首页 | 本学科首页   官方微博 | 高级检索  
     


Alterations in the α2δ ligand,thrombospondin‐1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies
Authors:Milena Cannella  Tiziana Imbriglio  Michela Guiducci  Pasquale Parisi  Julian Schubert  Michele Iacomino  Federico Zara  Holger Lerche  Slavianka Moyanova  Richard Teke Ngomba  Gilles van Luijtelaar  Giuseppe Battaglia  Valeria Bruno  Pasquale Striano  Ferdinando Nicoletti
Affiliation:1. I.R.C.C.S. Neuromed, Pozzilli, Italy;2. Departments of Neurosciences, Mental Health and Sensory Organs, University Sapienza, Rome, Italy;3. Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany;4. Laboratory of Neurogenetics, “G. Gaslini” Institute, Genova, Italy;5. School of Pharmacy, University of Lincoln, Lincoln, United Kingdom;6. Donders Center for Cognition, Radboud University, Nijmegen, The Netherlands;7. Departments of Physiology and Pharmacology, University Sapienza, Rome, Italy;8. Pediatric Neurology and Muscular Diseases Unit, Departments of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, “G. Gaslini” Institute, University of Genoa, Genova, Italy
Abstract:
Keywords:Thrombospondins  Absence epilepsy  α     subunit  WAG/Rij rats  Genetic variants
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号