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Brain : a Journal of Neurology|October 1, 1996
Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3K Bürk, M Abele, M Fetter, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 7, 1998
Potassium deprivation-induced apoptosis of cerebellar granule neurons: cytochrome c release in the absence of altered expression of Bcl-2 family proteinsM Gleichmann, S Beinroth, J C Reed, et al.
Brain : a Journal of Neurology|April 29, 1999
Cognitive deficits in spinocerebellar ataxia 2K Bürk, C Globas, S Bösch, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 21, 2004
Dopamine transporter SPECT in patients with mitochondrial disordersM Minnerop, C Kornblum, A Y Joe, et al.
Biochemical and Biophysical Research Communications|February 13, 2001
Overexpression of bcl-2 results in reduction of cytochrome c content and inhibition of complex I activityC S Schwarz, B O Evert, J Seyfried, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1989
The basal ganglia, the deep prepyriform cortex, and seizure spread: bicuculline is anticonvulsant in the rat striatumL Turski, E A Cavalheiro, L S Calderazzo-Filho, et al.
Annals of Neurology|November 18, 1998
The phenotypic spectrum of CADASIL: clinical findings in 102 casesM Dichgans, M Mayer, I Uttner, et al.
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