Amyloidosis is a disease caused by pathological fibril aggregation and deposition of
proteins in different tissues and organs. Thirty-six fibril-forming proteins have been identified …

Localized gastric amyloidosis (LGA) is a rare disease characterized by abnormal
extracellular deposition of amyloid protein restricted to the stomach and it is confirmed by …

Cardiac ATTR amyloidosis, a serious but much under-diagnosed form of cardiomyopathy, is
caused by deposition of amyloid fibrils derived from the plasma protein transthyretin (TTR) …

The tissue diagnosis of amyloidosis and confirmation of fibril protein type, which are crucial
for clinical management, have traditionally relied on Congo red (CR) staining followed by …

In the last decades, the decellularization (DC) of organs has become an established
technique in the field of regenerative medicine to yield complex and vascularized …

Background Antibody-mediated rejection (AMR) accounts for> 50% of kidney allograft loss.
Donor-specific antibodies (DSA) against HLA and non-HLA antigens in the glomeruli and …

Systemic amyloidosis is a serious disease which is caused when normal circulating proteins
misfold and aggregate extracellularly as insoluble fibrillary deposits throughout the body …

Apolipoprotein A‐IV amyloidosis is an uncommon form of the disease normally resulting in
renal and cardiac dysfunction. ApoA‐IV amyloidosis was identified in 16 patients attending …

Introduction Hereditary fibrinogen Aα-chain (AFib) amyloidosis is a relatively uncommon
renal disease associated with a small number of pathogenic fibrinogen Aα (FibA) variants; …

Background Reliable typing of amyloid is essential. Amyloid extraction from tissue enables
immunochemical typing of the precursor protein using an enzyme-linked immunosorbent …