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Cerebellum (London, England)|December 16, 2022
Patients' Perspective in Hereditary AtaxiaSorina Gorcenco, Christin Karremo, Andreas Puschmann
Cerebellum (London, England)|May 13, 2015
Case Study: Somatic Sprouts and Halo-Like Amorphous Materials of the Purkinje Cells in Huntington's DiseaseKenji Sakai, Chiho Ishida, Akiyoshi Morinaga, et al.
Cerebellum (London, England)|April 10, 2020
Neuroimaging Spectrum at Pre-, Early, and Late Symptomatic Stages of SCA17 MiceChiao-Chi Chen, Nai-Wei Yao, Chia-Wei Lin, et al.
Cerebellum (London, England)|April 18, 2020
Cerebellar Scholars' Challenging Time in COVID-19 PandemiaAasef G Shaikh, Hiroshi Mitoma, Mario Manto
Cerebellum (London, England)|December 4, 2010
Spinocerebellar ataxia type 2 (SCA2): identification of early brain degeneration in one monozygous twin in the initial disease stageFranziska Hoche, Laszlo Balikó, Wilfred den Dunnen, et al.
Cerebellum (London, England)|February 3, 2011
Sleep disorders in machado-joseph disease: frequency, discriminative thresholds, predictive values, and correlation with ataxia-related motor and non-motor featuresJosé Luiz Pedroso, Pedro Braga-Neto, André Carvalho Felício, et al.
Cerebellum (London, England)|February 16, 2011
Candidate screening of the TRPC3 gene in cerebellar ataxiaEsther B E Becker, Brent L Fogel, Sanjeev Rajakulendran, et al.
Cerebellum (London, England)|March 9, 2011
Glial S100B protein modulates mutant ataxin-1 aggregation and toxicity: TRTK12 peptide, a potential candidate for SCA1 therapyParminder J S Vig, Scoty Hearst, Qingmei Shao, et al.
Cerebellum (London, England)|April 14, 2010
Novel approaches to studying the genetic basis of cerebellar developmentSamin A Sajan, Kathryn E Waimey, Kathleen J Millen
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