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Volumn 29, Issue 4, 1999, Pages 375-380
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Opercular epileptic syndrome: An unusual form of benign partial epilepsy in childhood;El sindrome opercular epileptico: Una forma peculiar de epilepsia parcial benigna de la infancia con paroxismos rolandicos
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Author keywords
Benign epilepsy with centrotemporal rolandic spikes; Benign neonatal familial convulsions; Continuous spike and wave during slow sleep. Opercular syndrome; Worsening of seizures by antiepileptic drugs
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Indexed keywords
ANTICONVULSIVE AGENT;
CARBAMAZEPINE;
CLOBAZAM;
PHENOBARBITAL;
PHENYTOIN;
ARTICLE;
BENIGN CHILDHOOD EPILEPSY;
CASE REPORT;
CHILD;
CLINICAL FEATURE;
DISEASE EXACERBATION;
DYSPRAXIA;
ELECTROENCEPHALOGRAM;
HUMAN;
HUMAN CELL;
HUMAN TISSUE;
LANGUAGE DISABILITY;
MALE;
OPERCULAR EPILEPTIC SYNDROME;
SYNDROME DELINEATION;
ADOLESCENT;
ADULT;
APRAXIA;
CHEMICALLY INDUCED DISORDER;
COGNITIVE DEFECT;
ELECTROENCEPHALOGRAPHY;
FEMALE;
GENETICS;
HOSPITALIZATION;
NEUROPSYCHOLOGICAL TEST;
ROLANDIC EPILEPSY;
ADOLESCENT;
ADULT;
ANTICONVULSANTS;
APRAXIAS;
COGNITION DISORDERS;
ELECTROENCEPHALOGRAPHY;
EPILEPSY, ROLANDIC;
FEMALE;
HUMANS;
MALE;
NEUROPSYCHOLOGICAL TESTS;
SEVERITY OF ILLNESS INDEX;
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EID: 0033575550
PISSN: 02100010
EISSN: None
Source Type: Journal
DOI: 10.33588/rn.2904.99028 Document Type: Article |
Times cited : (16)
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References (20)
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