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

New England Journal of Medicine

Volumn 345, Issue 1, 2001, Pages 17-24

  Ducros, Anne ^a,b   Denier, Christian ^a   Joutel, Anne ^a,b   Cecillon, Michaëlle ^a,b   Lescoat, Christelle ^a   Vahedi, Katayoun ^b   Darcel, Françoise ^c   Vicaut, Eric ^d   Bousser, Marie Germaine ^b   Tournier Lasserve, Elisabeth ^a,b  

^a INSERM   (France)

^b HÔPITAL LARIBOISIÈRE   (France)

^c RENNES UNIVERSITY HOSPITAL   (France)

^d HÔPITAL FERNAND WIDAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; CALCIUM ION;

ADOLESCENT; ADULT; AGED; ARTICLE; ATAXIA; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL FEATURE; COMA; CONTROLLED STUDY; FAMILIAL DISEASE; GENE MUTATION; GENETIC ASSOCIATION; HEMIPARESIS; HEMIPLEGIA; HUMAN; MAJOR CLINICAL STUDY; MIGRAINE; MISSENSE MUTATION; NEUROLOGIC DISEASE; NYSTAGMUS; PRIORITY JOURNAL;

AGE OF ONSET; ATAXIA; CALCIUM CHANNELS; FEMALE; GENOTYPE; HUMANS; MALE; MIGRAINE WITH AURA; MUTATION, MISSENSE; NYSTAGMUS, PATHOLOGIC; PARESIS; PEDIGREE; PHENOTYPE;

EID: 0035811775     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM200107053450103     Document Type: Article

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