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Article

Hereditary ATTR amyloidosis: a single-institution experience with 266 patients.

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis - 1 Jan 2015

Swiecicki Paul L, Zhen David B, Mauermann Michelle L, Kyle Robert A, Zeldenrust Steven R, Grogan Martha, Dispenzieri Angela, Gertz Morie A

Abstract excerpt

BACKGROUND: Hereditary transthyretin amyloidosis (ATTR amyloidosis) is a rare, clinically heterogeneous disease due to heritable mutations that lead to misfolding of a precursor protein and multisystem disease. This study sought to define the clinical characteristics, distribution of mutations and phenotypic presentation of patients presenting to our center with hereditary ATTR amyloidosis. METHODS: With...

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Identifiers

PMID: 26017327
DOI: 10.3109/13506129.2015.1019610

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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