Cargando…
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...
| Autores principales: | , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Milan
2008
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3452075/ https://www.ncbi.nlm.nih.gov/pubmed/18846413 http://dx.doi.org/10.1007/s10194-008-0074-2 |