosidase A (a-Gal A) …

Amyloidosis is an infiltrative disease characterized by deposition of amyloid fibrils within the
extracellular tissue of one or multiple organs. Involvement of the heart, cardiac amyloidosis …

The appropriate diagnosis and subtyping of cardiac amyloidosis (CA) is frequently missed or
delayed due to its vague presentation, clinical overlapping, and diagnostic pitfalls. Recent …

Restrictive cardiomyopathy (RCM) is the least common among cardiomyopathies. It can be
idiopathic, familial, or secondary to systematic disorders. Marked increase in left and/or right …