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Neurobiology of Disease|January 31, 2006
Gene expression profiling in frataxin deficient mice: microarray evidence for significant expression changes without detectable neurodegenerationGiovanni Coppola, Sang-Hyun Choi, Manuela M Santos, et al.Human Molecular Genetics|April 21, 2009
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARgamma pathway as a therapeutic target in Friedreich's ataxiaGiovanni Coppola, Daniele Marmolino, Daning Lu, et al.Nature Reviews. Neurology|April 7, 2009
Diagnosis and treatment of Friedreich ataxia: a European perspectiveJörg B Schulz, Sylvia Boesch, Katrin Bürk, et al.Current Aging Science|May 13, 2017
The Click Test: A Novel Tool to Quantify the Age-Related Decline of Fast Motor Sequencing of the ThumbFlorian Bodranghien, Helene Mahe, Benjamin Baude, et al.Cerebellum (London, England)|August 11, 2021
Consensus Paper: Strengths and Weaknesses of Animal Models of Spinocerebellar Ataxias and Their Clinical ImplicationsJan Cendelin, Marija Cvetanovic, Mandi Gandelman, et al.Journal of Child Neurology|August 15, 2002
Friedreich's ataxia associated with mitochondrial myopathy: clinicopathologic reportCatherine L Gallagher, Andrew J Waclawik, Brad R Beinlich, et al.DNA and Cell Biology|August 9, 2007
Gene set enrichment analyses revealed several affected pathways in Niemann-pick disease type C fibroblastsAloys De Windt, Myriam Rai, Leena Kytömäki, et al.Neurology|February 27, 2015
Quantifiable evaluation of cerebellar signs in childrenAntoine Filipovic Pierucci, Caterina Mariotti, Marta Panzeri, et al.Cerebellum (London, England)|July 26, 2003
Iron metabolism in mice with partial frataxin deficiencyManuela M Santos, Carlos J Miranda, Joanne E Levy, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 23, 2009
Grafting neural precursor cells promotes functional recovery in an SCA1 mouse modelSatyan Chintawar, Raphael Hourez, Ajay Ravella, et al.Pageof 35