1. R. Nabbout, I. Desguerre, S. Sabbagh, C. Depienne, P. Plouin, O. Dulac, and C. Chiron. An unexpected EEG course in Dravet syndrome. Epilepsy Res, 81(1):90-5, 2008. Note: Journal ArticleNetherlands. [WWW] Keyword(s): Adolescent, Age of Onset, Anticonvulsants/therapeutic use, Child, Cognition/physiology, Developmental Disabilities/complications, *Electroencephalography, Electromyography, Epilepsy, Tonic-Clonic/diagnosis/genetics/*physiopathology, Female, Fever/complications, Humans, Male, Mutation, Myoclonic Epilepsy, Juvenile/diagnosis/genetics/*physiopathology, Nerve Tissue Proteins/genetics, Sodium Channels/genetics, Syndrome.



2. R. Nabbout, S. Baulac, I. Desguerre, N. Bahi-Buisson, C. Chiron, M. Ruberg, O. Dulac, and E. LeGuern. New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p. Neurology, 68(17):1374-81, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Child, Preschool, Chromosomes, Human, Pair 18/*genetics, Chromosomes, Human, Pair 3/*genetics, Electroencephalography, Epilepsy, Absence/*genetics, Epilepsy, Temporal Lobe/genetics, Epilepsy, Tonic-Clonic/genetics, *Epistasis, Genetic, Female, France, Genes, Genetic Markers, Genotype, Haplotypes, Hippocampus/pathology, Humans, Infant, Magnetic Resonance Imaging, Male, Pedigree, Penetrance, Phenotype, Sclerosis/pathology, Seizures, Febrile/*genetics.



3. R. Nabbout, S. Baulac, N. Bahi-Buisson, C. Chiron, O. Dulac, and E. Leguern. A French family with febrile seizures and childhood absence epilepsy. Epilepsia, 47:369-370, 2006. Note: Suppl. 4. [WWW]



4. R. Nabbout, A. Kozlovski, E. Gennaro, N. Bahi-Buisson, F. Zara, C. Chiron, A. Bianchi, A. Brice, E. Leguern, and O. Dulac. Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy. Epilepsy Res, 56(2-3):127-33, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tNetherlands. [WWW] Keyword(s): Child, Preschool, DNA/genetics, Epilepsies, Myoclonic/*genetics, Epilepsy, Generalized/*genetics, Female, Humans, Male, Mutation, Nerve Tissue Proteins/genetics, Polymorphism, Single Nucleotide/genetics, Seizures, Febrile/*genetics, Sodium Channels/genetics, ras Guanine Nucleotide Exchange Factors/*genetics.

This material is presented to ensure timely dissemination of scholarly and technical work. Copyright and all rights therein are retained by authors or by other copyright holders. All person copying this information are expected to adhere to the terms and constraints invoked by each author's copyright. In most cases, these works may not be reposted without the explicit permission of the copyright holder.

Les documents contenus dans ces répertoires sont rendus disponibles par les auteurs qui y ont contribué en vue d'assurer la diffusion à temps de travaux savants et techniques sur une base non-commerciale. Les droits de copie et autres droits sont gardés par les auteurs et par les détenteurs du copyright, en dépit du fait qu'ils présentent ici leurs travaux sous forme électronique. Les personnes copiant ces informations doivent adhérer aux termes et contraintes couverts par le copyright de chaque auteur. Ces travaux ne peuvent pas être rendus disponibles ailleurs sans la permission explicite du détenteur du copyright.

This document was translated from BibT_EX by bibtex2html