Practical recommendations for the diagnosis and management of transthyretin cardiac amyloidosis

Cardiac amyloidosis (CA) is an infiltrative restrictive cardiomyopathy caused by accumulation in the heart interstitium of amyloid fibrils formed by misfolded proteins. Most common CA types are light chain amyloidosis (AL) caused by monoclonal immunoglobulin light chains and transthyretin amyloidosi...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Heart failure reviews 2021-07, Vol.26 (4), p.861-879
Hauptverfasser:	Bistola, Vasiliki, Parissis, John, Foukarakis, Emmanouil, Valsamaki, Pipitsa N., Anastasakis, Aris, Koutsis, Georgios, Efthimiadis, Georgios, Kastritis, Efstathios
Format:	Artikel
Sprache:	eng
Schlagworte:	Amyloidosis Aortic stenosis Biopsy Cardiology Cardiomyopathy Congestive heart failure Diagnosis Disease Dyspnea Fibrils Heart failure Hospitals Hypertension Hypertrophy Immunoglobulins Light chains Magnetic resonance imaging Medical prognosis Medicine Medicine & Public Health Mutation Pacemakers Protein folding Proteins Rare diseases Scintigraphy Stenosis Transthyretin Ventricle
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!