Alternating hemiplegia of childhood: No mutations in the familial hemiplegic migraine CACNA1A gene

Cephalalgia

Volumn 20, Issue 8, 2000, Pages 696-700

  Haan, J ^a,b   Kors, Ee ^a   Terwindt, Gm ^a   Vermeulen, Flmg ^a   Vergouwe, Mn ^a   Van Den Maagdenberg, Amjm ^a   Gill, Ds ^c   Pascual, J ^d   Ophoff, Ra ^a   Frants, Rr ^a   Ferrari, Md ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RIJNLAND HOSPITAL   (Netherlands)

^c GUY S HOSPITAL   (United Kingdom)

^d HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

Author keywords

Alternating hemiplegia of childhood; CACNA1A; Familial hemiplegic migraine

Indexed keywords

ION CHANNEL;

ARTICLE; CHILD; CHROMOSOME 19; CLINICAL ARTICLE; DISEASE ASSOCIATION; DNA POLYMORPHISM; FAMILIAL DISEASE; GENE MUTATION; HEMIPLEGIA; HUMAN; MENTAL DEFICIENCY; MIGRAINE; NERVE CELL LESION; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADULT; AMINO ACID SEQUENCE; BASE SEQUENCE; CALCIUM CHANNELS; CHILD; CHILD, PRESCHOOL; FEMALE; HEMIPLEGIA; HUMANS; MALE; MIGRAINE DISORDERS; MUTATION; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0034491681     PISSN: 03331024     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.0333-1024.2000.00095.x     Document Type: Article

References (23)

1. Alternating hemiplegia of childhood
2. Alternating hemiplegia of childhood: Clinical findings and diagnostic criteria
3. Alternating hemiplegia in childhood: A report of eight patients with complicated migraine beginning in infancy
4. A syndrome of autosomal dominant alternating hemiplegia: Clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations
5. Benign familial nocturnal alternating hemiplegia of childhood
6. Autosomal dominant alternating hemiplegia of childhood
7. Genetics of primary headaches
8. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
9. A new locus for hemiplegic migraine maps to chromosome 1q31
10. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
11. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel
12. A case of alternating hemiplegia of childhood with cerebellar atrophy
13. Alternating hemiplegia of childhood: Report of a case having a long history
14. A simple salting out procedure for extracting DNA from human nucleated cells
15. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
16. Migraine, ataxia and epilepsy: A challenging spectrum of genetically determined calcium channelopathies
17. Alternating hemiplegia of childhood: Insights into its pathophysiology
18. Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene
19. Chromosomal localization of the human genes for alpha 1A, alpha 1B, and alpha 1E voltage-dependent Ca2+ channel subunits
20. Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine
21. Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM
22. Genetic heterogeneity in Italian families with familial hemiplegic migraine
23. High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2