Genetic predisposition to severe myoclonic epilepsy in infancy

Epilepsia

Volumn 42, Issue 2, 2001, Pages 204-209

  Benlounis, A ^a   Nabbout, R ^a   Feingold, J ^b   Parmeggiani, A ^c   Guerrini, R ^d   Kaminska, A ^a   Dulac, O ^a  

^a HÔPITAL SAINT VINCENT DE PAUL   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c UNIVERSITY OF BOLOGNA   (Italy)

^d UNIVERSITY OF PISA   (Italy)

Author keywords

Absence epilepsy; Epilepsy in infancy; Febrile convulsions; Genetics of epilepsy; Idiopathic generalized epilepsy; Severe myoclonic epilepsy in infancy

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE CLASSIFICATION; ELECTROENCEPHALOGRAM; EPILEPTOGENESIS; FAMILY HISTORY; FEBRILE CONVULSION; FEMALE; GENETIC PREDISPOSITION; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; MALE; MYOCLONUS EPILEPSY; PHENOTYPE; PRIORITY JOURNAL; QUESTIONNAIRE;

ADOLESCENT; AGE FACTORS; AGE OF ONSET; CHILD; CHILD, PRESCHOOL; EPILEPSIES, MYOCLONIC; EPILEPSY, ABSENCE; EPILEPSY, GENERALIZED; FAMILY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INCIDENCE; INFANT; MALE; QUESTIONNAIRES; RESEARCH DESIGN; SEIZURES, FEBRILE; SEVERITY OF ILLNESS INDEX;

EID: 0035089519     PISSN: 00139580     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1528-1157.2001.25299.x     Document Type: Article

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