The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.

@article{Ducros2001TheCS,
  title={The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.},
  author={Anne Ducros and Charlotte D{\'e}nier and Anne Joutel and Michaelle C{\'e}cillon and Christelle Lescoat and Katayoun Vahedi and Françoise Darcel and {\'E}ric Vicaut and Marie Germaine Bousser and Elisabeth Tournier-Lasserve},
  journal={The New England journal of medicine},
  year={2001},
  volume={345 1},
  pages={
          17-24
        }
}
BACKGROUND Familial hemiplegic migraine, an autosomal dominant disorder characterized by attacks of transient hemiparesis followed by a migraine headache, is classically divided into pure familial hemiplegic migraine (affecting 80 percent of families) and familial hemiplegic migraine with permanent cerebellar signs (affecting 20 percent of families). Mutations in CACNA1A, which encodes a neuronal calcium channel, are present in 50 percent of families with hemiplegic migraine, including all… CONTINUE READING

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