Symptomatology in children with focal sharp waves of genetic origin

European Journal of Pediatrics

Volumn 149, Issue 3, 1989, Pages 210-215

  Doose, H ^a  

^a UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CONTROLLED STUDY; ELECTROENCEPHALOGRAPHY; FAMILIAL DISEASE; FAMILY STUDY; FEMALE; FOCAL EPILEPSY; HEREDITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MENTAL DEVELOPMENT; MONOZYGOTIC TWINS; PRIORITY JOURNAL; SEIZURE; SYMPTOMATOLOGY; TWIN CONCORDANCE; DEVELOPMENTAL DISORDER; ELECTROPHYSIOLOGY; FAMILY; GENETICS; PATHOPHYSIOLOGY; PRESCHOOL CHILD; RISK FACTOR;

CHILD; CHILD, PRESCHOOL; DEVELOPMENTAL DISABILITIES; ELECTROENCEPHALOGRAPHY; ELECTROPHYSIOLOGY; EPILEPSIES, PARTIAL; FAMILY; FEMALE; HUMAN; MALE; RISK FACTORS;

EID: 0024854411     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/BF01958285     Document Type: Article

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