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The International Journal of Neuroscience|December 11, 2012
Mesial temporal lobe epilepsy in a patient with spinocerebellar ataxia type 13 (SCA13)Katrin Bürk, Adam Strzelczyk, Philipp S Reif, et al.Neurology|June 24, 2017
The evolving genetic risk for sporadic ALSSummer B Gibson, Jonathan M Downie, Spyridoula Tsetsou, et al.Biorxiv : the Preprint Server for Biology|July 28, 2023
A novel naïve Bayes approach to identifying grooming behaviors in the force-plate actometric platformCollin J Anderson, Roberto Cadeddu, Daria Nesterovich Anderson, et al.Human Molecular Genetics|May 20, 2017
Gene co-expression network analysis for identifying modules and functionally enriched pathways in SCA2Lance T Pflieger, Warunee Dansithong, Sharan Paul, et al.Journal of Molecular Endocrinology|September 14, 2022
Ataxin-2 in the hypothalamus at the crossroads between metabolism and clock genesSara Carmo-Silva, Marisa Ferreira-Marques, Clévio Nóbrega, et al.Neurology|May 13, 2016
Population-based risks for cancer in patients with ALSSummer B Gibson, Diana Abbott, James M Farnham, et al.Plos Genetics|January 2, 2008
dAtaxin-2 mediates expanded Ataxin-1-induced neurodegeneration in a Drosophila model of SCA1Ismael Al-Ramahi, Alma M Pérez, Janghoo Lim, et al.Neurology. Clinical Practice|August 12, 2014
State neurologic societies and the AAN: Strengthening neurology for the futurePushpa Narayanaswami, Dave Showers, Bruce Levi, et al.Plos One|April 12, 2011
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.Scientific Reports|July 29, 2015
Nuclear retention of full-length HTT RNA is mediated by splicing factors MBNL1 and U2AF65Xin Sun, Pan P Li, Shanshan Zhu, et al.Pageof 15