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Molecular and Cellular Neurosciences|May 7, 2011
Cellular distribution and subcellular localization of spatacsin and spastizin, two proteins involved in hereditary spastic paraplegiaReena Prity Murmu, Elodie Martin, Agnès Rastetter, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|May 5, 2011
Fronto-temporal lobar degeneration: neuropathology in 60 casesDanielle Seilhean, Isabelle Le Ber, Marie Sarazin, et al.Nature Cell Biology|October 6, 2009
Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's diseaseCristine Alves da Costa, Claire Sunyach, Emilie Giaime, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
A new F-box protein 7 gene mutation causing typical Parkinson's diseaseEbba Lohmann, Anne-Sophie Coquel, Aurélie Honoré, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2015
In vivo neurometabolic profiling in patients with spinocerebellar ataxia types 1, 2, 3, and 7Isaac M Adanyeguh, Pierre-Gilles Henry, Tra M Nguyen, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 26, 2008
Huntington's disease-like 2 in Brazil--report of 4 patientsGuilherme G Riccioppo Rodrigues, Ruth H Walker, Alexis Brice, et al.Neurobiology of Disease|February 15, 2008
Association study of the GAB2 gene with the risk of developing Alzheimer's diseaseJulien Chapuis, Didier Hannequin, Florence Pasquier, et al.American Journal of Human Genetics|October 13, 2015
A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar AtaxiaMarie Coutelier, Iulia Blesneac, Arnaud Monteil, et al.Archives of Neurology|May 10, 2006
Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneityAlexander Lossos, Giovanni Stevanin, Vardiella Meiner, et al.Brain : a Journal of Neurology|January 23, 2004
Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patientsIsabelle Le Ber, Naïma Bouslam, Sophie Rivaud-Péchoux, et al.Pageof 50