Article
Tolcapone, a potent aggregation inhibitor for the treatment of familial leptomeningeal amyloidosis.
The FEBS journal - 1 Jan 2021
Pinheiro Francisca, Varejão Nathalia, Esperante Sebastian, Santos Jaime, Velázquez-Campoy Adrián, Reverter David, Pallarès Irantzu, Ventura Salvador
Abstract excerpt
Hereditary transthyretin amyloidosis (ATTR) is a disease characterized by the extracellular deposition of transthyretin (TTR) amyloid fibrils. Highly destabilizing TTR mutations cause leptomeningeal amyloidosis, a rare, but fatal, disorder in which TTR aggregates in the brain. The disease remains intractable, since liver transplantation, the reference therapy for systemic ATTR, does not stop mutant TTR production...
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