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Annals of Neurology|May 31, 2013
Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosisSorana Ciura, Serena Lattante, Isabelle Le Ber, et al.Frontiers in Neurology|January 9, 2019
A Meta-Analysis of α-Synuclein Multiplication in Familial ParkinsonismAdam Book, Ilaria Guella, Tara Candido, et al.Proceedings of the National Academy of Sciences of the United States of America|December 4, 2004
Lentiviral vector delivery of parkin prevents dopaminergic degeneration in an alpha-synuclein rat model of Parkinson's diseaseChristophe Lo Bianco, Bernard L Schneider, Matthias Bauer, et al.Orthopaedics & Traumatology, Surgery & Research : OTSR|March 17, 2025
How is familial idiopathic scoliosis transmitted? Analysis of 26 pedigreesSerge Zakine, Hugo Marty, Thomas Courtin, et al.Experimental Eye Research|July 20, 2002
Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotypeTomas S Aleman, Artur V Cideciyan, Nicholas J Volpe, et al.Neurobiology of Disease|August 25, 2010
Amyloid precursor-like protein 2 cleavage contributes to neuronal intranuclear inclusions and cytotoxicity in spinocerebellar ataxia-7 (SCA7)Junko Takahashi-Fujigasaki, Tilo Breidert, Hiroto Fujigasaki, et al.Parkinsonism & Related Disorders|August 23, 2008
A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutationsEbba Lohmann, Laurence Leclere, Francesca De Anna, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 13, 2012
Parkinson's disease patients show reduced cortical-subcortical sensorimotor connectivityMichael Sharman, Romain Valabregue, Vincent Perlbarg, et al.Journal of Neuropathology and Experimental Neurology|August 20, 2010
Leucine-rich repeat kinase 2 is associated with the endoplasmic reticulum in dopaminergic neurons and accumulates in the core of Lewy bodies in Parkinson diseaseJérémie Vitte, Sabine Traver, André Maués De Paula, et al.American Journal of Human Genetics|March 25, 2008
Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson diseaseCorinne Lautier, Stefano Goldwurm, Alexandra Dürr, et al.Pageof 50