Descreva sintomas, busque uma doença ou conte sua história. Eu pesquiso em 10.468 doenças raras.
Raras pode cometer erros. Não substitui orientação médica profissional.
311 ensaios clínicos encontrados, 134 ativos.
Hereditary Transthyretin Amyloidosis in Austria: Clinical, Genetic, and Demographic Insights from a Nationwide Cohort.
Therapeutic Efficacy and Safety Profile of Eplontersen in Hereditary Transthyretin-Mediated Amyloidosis: A Systematic Review.
A Cautionary Tale: An Instructive Case of Recognising Non-Amyloid Light Chain Renal Amyloidosis.
Natural variants of apolipoprotein A1 L99P and R173P exhibited a high degree of amyloid fibril formation: Implications for high-density lipoprotein functions and disease pathogenesis.
Genetic and Clinical Spectrum of Hereditary Transthyretin Amyloidosis in Brazil.