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Human Mutation|October 15, 2008
Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10Cyril Goizet, Amir Boukhris, Emeline Mundwiller, et al.Neurobiology of Aging|August 3, 2014
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansionsSerena Lattante, Isabelle Le Ber, Daniela Galimberti, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2016
Clinical-genetic model predicts incident impulse control disorders in Parkinson's diseaseJulia Kraemmer, Kara Smith, Daniel Weintraub, et al.Movement Disorders Clinical Practice|January 30, 2026
Risk of Falls and Need of Walking Aid in Parkinson's Disease: Incidence and Impact of ComorbiditiesLouise-Laure Mariani, Benjamin Dano, Marion Houot, et al.Brain : a Journal of Neurology|January 26, 2006
Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3Stephan Klebe, Hamid Azzedine, Alexandra Durr, et al.Molecular Biology of the Cell|June 8, 2007
Parkin-mediated monoubiquitination of the PDZ protein PICK1 regulates the activity of acid-sensing ion channelsMonica Joch, Ariel R Ase, Carol X-Q Chen, et al.JAMA Neurology|September 29, 2015
A 22-Year Follow-up Study of Long-term Cardiac Outcome and Predictors of Survival in Friedreich AtaxiaFrancoise Pousset, Lise Legrand, Marie-Lorraine Monin, et al.Journal of Neurology|February 19, 2009
SPG11 spastic paraplegia. A new cause of juvenile parkinsonismMathieu Anheim, Clotilde Lagier-Tourenne, Giovanni Stevanin, et al.Neurogenetics|July 2, 2010
A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosumAmir Boukhris, Imed Feki, Nizar Elleuch, et al.Molecular Neurodegeneration|July 29, 2016
Lentiviral vector-mediated overexpression of mutant ataxin-7 recapitulates SCA7 pathology and promotes accumulation of the FUS/TLS and MBNL1 RNA-binding proteinsSandro Alves, Thibaut Marais, Maria-Grazia Biferi, et al.Pageof 50