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Article

Natural course of Finnish gelsolin amyloidosis.

Annals of medicine - 1 Jan 2015

Nikoskinen Tuuli, Schmidt Eeva-Kaisa, Strbian Daniel, Kiuru-Enari Sari, Atula Sari

Abstract excerpt

BACKGROUND: Finnish type of hereditary gelsolin amyloidosis (FGA) is one of the most common diseases of Finnish disease heritage. Existing FGA knowledge is based only on smaller patient series, so our aim was to elucidate the natural course of the disease in a comprehensive sample of patients and to build up a national FGA patient registry. METHODS: An inquiry about the known and suspected signs of FGA, sent to...

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Share to Amyloidosis
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Corneal Dystrophies, Hereditary

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Source

Identifiers

PMID: 26339870
DOI: 10.3109/07853890.2015.1075063

Genes

FGA

Provenance

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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