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Results: 1-8 |
Results: 8
Creatine increases survival and delays motor symptoms in a transgenic animal model of Huntington's disease
Authors: Andreassen, OA Dedeoglu, A Ferrante, RJ Jenkins, BG Ferrante, KL Thomas, M Friedlich, A Browne, SE Schilling, G Borchelt, DR Hersch, SM Ross, CA Beal, MF
Citation: Oa. Andreassen et al., Creatine increases survival and delays motor symptoms in a transgenic animal model of Huntington's disease, NEUROBIOL D, 8(3), 2001, pp. 479-491
N-epsilon-(gamma-L-glutamyl)-L-lysine (GGEL) is increased in cerebrospinalfluid of patients with Huntington's disease
Authors: Jeitner, TM Bogdanov, MB Matson, WR Daikhin, Y Yudkoff, M Folk, JE Steinman, L Browne, SE Beal, MF Blass, JP Cooper, AJL
Citation: Tm. Jeitner et al., N-epsilon-(gamma-L-glutamyl)-L-lysine (GGEL) is increased in cerebrospinalfluid of patients with Huntington's disease, J NEUROCHEM, 79(5), 2001, pp. 1109-1112
Selective antibody-induced cholinergic cell and synapse loss produce sustained hippocampal and cortical hypometabolism with correlated cognitive deficits
Authors: Browne, SE Lin, L Mattsson, A Georgievska, B Isacson, O
Citation: Se. Browne et al., Selective antibody-induced cholinergic cell and synapse loss produce sustained hippocampal and cortical hypometabolism with correlated cognitive deficits, EXP NEUROL, 170(1), 2001, pp. 36-47
Frontal lobe dysfunction in progressive supranuclear palsy: Evidence for oxidative stress and mitochondrial impairment
Authors: Albers, DS Augood, SJ Park, LCH Browne, SE Martin, DM Adamson, J Hutton, M Standaert, DG Vonsattel, JPG Gibson, GE Beal, MF
Citation: Ds. Albers et al., Frontal lobe dysfunction in progressive supranuclear palsy: Evidence for oxidative stress and mitochondrial impairment, J NEUROCHEM, 74(2), 2000, pp. 878-881
Oxidative stress in Huntington's disease
Authors: Browne, SE Ferrante, RJ Beal, MF
Citation: Se. Browne et al., Oxidative stress in Huntington's disease, BRAIN PATH, 9(1), 1999, pp. 147-163
Oxidative damage to mitochondrial DNA in Huntington's disease parietal cortex
Authors: Polidori, MC Mecocci, P Browne, SE Senin, U Beal, MF
Citation: Mc. Polidori et al., Oxidative damage to mitochondrial DNA in Huntington's disease parietal cortex, NEUROSCI L, 272(1), 1999, pp. 53-56
The cerebral metabolic consequences of nitric oxide synthase deficiency: Glucose utilization in endothelial and neuronal nitric oxide synthase null mice
Authors: Browne, SE Ayata, C Huang, PL Moskowitz, MA Beal, MF
Citation: Se. Browne et al., The cerebral metabolic consequences of nitric oxide synthase deficiency: Glucose utilization in endothelial and neuronal nitric oxide synthase null mice, J CEREBR B, 19(2), 1999, pp. 144-148
Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation
Authors: Simon, DK Pulst, SM Sutton, JP Browne, SE Beal, MF Johns, DR
Citation: Dk. Simon et al., Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation, NEUROLOGY, 53(8), 1999, pp. 1787-1793
Risultati: 1-8 |