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BMC Geriatrics
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June 15, 2018
Comprehensive pharmaceutical care to prevent drug-related readmissions of dependent-living elderly patients: a randomized controlled trial
R Lenssen, K Schmitz, C Griesel, et al.
Brain : a Journal of Neurology
|
October 23, 2003
MRI-based volumetric differentiation of sporadic cerebellar ataxia
K Burk, C Globas, T Wahl, et al.
Molecular and Cellular Neurosciences
|
April 21, 2001
Cascade of caspase activation in potassium-deprived cerebellar granule neurons: targets for treatment with peptide and protein inhibitors of apoptosis
E Gerhardt, S Kügler, M Leist, et al.
Brain Research
|
March 25, 1996
NGF, BDNF and NT-5, but not NT-3 protect against MPP+ toxicity and oxidative stress in neonatal animals
P B Kirschner, B G Jenkins, J B Schulz, et al.
Experimental Neurology
|
October 1, 1994
Systemic or local administration of azide produces striatal lesions by an energy impairment-induced excitotoxic mechanism
E Brouillet, B T Hyman, B G Jenkins, et al.
Brain Research
|
April 27, 1999
Glutathione depletion and neuronal cell death: the role of reactive oxygen intermediates and mitochondrial function
U Wüllner, J Seyfried, P Groscurth, et al.
Experimental Cell Research
|
July 2, 1999
MPP+ inhibits proliferation of PC12 cells by a p21(WAF1/Cip1)-dependent pathway and induces cell death in cells lacking p21(WAF1/Cip1)
F Soldner, M Weller, S Haid, et al.
Journal of Neurochemistry
|
August 1, 1995
3-Nitropropionic acid neurotoxicity is attenuated in copper/zinc superoxide dismutase transgenic mice
M F Beal, R J Ferrante, R Henshaw, et al.
Brain : a Journal of Neurology
|
October 8, 1998
Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3
T Klockgether, M Skalej, D Wedekind, et al.
Annals of Neurology
|
October 23, 1997
Increased 3-nitrotyrosine and oxidative damage in mice with a human copper/zinc superoxide dismutase mutation
R J Ferrante, L A Shinobu, J B Schulz, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 124) with videos related to
Sort By:
Page
of 13
BMC Geriatrics
|
June 15, 2018
Comprehensive pharmaceutical care to prevent drug-related readmissions of dependent-living elderly patients: a randomized controlled trial
R Lenssen, K Schmitz, C Griesel, et al.
Brain : a Journal of Neurology
|
October 23, 2003
MRI-based volumetric differentiation of sporadic cerebellar ataxia
K Burk, C Globas, T Wahl, et al.
Molecular and Cellular Neurosciences
|
April 21, 2001
Cascade of caspase activation in potassium-deprived cerebellar granule neurons: targets for treatment with peptide and protein inhibitors of apoptosis
E Gerhardt, S Kügler, M Leist, et al.
Brain Research
|
March 25, 1996
NGF, BDNF and NT-5, but not NT-3 protect against MPP+ toxicity and oxidative stress in neonatal animals
P B Kirschner, B G Jenkins, J B Schulz, et al.
Experimental Neurology
|
October 1, 1994
Systemic or local administration of azide produces striatal lesions by an energy impairment-induced excitotoxic mechanism
E Brouillet, B T Hyman, B G Jenkins, et al.
Brain Research
|
April 27, 1999
Glutathione depletion and neuronal cell death: the role of reactive oxygen intermediates and mitochondrial function
U Wüllner, J Seyfried, P Groscurth, et al.
Experimental Cell Research
|
July 2, 1999
MPP+ inhibits proliferation of PC12 cells by a p21(WAF1/Cip1)-dependent pathway and induces cell death in cells lacking p21(WAF1/Cip1)
F Soldner, M Weller, S Haid, et al.
Journal of Neurochemistry
|
August 1, 1995
3-Nitropropionic acid neurotoxicity is attenuated in copper/zinc superoxide dismutase transgenic mice
M F Beal, R J Ferrante, R Henshaw, et al.
Brain : a Journal of Neurology
|
October 8, 1998
Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3
T Klockgether, M Skalej, D Wedekind, et al.
Annals of Neurology
|
October 23, 1997
Increased 3-nitrotyrosine and oxidative damage in mice with a human copper/zinc superoxide dismutase mutation
R J Ferrante, L A Shinobu, J B Schulz, et al.
Page
of 13