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Generalized Non-Convulsive Epilepsy: Focus on GABA-B Receptors (Paperback): C. Marescaux, M. Vergnes, R Bernasconi Generalized Non-Convulsive Epilepsy: Focus on GABA-B Receptors (Paperback)
C. Marescaux, M. Vergnes, R Bernasconi
R1,565 Discovery Miles 15 650 Ships in 10 - 15 working days

Generalized non convulsive epilepsy (GNCE), also called absence or petit mal epilepsy, is a disease appearing during childhood. EEG, clinical, pharmacological and genetic characteristics differ from those of convulsive or focal epilepsies. No underlying structural or biochemical abnormality has been identified for generalized absence seizures and the etiology of this disorder is unknown. It is unlikely that the precise pathophysiology of GNCE can be resolved in studies that focus on humans. Therefore a number of animal models reproducing the human disease have been developed. The aim of this supplementum is to characterize such models in rodents. First, recent models are extensively described. These include the genetic model of spontaneous GNCE in Strasbourg's Wistar rats and in tottering mice as well as bilateral spike and wave discharges induced by GHB, PTZ or GABA mimetics. Second, this supplementum will also provide very recent information on putative mechanisms underlying generalized absence seizures. Third, various experimental approaches aimed at investigating the neural substrate of this particular kind of epilepsy are described with various electrophysiological, pharmacological, biochemical, metabolic, ionic and molecular data. This supplementum provides an original multidisciplinary approach to the mechanisms involved in GNCE and demonstrates that rodent models are a promising tool which complements the classical feline penicillin model.

Idiopathic Generalized Epilepsies (Paperback): A Malafosse, P. Genton, E Hirsch, C. Marescaux, D. Broglin, R Bernasconi Idiopathic Generalized Epilepsies (Paperback)
A Malafosse, P. Genton, E Hirsch, C. Marescaux, D. Broglin, …
R1,952 R1,470 Discovery Miles 14 700 Save R482 (25%) Ships in 12 - 17 working days

Idiopathic generalized epilepsies are characterized by strong genetic factors and multiple clinical phenotypes; animal models of untreated epilepsies are relevant to some of the clinical syndromes found in humans. This volume is the first to confront human clinical, animal (experimental) as well as basic and applied genetic data. Main section headings: Current approaches; Familial neonatal and infantile convulsions; Absence seizures and absence epilepsy; Juvenile myoclonic epilepsy and related syndromes; Photo sensitivity; Pathophysiology of convulsive seizures; and, Fundamental and therapeutic aspects.

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