Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Singh, S; Sethi, I; Francheschetti, S et al. (2006) Novel NHLRC1 mutations and genotype-phenotype correlations in patients with Lafora's progressive myoclonic epilepsy. J Med Genet 43:e48
Ganesh, Subramaniam; Delgado-Escueta, Antonio V; Suzuki, Toshimitsu et al. (2002) Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype. Hum Mol Genet 11:1263-71
Minassian, B A; Ianzano, L; Delgado-Escueta, A V et al. (2000) Identification of new and common mutations in the EPM2A gene in Lafora disease. Neurology 54:488-90
Sugimoto, Y; Morita, R; Amano, K et al. (2000) Childhood absence epilepsy in 8q24: refinement of candidate region and construction of physical map. Genomics 68:264-72
Houser, C R (1999) Neuronal loss and synaptic reorganization in temporal lobe epilepsy. Adv Neurol 79:743-61
Olsen, R W; DeLorey, T M; Gordey, M et al. (1999) GABA receptor function and epilepsy. Adv Neurol 79:499-510
Minassian, B A; Sainz, J; Serratosa, J M et al. (1999) Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy. Ann Neurol 45:262-5
Morita, R; Miyazaki, E; Shah, P U et al. (1999) Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24. Epilepsy Res 37:151-8
Lalande, M; Minassian, B A; DeLorey, T M et al. (1999) Parental imprinting and Angelman syndrome. Adv Neurol 79:421-9
Minassian, B A; DeLorey, T M; Olsen, R W et al. (1998) Angelman syndrome: correlations between epilepsy phenotypes and genotypes. Ann Neurol 43:485-93

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