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Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1995
Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophyX H Zhong, J W Haycock, K Shannak, et al.
Acta Neuropathologica|August 13, 2008
The pathology of superficial siderosis of the central nervous systemArnulf H Koeppen, Susan C Michael, Danhong Li, et al.
Acta Neuropathologica|April 20, 2007
The dentate nucleus in Friedreich's ataxia: the role of iron-responsive proteinsArnulf H Koeppen, Susan C Michael, Mitchell D Knutson, et al.
Acta Neuropathologica|September 4, 2009
The dorsal root ganglion in Friedreich's ataxiaArnulf H Koeppen, Jennifer A Morral, Ashley N Davis, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 24, 2013
A novel transgenic rat model for spinocerebellar ataxia type 17 recapitulates neuropathological changes and supplies in vivo imaging biomarkersAlexandra Kelp, Arnulf H Koeppen, Elisabeth Petrasch-Parwez, et al.
Journal of the Neurological Sciences|June 10, 2011
Mortality in Friedreich ataxiaAmy Y Tsou, Erin K Paulsen, Sarah J Lagedrost, et al.
Cerebellum (London, England)|May 8, 2012
Friedreich's ataxia causes redistribution of iron, copper, and zinc in the dentate nucleusArnulf H Koeppen, R Liane Ramirez, Devin Yu, et al.
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