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Transthyretin cardiac amyloidosis in continental Western Europe: an insight through the Transthyretin Amyloidosis Outcomes Survey (THAOS)

AbstractAims. Transthyretin amyloidosis (ATTR amyloidosis) is a heterogeneous disorder with cardiac, neurologic, and mixed phenotypes. We describe the phenotyp

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Bibliographische Detailangaben
Hauptverfasser: Damy, Thibaud (VerfasserIn) , Kristen, Arnt (VerfasserIn) , Suhr, Ole B. (VerfasserIn) , Maurer, Mathew S. (VerfasserIn) , Planté-Bordeneuve, Violaine (VerfasserIn) , Yu, Ching-Ray (VerfasserIn) , Ong, Moh-Lim (VerfasserIn) , Coelho, Teresa (VerfasserIn) , Rapezzi, Claudio (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2022
In: European heart journal
Year: 2022, Jahrgang: 43, Heft: 5, Pages: 391-400
ISSN:1522-9645
DOI:10.1093/eurheartj/ehz173
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1093/eurheartj/ehz173
Verlag, lizenzpflichtig, Volltext: https://academic.oup.com/eurheartj/advance-article/doi/10.1093/eurheartj/ehz173/5425268
Volltext
Verfasserangaben:Thibaud Damy, Arnt V. Kristen, Ole B. Suhr, Mathew S. Maurer, Violaine Planté-Bordeneuve, Ching-Ray Yu, Moh-Lim Ong, Teresa Coelho, Claudio Rapezzi

MARC

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