Transthyretin amyloid cardiomyopathy: from cause to novel treatments. [PDF]
Fontana M +6 more
europepmc +1 more source
Right Atrial Function as a Novel Predictor for New-Onset Atrial Fibrillation in Transthyretin Amyloid Cardiomyopathy. [PDF]
Kuyama N +28 more
europepmc +1 more source
Serum Transthyretin as a Prognostic and Therapeutic Biomarker in Transthyretin Amyloid Cardiomyopathy Patients Treated with Tafamidis. [PDF]
Costantino J +7 more
europepmc +1 more source
Hereditary transthyretin amyloid cardiomyopathy caused by the rare TTR p.Ser43Asn variant in an Asian family: a case report. [PDF]
Song B +8 more
europepmc +1 more source
Prediagnostic Electrocardiographic Abnormalities in Transthyretin Amyloid Cardiomyopathy: A Longitudinal Observational Study. [PDF]
Venkateshvaran A +2 more
europepmc +1 more source
Development of a Predictive Tool in Patients With High Pretest Probability for Transthyretin Amyloid Cardiomyopathy. [PDF]
Chai J +6 more
europepmc +1 more source
Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy [PDF]
Transthyretin amyloid cardiomyopathy is caused by the deposition of transthyretin amyloid fibrils in the myocardium. The deposition occurs when wild-type or variant transthyretin becomes unstable and misfolds. Tafamidis binds to transthyretin, preventing tetramer dissociation and amyloidogenesis.In a multicenter, international, double-blind, placebo ...
Mathew S Maurer +2 more
exaly +8 more sources
Screening for Transthyretin Amyloid Cardiomyopathy in Everyday Practice [PDF]
Transthyretin amyloid cardiomyopathy (ATTR-CM) is a life-threatening, progressive, infiltrative disease caused by the deposition of transthyretin amyloid fibrils in the heart, and can often be overlooked as a common cause of heart failure. Delayed diagnosis due to lack of disease awareness and misdiagnosis results in a poorer prognosis.
Laura Obici +2 more
exaly +10 more sources
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Transthyretin amyloid cardiomyopathy
Medicina Clínica (English Edition), 2021Transthyretin (TTR) cardiac amyloidosis is a severe, progressive, infiltrative disease caused by the deposition of TTR at cardiac level. It may be due to a genetic alteration in its hereditary form (ATTRv) or as a consequence of an age-related degenerative process (ATTRwt). Thanks to advances in imaging techniques and the possibility of achieving a non-
Pablo, Garcia-Pavia +2 more
openaire +4 more sources

