Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes

Cephalalgia

Volumn 28, Issue 10, 2008, Pages 1039-1047

  Cuenca Leon E ^a   Corominas, R ^a   Fernandez Castillo N ^b,c   Volpini, V ^d   Del Toro, M ^a   Roig, M ^a   MacAya, A ^a   Cormand, B ^b,c  

^a HOSPITAL UNIVERSITARI VALL D HEBRON   (Spain)

^b UNIVERSITY OF BARCELONA   (Spain)

^c CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

^d BELLVITGE BIOMEDICAL RESEARCH INSTITUTE IDIBELL   (Spain)

Author keywords

Basilar type migraine; CACNA1A gene; Childhood periodic syndromes; Hemiplegic migraine; Mutation analysis

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; ATP1A2 GENE; BASILAR TYPE MIGRAINE; CACNA1A GENE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; HEMIPLEGIC MIGRAINE; HUMAN; MALE; NUCLEOTIDE SEQUENCE; PHENOTYPE; SCN1A GENE; TORTICOLLIS;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; CALCIUM CHANNELS; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; MALE; MIDDLE AGED; MIGRAINE WITH AURA; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; NERVE TISSUE PROTEINS; PEDIGREE; PERIODICITY; SODIUM CHANNELS; SODIUM-POTASSIUM-EXCHANGING ATPASE; SPAIN; TORTICOLLIS; VERTIGO;

EID: 51649112972     PISSN: 03331024     EISSN: 14682982     Source Type: Journal    
DOI: 10.1111/j.1468-2982.2008.01645.x     Document Type: Article

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