Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Movement Disorders and SLC2A1[original query] |
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Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder. Brain : a journal of neurology 2010 Mar 133 (Pt 3): 655-70. Leen Wilhelmina G, Klepper Joerg, Verbeek Marcel M, Leferink Maike, Hofste Tom, van Engelen Baziel G, Wevers Ron A, Arthur Todd, Bahi-Buisson Nadia, Ballhausen Diana, Bekhof Jolita, van Bogaert Patrick, Carrilho Inês, Chabrol Brigitte, Champion Michael P, Coldwell James, Clayton Peter, Donner Elizabeth, Evangeliou Athanasios, Ebinger Friedrich, Farrell Kevin, Forsyth Rob J, de Goede Christian G E L, Gross Stephanie, Grunewald Stephanie, Holthausen Hans, Jayawant Sandeep, Lachlan Katherine, Laugel Vincent, Leppig Kathy, Lim Ming J, Mancini Grazia, Marina Adela Della, Martorell Loreto, McMenamin Joe, Meuwissen Marije E C, Mundy Helen, Nilsson Nils O, Panzer Axel, Poll-The Bwee T, Rauscher Christian, Rouselle Christophe M R, Sandvig Inger, Scheffner Thomas, Sheridan Eamonn, Simpson Neil, Sykora Parol, Tomlinson Richard, Trounce John, Webb David, Weschke Bernhard, Scheffer Hans, Willemsen Michél |
Development of a rapid functional assay that predicts GLUT1 disease severity. Neurology. Genetics 2018 12 4 (6): e297. Zaman Sasha M, Mullen Saul A, Petrovski Slavé, Maljevic Snezana, Gazina Elena V, Phillips A Marie, Jones Gabriel Davis, Hildebrand Michael S, Damiano John, Auvin Stéphane, Lerche Holger, Weber Yvonne G, Berkovic Samuel F, Scheffer Ingrid E, Reid Christopher A, Petrou Stev |
Genetic analysis of dystonia-related genes in Parkinson's disease. Frontiers in aging neuroscience 2023 6 15 1207114. Yige Wang, Yuwen Zhao, Hongxu Pan, Qian Zeng, Xiaoxia Zhou, Yaqin Xiang, Zhou Zhou, Qian Xu, Qiying Sun, Jieqiong Tan, Xinxiang Yan, Jinchen Li, Jifeng Guo, Beisha Tang, Qiao Yu, Zhenhua L |
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