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Neuroscience Letters|March 14, 1994
Unaltered aconitase activity, but decreased complex I activity in substantia nigra pars compacta of patients with Parkinson's diseaseB Janetzky, S Hauck, M B Youdim, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1989
An antigenic profile of Lewy bodies: immunocytochemical indication for protein phosphorylation and ubiquitinationC Bancher, H Lassmann, H Budka, et al.
Neuroscience Letters|May 2, 2002
Unaltered brain levels of 1,N2-propanodeoxyguanosine adducts of trans-4-hydroxy-2-nonenal in Alzheimer's diseaseM E Götz, M Wacker, C Luckhaus, et al.
Journal of Neural Transmission. Supplementum|January 1, 1993
How to run a brain bank. A report from the Austro-German brain bankW Gsell, K W Lange, R Pfeuffer, et al.
Neuroscience Letters|June 16, 2000
Human post-mortem striatal alpha4beta2 nicotinic acetylcholine receptor density in schizophrenia and Parkinson's syndromeN Durany, R Zöchling, K W Boissl, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1996
Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological studyI Litvan, C A Mangone, A McKee, et al.
Brain : a Journal of Neurology|January 1, 1997
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological studyI Litvan, G Campbell, C A Mangone, et al.
Journal of Neural Transmission. Supplementum|January 1, 1995
Effect of lazaroid U-74389G on iron-induced reduction of striatal dopamine metabolismW Wesemann, M Solbach, R Nafe, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 21, 2011
Neuromyelitis optica spectrum disorders in patients with myasthenia gravis: ten new aquaporin-4 antibody positive cases and a review of the literatureS Jarius, F Paul, D Franciotta, et al.
Neurology|November 1, 1994
Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)J J Hauw, S E Daniel, D Dickson, et al.
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