Defining the phenotype to discover the genotype

Neurology

Volumn 66, Issue 11, 2006, Pages 1622-1623

  Gurnett, Christina A ^a   Trevathan, Edwin ^a,b  

^a ST LOUIS CHILDREN S HOSPITAL   (United States)

^b WASHINGTON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATAXIC APHASIA; CLASSIFICATION; DIAGNOSTIC VALUE; EDITORIAL; EPILEPSY; FOCAL EPILEPSY; GENOTYPE; HUMAN; HUMAN GENOME PROJECT; NOMENCLATURE; PHENOTYPE; PRIORITY JOURNAL; RETROSPECTIVE STUDY;

BIOLOGICAL MARKERS; BRAIN; EPILEPSY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; NERVE TISSUE PROTEINS; PHENOTYPE; RISK ASSESSMENT; RISK FACTORS;

EID: 33745669944     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000224695.39903.b9     Document Type: Editorial

References (7)

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2. Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy. Epilepsia 1989;30:389-399.
3. Choi H, Winawer MR, Kalachikov S, Pedley TA, Hauser WA, Ottman R. Classification of partial seizure symptoms in genetic studies of the epilepsies. Neurology 2006;66:1648-1653.
4. Blume WT, Luders HO, Mizrahi E, Tassinari C, van Emde Boas W, Engel J Jr.. Glossary of descriptive terminology for ictal semiology: report of the ILAE task force on classification and terminology. Epilepsia 2001;42:1212-1218.
5. Luders HO, Acharya J, Baumgartner C, et al. Semiological seizure classification. Epilepsia 1998;39:1006-1013.
6. Berkovic SF, Izzillo P, McMahon JM, et al. LGI1 mutations in temporal lobe epilepsies. Neurology 2004;62:1115-1119.
7. Ottman R, Winawer MR, Kalchikov S, et al. LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology 2004;62:1120-1126.