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Handbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia type 12Elizabeth O'Hearn, Susan E Holmes, Russell L Margolis
Movement Disorders : Official Journal of the Movement Disorder Society|December 16, 2003
Phenotypic features of Huntington's disease-like 2Ruth H Walker, Joseph Jankovic, Elizabeth O'Hearn, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|July 21, 2004
Cognitive impairments in cerebellar degeneration: a comparison with Huntington's diseaseJason Brandt, Iracema Leroi, Elizabeth O'Hearn, et al.
Investigational New Drugs|October 28, 2003
The alkylating agent penclomedine induces degeneration of purkinje cells in the rat cerebellumSeamus O'Reilly, Elizabeth O'Hearn, Robert F Struck, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 16, 2004
Clinical signs and symptoms in a large hereditary spastic paraparesis pedigree with a novel spastin mutationAnthony P Nicholas, Elizabeth O'Hearn, Susan E Holmes, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|March 3, 2004
Cognitive impairment and psychiatric symptoms in 133 patients with diseases associated with cerebellar degenerationChristine M Liszewski, Elizabeth O'Hearn, Iracema Leroi, et al.
The American Journal of Psychiatry|August 3, 2002
Psychopathology in patients with degenerative cerebellar diseases: a comparison to Huntington's diseaseIracema Leroi, Elizabeth O'Hearn, Laura Marsh, et al.
Advances in Neurology|April 24, 2002
Why do Purkinje cells die so easily after global brain ischemia? Aldolase C, EAAT4, and the cerebellar contribution to posthypoxic myoclonusJohn P Welsh, Genevieve Yuen, Dimitris G Placantonakis, et al.
Annals of Neurology|October 7, 2004
Huntington's Disease-like 2 (HDL2) in North America and JapanRussell L Margolis, Susan E Holmes, Adam Rosenblatt, et al.
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