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Article

[Fatal familial insomnia: clinical, laboratory and pathological features].

Revista de neurologia - 1 Jan 2000

Montagna P

Abstract excerpt

INTRODUCTION: Fatal familial insomnia (FFI) is a hereditary disease caused by prions and characterized by mutations in the gene of the prion protein. Its clinical, neuropathological and biomolecular properties make this a distinctive and worrying disorder. PATIENTS AND METHODS: We studied the clinical and laboratory findings of 14 patients belonging to three Italian and two French families. The genetic analysis...

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PMID: 10637858

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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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