Diagnosis and treatment of cardiac amyloidosis: position statement of the German Cardiac Society (DGK)

Systemic forms of amyloidosis affecting the heart are mostly light-chain (AL) and transthyretin (ATTR) amyloidoses. The latter is caused by deposition of misfolded transthyretin, either in wild-type (ATTRwt) or mutant (ATTRv) conformation. For diagnostics, specific serum biomarkers and modern non-in...

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Publicat a:Clin Res Cardiol
Autors principals: Yilmaz, A., Bauersachs, J., Bengel, F., Büchel, R., Kindermann, I., Klingel, K., Knebel, F., Meder, B., Morbach, C., Nagel, E., Schulze-Bahr, E., aus dem Siepen, F., Frey, N.
Format: Artigo
Idioma:Inglês
Publicat: Springer Berlin Heidelberg 2021
Matèries:
Review
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8055575/
https://ncbi.nlm.nih.gov/pubmed/33459839
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00392-020-01799-3
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