Abstract
Animal models of human brain disorders permit to explore disease mechanisms and to test potential therapies. However therapeutic molecules derived from animal models often translate poorly to the clinic. While human data may be more relevant, experiments on patients are constrained and living tissue is unavailable for many disorders. Here we compare work on animal models and on human tissue for three epileptic syndromes where human tissue is excised therapeutically. (1) acquired temporal lobe epilepsies, (2) inherited epilepsies associated with ...
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