Adult myoclonic epilepsy: A distinct syndrome of idiopathic generalized epilepsy

Neurology

Volumn 55, Issue 7, 2000, Pages 1030-1033

  Gilliam, Frank ^a   Steinhoff, B J ^b   Bittermann, H J ^b   Kuzniecky, R ^c   Faught, E ^c   Abou Khalil, B ^d  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF GÖTTINGEN   (Germany)

^c UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^d VANDERBILT UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABSENCE; ADULT; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; ELECTROENCEPHALOGRAPHY; EPILEPTIC DISCHARGE; FAMILY HISTORY; GENERALIZED EPILEPSY; HUMAN; IDIOPATHIC DISEASE; MYOCLONUS EPILEPSY; ONSET AGE; PRIORITY JOURNAL; SYNDROME; TONIC CLONIC SEIZURE;

EID: 0034633671     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.55.7.1030     Document Type: Article

References (10)

1. A revised proposal for the classification of epilepsy and epileptic syndromes
2. The idiopathic generalized epilepsies of adolescence with childhood and juvenile age of onset
3. 'Aufwach'-epilepsien
4. Epilepsy in twins
5. Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6
6. Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy
7. Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
8. Juvenile myoclonic epilepsy in unexpected age groups
9. Quantitative MRI in patients with idiopathic generalized epilepsy. Evidence of widespread cerebral structural changes
10. Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24