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Article

Ten years of follow-up in a large family with familial hemiplegic migraine type 1: Clinical course and implications for treatment.

Cephalalgia : an international journal of headache - 1 May 2018

Indelicato Elisabetta, Nachbauer Wolfgang, Eigentler Andreas, Donnemiller Evelin, Wagner Michaela, Unterberger Iris, Boesch Sylvia

Abstract excerpt

Background Familial hemiplegic migraine (FHM) is a rare, genetic form of migraine with aura. The severity of the aura imposes an effective prophylaxis that is currently based on standard anti-migraine drugs. To this concern, only short-term reports are currently available. Methods Eight patients from a multigenerational FHM type 1 family harbouring a T666M mutation in the CACNA1A gene were referred to our ataxia...

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Identifiers

PMID: 28856914
DOI: 10.1177/0333102417715229

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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