Intravenous nimodipine worsening prolonged attack of familial hemiplegic migraine
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...
| Main Authors: | , |
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| Format: | Online |
| Language: | English |
| Published: |
Springer Milan
2008
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3452075/ |