Alzheimer's Disease & Dementia
Transthyretin-associated Familial Amyloid Polyneuropathy—Current and Emerging Therapies
Mario Nuvolone, Laura Obici, Giampaolo Merlini
Amyloidoses encompass a heterogeneous group of disorders characterised by the accumulation and extracellular deposition of insoluble aggregates of misfolded fibrillar proteins termed amyloid, which can lead to tissue damage and organ dysfunction.1 They can be exceptionally rare or rather frequent, acquired or hereditary, localised or systemic, quite indolent or life-threatening. Amyloidoses are classified based on […]