Familial temporal lobe epilepsy with febrile seizures

Neurology

Volumn 58, Issue 9, 2002, Pages 1429-1433

  Depondt, Chantal ^a   Van Paesschen, W ^a   Matthijs, G ^a   Legius, E ^a   Martens, K ^a   Demaerel, P ^a   Wilms, G ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; ELECTROENCEPHALOGRAM; FAMILIAL DISEASE; FEBRILE CONVULSION; FEMALE; FOCAL EPILEPSY; GENE LOCUS; GENETIC LINKAGE; HIPPOCAMPUS; HUMAN; INFANT; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PRIORITY JOURNAL; TEMPORAL LOBE EPILEPSY;

EID: 0037076487     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.58.9.1429     Document Type: Article

References (9)

1. Epilepsies with single gene inheritance
2. Localization of a gene for partial epilepsy to chromosome 10q
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4. Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31
5. Validation of a questionnaire for clinical seizure diagnosis
6. Proposal for revised clinical and electroencephalographic classification of epileptic seizures
7. Proposal for revised classification of epilepsies and epileptic syndromes
8. Hippocampal malrotation with normal corpus callosum: A new entity?
9. +-channel beta1 subunit gene SCN1B