Sporadic hemiplegic migraine: Stamp collecting or food for thought?

Neurology

Volumn 60, Issue 4, 2003, Pages 536-537

  Goadsby, Peter J ^a  

^a NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL;

BRAIN STEM; DISEASE CLASSIFICATION; EDITORIAL; FAMILIAL DISEASE; HEMIPLEGIA; HUMAN; MIGRAINE; MISSENSE MUTATION; MUSCLE WEAKNESS; PHENOTYPE; PRIORITY JOURNAL; SYMPTOM;

EID: 0037465547     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000052260.98503.26     Document Type: Editorial

References (6)

1. Gowers WR. A manual of diseases of the nervous system. Philadelphia: P. Blakiston, Son & Co, 1888.
2. Russell MB, Olesen J. A nosographic analysis of the migraine aura in a general population. Brain 1996;119:355-361.
3. 2+ channel gene CACNL1A4. Cell 1996;87:543-552.
4. Thomsen LL, Ostergaard E, Olesen J, Russell MB. Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine. Neurology 2003:60:595-601.
5. Lance JW, Zagami AS. Ophthalmoplegic migraine: a recurrent demyelinating neuropathy? Cephalalgia 2001;21:84-89.
6. Ducros A, Denier C, Joutel A, et al. The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel. N Engl J Med 2001;345:17-24.