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Musculoskeletal co‐morbidities in patients with transthyretin amyloid cardiomyopathy: a systematic review

Abstract The prevalence of transthyretin‐associated amyloidosis cardiomyopathy (ATTR‐CM) has grown because of newer non‐invasive diagnosis tools. Detecting the presence of extra‐cardiac ATTR manifestations such as musculoskeletal pathologies considered ‘red flags’, when there is minimal or non‐cardi...

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Bibliográfalaš dieđut
Váldodahkkit: Francesc Formiga, Laia Saumell Baeza, David Chivite, Sergi Yun
Materiálatiipa: Artigo
Giella:Inglês
Almmustuhtton: Oxford University Press 2024-04-01
Ráidu:ESC Heart Failure
Fáttát:
Liŋkkat:https://doi.org/10.1002/ehf2.14622
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