Loss of cortical GABA terminals in Unverricht–Lundborg disease

Loss of cortical GABA terminals in Unverricht–Lundborg disease

Unverricht–Lundborg disease (ULD) is the most common progressive myoclonic epilepsy. Its etiology has been identified in a defect of a protease inhibitor, cystatin B (CSTB), but the mechanism(s) by which this defect translates in the clinical manifestations of the disease are still obscure. We teste...

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Manylion Llyfryddiaeth
Prif Awduron: Andrea Buzzi, Maia Chikhladze, Chiara Falcicchia, Beatrice Paradiso, Giovanni Lanza, Marie Soukupova, Matteo Marti, Michele Morari, Silvana Franceschetti, Michele Simonato
Fformat: Erthygl
Iaith:English
Cyhoeddwyd: Elsevier 2012-08-01
Cyfres:Neurobiology of Disease
Pynciau:
Epilepsy
Myoclonus
GABA
Neurodegeneration
Cortex
Mynediad Ar-lein:http://www.sciencedirect.com/science/article/pii/S0969996112001349

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http://www.sciencedirect.com/science/article/pii/S0969996112001349

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