Transthyretin amyloid cardiomyopathy: from cause to novel treatments. [PDF]
Fontana M +6 more
europepmc +1 more source
Transthyretin amyloid cardiomyopathy : evolution in 2020
La cardiopathie amyloïde à transthyréthine n’est plus considérée comme une pathologie rare dans sa forme sénile. Le traitement par Tafamidis a démontré une amélioration clinique et fonctionnelle des patients. Nous avons recueilli de manière rétrospective, les données cliniques, biologiques et échocardographiques des patients sous TAFAMIDIS inclus dans ...
openaire +1 more source
Usefulness of Regional Longitudinal Strain to Identify Transthyretin Amyloid Cardiomyopathy. [PDF]
Usuku H +18 more
europepmc +1 more source
Acoramidis in transthyretin amyloid cardiomyopathy: expanding evidence from ATTRibute-CM. [PDF]
Sarswat N +12 more
europepmc +1 more source
Population diversity of the genetically determined expression in human tissues and its implications in TTR amyloidosis [PDF]
core +1 more source
Neuropathologic analysis of Tyr69His TTR variant meningovascular amyloidosis with dementia [PDF]
core +1 more source
Concomitant Transthyretin Amyloid Cardiomyopathy in Patients With Multiple Myeloma. [PDF]
Ibrahim M +9 more
europepmc +1 more source
Proteomics Profiling Reveals Circulating Biomarkers and Dysregulated Pathways in Transthyretin Amyloid Cardiomyopathy. [PDF]
Lu R +7 more
europepmc +1 more source
Treatment of transthyretin (TTR) amyloid cardiomyopathy with an antisense oligonucleotide inhibitor of TTR synthesis [PDF]
Ackermann, Elizabeth J +2 more
core +1 more source
Living with Transthyretin amyloid cardiomyopathy from a patient perspective. [PDF]
Bui QM +7 more
europepmc +1 more source

