Counseling Family Members and Monitoring for Evidence of Disease in Asymptomatic Carriers of Amyloid Transthyretin Cardiac Amyloidosis

Author:

Barker Naomi,Judge Daniel P.ORCID

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference43 articles.

1. Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective;Rapezzi;Eur Heart J,2013

2. The molecular biology and clinical features of amyloid neuropathy;Benson;Muscle Nerve,2007

3. Guideline of transthyretin-related hereditary amyloidosis for clinicians;Ando;Orphanet J Rare Dis,2013

4. Transthyretin cardiac amyloidosis: a treatable form of heart failure with a preserved ejection fraction;Griffin;Trends Cardiovasc Med,2021

5. Rowczenio D, Wechalekar A. Mutations in hereditary amyloidosis. Available at: http://amyloidosismutations.com. Accessed on February 2, 2022.

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