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Article

Causes of death and life span in Finnish gelsolin amyloidosis.

Annals of medicine - 1 Aug 2016

Schmidt Eeva-Kaisa, Atula Sari, Tanskanen Maarit, Nikoskinen Tuuli, Notkola Irma-Leena, Kiuru-Enari Sari

Abstract excerpt

BACKGROUND: Finnish type of hereditary gelsolin amyloidosis (AGel amyloidosis) is an autosomal dominant disorder. Until recently, there has only been little knowledge of fatal complications of the disease and its possible impact on the patients' life span. METHODS: We identified 272 deceased patients based on patient interviews and genealogical data. After collecting their death certificates, we recorded the...

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Identifiers

PMID: 27137880
DOI: 10.1080/07853890.2016.1177197

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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