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Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update

Transthyretin amyloidosis (ATTR amyloidosis) is a rare, life-threatening disease caused by the accumulation of variant or wild-type (ATTRwt amyloidosis) transthyretin amyloid fibrils in the heart, peripheral nerves, and other tissues and organs.

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Hauptverfasser: Dispenzieri, Angela (Verfasst von) , Coelho, Teresa (Verfasst von) , Conceição, Isabel (Verfasst von) , Waddington-Cruz, Márcia (Verfasst von) , Wixner, Jonas (Verfasst von) , Kristen, Arnt (Verfasst von) , Rapezzi, Claudio (Verfasst von) , Planté-Bordeneuve, Violaine (Verfasst von) , Gonzalez-Moreno, Juan (Verfasst von) , Maurer, Mathew S. (Verfasst von) , Grogan, Martha (Verfasst von) , Chapman, Doug (Verfasst von) , Amass, Leslie (Verfasst von)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 18 June 2022
In: Orphanet journal of rare diseases
Year: 2022, Jahrgang: 17, Pages: 1-12
ISSN:1750-1172
DOI:10.1186/s13023-022-02359-w
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1186/s13023-022-02359-w
Volltext
Verfasserangaben:Angela Dispenzieri, Teresa Coelho, Isabel Conceição, Márcia Waddington-Cruz, Jonas Wixner, Arnt V. Kristen, Claudio Rapezzi, Violaine Planté-Bordeneuve, Juan Gonzalez-Moreno, Mathew S. Maurer, Martha Grogan, Doug Chapman and Leslie Amass on behalf of the THAOS investigators

MARC

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