Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference26 articles.
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2. Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective;Rapezzi;Eur Heart J,2013
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4. Genotype and phenotype of transthyretin cardiac amyloidosis: THAOS (transthyretin amyloid outcome survey);Maurer;J Am Coll Cardiol,2016
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1. Patisiran, an RNAi therapeutic for hereditary transthyretin-mediated amyloidosis: Sub-analysis in Taiwanese patients from the APOLLO study;Journal of the Formosan Medical Association;2024-09
2. Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study;Orphanet Journal of Rare Diseases;2023-09-13
3. Efficacy of Tafamidis in Patients with Ala97Ser Hereditary Transthyretin Cardiac Amyloidosis: A Six-Month Follow-Up Study;ACTA CARDIOL SIN;2023
4. The Hidden Heart Disease: Shedding Light on Cardiac Amyloidosis;ACTA CARDIOL SIN;2023
5. 2023 Expert Consensus of the Taiwan Society of Cardiology on the Diagnosis and Treatment of Cardiac Amyloidosis;ACTA CARDIOL SIN;2023
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