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The Hidden Heart Disease: Shedding Light on Cardiac Amyloidosis.

作者信息

Tsai Cheng-Hsuan, Lin Yen-Hung, Wu Yen-Wen

机构信息

Division of Cardiology, Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University.

Cardiovascular Center, National Taiwan University Hospital, Taipei.

出版信息

Acta Cardiol Sin. 2023 Jul;39(4):544-545. doi: 10.6515/ACS.202307_39(4).20230526A.

Abstract
摘要

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本文引用的文献

1
Efficacy of Tafamidis in Patients with Ala97Ser Hereditary Transthyretin Cardiac Amyloidosis: A Six-Month Follow-Up Study.
Acta Cardiol Sin. 2023 Jul;39(4):619-627. doi: 10.6515/ACS.202307_39(4).20221116A.
2
2023 Expert Consensus of the Taiwan Society of Cardiology on the Diagnosis and Treatment of Cardiac Amyloidosis.
Acta Cardiol Sin. 2023 Jul;39(4):511-543. doi: 10.6515/ACS.202307_39(4).20230610A.
3
Tafamidis Treatment Decreases Tc-Pyrophosphate Uptake in Patients With Hereditary Ala97Ser Transthyretin Amyloid Cardiomyopathy.
JACC Cardiovasc Imaging. 2023 Jun;16(6):866-867. doi: 10.1016/j.jcmg.2022.12.016. Epub 2023 Feb 8.
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Reverse cardiac remodelling and dysfunction in A97S transthyretin cardiac amyloidosis after tafamidis treatment.
ESC Heart Fail. 2022 Dec;9(6):4335-4339. doi: 10.1002/ehf2.14165. Epub 2022 Sep 20.
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Cardiac Amyloidosis: Evolving Diagnosis and Management: A Scientific Statement From the American Heart Association.
Circulation. 2020 Jul 7;142(1):e7-e22. doi: 10.1161/CIR.0000000000000792. Epub 2020 Jun 1.
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Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser.
J Formos Med Assoc. 2020 Mar;119(3):693-700. doi: 10.1016/j.jfma.2019.08.027. Epub 2019 Sep 11.
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Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review.
J Am Coll Cardiol. 2019 Jun 11;73(22):2872-2891. doi: 10.1016/j.jacc.2019.04.003.
9
Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy.
N Engl J Med. 2018 Sep 13;379(11):1007-1016. doi: 10.1056/NEJMoa1805689. Epub 2018 Aug 27.

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