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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...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Milan
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3452075/ https://ncbi.nlm.nih.gov/pubmed/18846413 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10194-008-0074-2 |
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