Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine

Archives of Neurology

Volumn 59, Issue 6, 2002, Pages 1016-1018

  Terwindt, Gisela ^a   Kors, Esther ^a   Haan, Joost ^a,b   Vermeulen, Frans ^a   Van Den Maagdenberg, Arn ^a   Frants, Rune ^a   Ferrari, Michel ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RIJNLAND HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL;

ADOLESCENT; AGED; ARTICLE; ATAXIA; AUTOSOMAL DOMINANT DISORDER; CACNA1A GENE; CEREBELLUM ATROPHY; CHROMOSOME 19Q; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; GENE MUTATION; GENE SEQUENCE; GENE STRUCTURE; GENETIC SCREENING; HUMAN; MIGRAINE; MUTATIONAL ANALYSIS; NYSTAGMUS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; SPORADIC HEMIPLEGIC MIGRAINE;

EID: 0036279411     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.59.6.1016     Document Type: Article

References (15)

1. Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain
2. 2+ channel gene CACNL1A4
3. A new locus for hemiplegic migraine maps to chromosome 1q31
4. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
5. Sporadic hemiplegic migraine with de novo CACNA1A missense mutation
6. Genetic heterogeneity in Italian families with familial hemiplegic migraine
7. Recurrence of the T666M calcium channel CACNA1A gene mutation in familial herniplegic migraine with progressive cerebellar ataxia
8. The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
9. Alternating hemiplegia of childhood: No mutations in the familial hemiplegic migraine CACNA1A gene
10. Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene
11. Sporadic cases of possible genetic diseases: To test or not to test?
12. A new CAONA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia
13. Is familial hemiplegic migraine the hereditary form of basilar artery migraine?
14. Familial hemiplegic migraine: A clinical comparison of families linked and unlinked to chromosome 19
15. Delayed cerebral edema and fatal coma after minor head trauma: Role of the OACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine