The deterioration of skeletal muscle with advancing age has long been anecdotally
recognized and has been of scientific interest for more than 150 years. Over the past several …

Background and aims. Hereditary transthyretin amyloidosis with polyneuropathy (ATTRv) is
caused by mutations in the TTR gene, leading to misfolded monomers that aggregate …

El estudio de la composición corporal humana ha cobrado una relevancia creciente en las
últimas décadas, debido a sus enormes aplicaciones en los terrenos clínico, deportivo y de …

Purpose Hereditary transthyretin amyloidosis with polyneuropathy (ATTRv) is caused by
mutations in the TTR gene, leading to misfolded monomers that aggregate generating …

Hereditary transthyretin amyloidosis (hATTR) is a life-threatening multisystemic disease with
sensory-motor peripheral neuropathy, cardiomyopathy and dysautonomia. Although the six …

Amyloidosis refers to a group of rare but potentially fatal, protein misfolding diseases. The
heart is frequently involved in the most common types, that is, immunoglobulin light chain …

Background Familial amyloidosis polyneuropathy (FAP) is a rare, progressive, and life-
threatening disease inherited in the autosomal dominant pattern. Liver transplantation is the …

Abstract Background Apo A‐I Leu75Pro amyloidosis is a rare systemic hereditary disease,
whose hallmark and earliest involvement is testicular impairment, characterized by …

Amyloidosis is a rare, systemic disease that can result in significant functional impairment.
Specific guidelines for the rehabilitation assessment of amyloidosis patients have yet to be …

Background: In transthyretin amyloid cardiomyopathy (ATTR-CM), the assessment of
functional capacity is of great importance. A distance< 300m covered in the 6-minute walk …