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Acta Neuropathologica|March 9, 2006
Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindredYasuhiko Baba, Bernardino Ghetti, Matthew C Baker, et al.Archives of Neurology|June 12, 2002
Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French familyYoshio Tsuboi, Ryan J Uitti, Marie-Bernadette Delisle, et al.Neurologia I Neurochirurgia Polska|October 4, 2018
TRIO gene segregation in a family with cerebellar ataxiaRana Hanna Al Shaikh, Thomas Caulfield, Audrey J Strongosky, et al.Journal of the Neurological Sciences|February 7, 2018
Comparison of clinical features among Parkinson's disease subtypes: A large retrospective study in a single centerTakuya Konno, Angela Deutschländer, Michael G Heckman, et al.Annals of Neurology|January 20, 2026
Novel Aggressive Subtype of Multiple System Atrophy Identified by Unsupervised Machine LearningHiroaki Sekiya, Daisuke Ono, Alexia R Maier, et al.Annals of Clinical and Translational Neurology|August 9, 2020
Association of MAPT subhaplotypes with clinical and demographic features in Parkinson's diseaseAngela B Deutschlander, Takuya Konno, Alexandra I Soto-Beasley, et al.Journal of Neuropathology and Experimental Neurology|May 13, 2006
Atypical progressive supranuclear palsy with corticospinal tract degenerationKeith A Josephs, Omi Katsuse, Dayne A Beccano-Kelly, et al.Parkinsonism & Related Disorders|December 2, 2008
Genetic factors influencing age at onset in LRRK2-linked Parkinson diseaseYulia Golub, Daniela Berg, Donald B Calne, et al.Parkinsonism & Related Disorders|December 3, 2015
Association of Parkinson disease age of onset with DRD2, DRD3 and GRIN2B polymorphismsAnhar Hassan, Michael G Heckman, J E Ahlskog, et al.Acta Neuropathologica|March 21, 2002
Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonismZ K Wszolek, K Gwinn-Hardy, E K Wszolek, et al.Pageof 31