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Article

Intravenous nimodipine worsening prolonged attack of familial hemiplegic migraine.

The journal of headache and pain - 1 Dec 2008

Mjåset Christer, Russell Michael Bjørn

Abstract excerpt

We present a Norwegian family with familial hemiplegic migraine (FHM) with possibly four affected in three generations. The family had a point mutation in the ATP1A2 gene that caused a change of the amino acid valine to methionine (V628 M). The symptoms were pure FHM with intra- and interindividual variability, and epilepsy is not part of the clinical picture. Attacks could be provoked by physical activity. The...

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Source

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Identifiers

PMID: 18846413
DOI: 10.1007/s10194-008-0074-2
PMCID: PMC3452075

Provenance

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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