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Brain : a Journal of Neurology|June 30, 2010
Does corticobasal degeneration exist? A clinicopathological re-evaluationHelen Ling, Sean S O'Sullivan, Janice L Holton, et al.
Orphanet Journal of Rare Diseases|May 2, 2015
Rhabdomyolysis: a genetic perspectiveRenata Siciliani Scalco, Alice R Gardiner, Robert Ds Pitceathly, et al.
Arquivos De Neuro-Psiquiatria|July 24, 2014
From exercise intolerance to functional improvement: the second wind phenomenon in the identification of McArdle diseaseRenata Siciliani Scalco, Sherryl Chatfield, Richard Godfrey, et al.
Acta Neuropathologica Communications|November 19, 2014
Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusionsReema Paudel, Aoife Kiely, Abi Li, et al.
NPJ Parkinson'S Disease|December 7, 2023
Development and validation of an expanded antibody toolset that captures alpha-synuclein pathological diversity in Lewy body diseasesMelek Firat Altay, Senthil T Kumar, Johannes Burtscher, et al.
Muscle & Nerve|June 24, 2011
Sodium and chloride channelopathies with myositis: coincidence or connection?Emma Matthews, James A L Miller, Malcolm R MacLeod, et al.
Neuroscience Letters|April 10, 2009
Regional differences in the severity of Lewy body pathology across the olfactory cortexLaura Silveira-Moriyama, Janice L Holton, Ann Kingsbury, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 2013
Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1Sarah Finlayson, Jacqueline Palace, Katsiaryna Belaya, et al.
Brain : a Journal of Neurology|March 25, 2005
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonismDavid R Williams, Rohan de Silva, Dominic C Paviour, et al.
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