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Cardiac Amyloidosis: A Narrative Review of Diagnostic Advances and Emerging Therapies

Cardiac Amyloidosis: A Narrative Review of Diagnostic Advances and Emerging Therapies

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_12109326

Cardiac Amyloidosis: A Narrative Review of Diagnostic Advances and Emerging Therapies

About this item

Full title

Cardiac Amyloidosis: A Narrative Review of Diagnostic Advances and Emerging Therapies

Publisher

Switzerland: MDPI AG

Journal title

Biomedicines, 2025-05, Vol.13 (5), p.1230

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

Background/Objectives: Cardiac amyloidosis (CA) is an underdiagnosed and potentially life-threatening infiltrative cardiomyopathy characterized by the extracellular deposition of misfolded amyloid fibrils in cardiac tissue. It is most commonly associated with light-chain (AL) amyloidosis and transthyretin (ATTR) amyloidosis, either hereditary or wi...

Alternative Titles

Full title

Cardiac Amyloidosis: A Narrative Review of Diagnostic Advances and Emerging Therapies

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_12109326

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_12109326

Other Identifiers

ISSN

2227-9059

E-ISSN

2227-9059

DOI

10.3390/biomedicines13051230

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