Getting to the heart of the matter: cardiac involvement in transthyretin-related amyloidosis
Author:
Publisher
Oxford University Press (OUP)
Subject
Cardiology and Cardiovascular Medicine
Link
http://academic.oup.com/eurheartj/article-pdf/34/7/483/17897464/ehs238.pdf
Reference10 articles.
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2. Amyloid fibril protein nomenclature—2002;Westermark;Amyloid,2002
3. Transthyretin-related familial amyloidotic polyneuropathy—progress in Kumamoto, Japan (1967–2010);Araki;Proc Jap Acad Ser B Phys Biol Sci Nippon Gakushiin,2010
4. Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective;Rapezzi;Eur Heart J,2013
5. Serum cardiac troponins and N-terminal pro-brain natriuretic peptide: a staging system for primary systemic amyloidosis;Dispenzieri;J Clin Oncol,2004
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2. Oral Therapy for the Treatment of Transthyretin-Related Amyloid Cardiomyopathy;International Journal of Molecular Sciences;2022-12-18
3. Early transverse tubule involvement in cardiomyocytes in hereditary transthyretin amyloidosis: a possible cause of cardiac events;Cardiovascular Pathology;2022-11
4. Frequency of and Prognostic Significance of Cardiac Involvement at Presentation in Hereditary Transthyretin-Derived Amyloidosis and the Value of N-Terminal Pro-B-Type Natriuretic Peptide;The American Journal of Cardiology;2018-01
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