Genetics of migraine headache in children

Current Pain and Headache Reports

Volumn 11, Issue 5, 2007, Pages 390-395

  Hershey, Andrew D ^a  

^a CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); DIPEPTIDYL CARBOXYPEPTIDASE; MATRIX METALLOPROTEINASE; OREXIN 2 RECEPTOR; POTASSIUM CHANNEL; SEROTONIN TRANSPORTER;

CHILD; CLINICAL OBSERVATION; ENVIRONMENTAL FACTOR; FAMILIAL HEMIPLEGIC MIGRAINE; FAMILY; FAMILY HISTORY; GENE IDENTIFICATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENOTYPE PHENOTYPE CORRELATION; HUMAN; INHERITANCE; MIGRAINE; MOLECULAR GENETICS; PATHOPHYSIOLOGY; POPULATION RESEARCH; RECURRENT DISEASE; REVIEW; TWINS;

CHILD; FAMILY; HUMANS; MIGRAINE DISORDERS; MOLECULAR BIOLOGY; POPULATION; TWIN STUDIES;

EID: 34848829118     PISSN: 15313433     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11916-007-0222-4     Document Type: Review

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