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S E Daniel

Showing results (71-80 of 93) with videos related to

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Neurology|December 31, 1997
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degenerationO Bandmann, M G Sweeney, S E Daniel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 21, 1999
The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseasesH R Morris, J C Janssen, O Bandmann, et al.
Journal of Neurochemistry|September 1, 1997
Oxidative DNA damage in the parkinsonian brain: an apparent selective increase in 8-hydroxyguanine levels in substantia nigraZ I Alam, A Jenner, S E Daniel, et al.
Neuroscience|May 1, 1995
Preproenkephalin and preprotachykinin messenger RNA expression in normal human basal ganglia and in Parkinson's diseaseA P Nisbet, O J Foster, A Kingsbury, et al.
Neuroscience|November 1, 1996
Glutamate decarboxylase-67 messenger RNA expression in normal human basal ganglia and in Parkinson's diseaseA P Nisbet, D J Eve, A E Kingsbury, 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.
Journal of Neurochemistry|December 1, 1990
Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's diseaseA H Schapira, V M Mann, J M Cooper, et al.
Lancet (London, England)|September 24, 1994
Incidental Lewy body disease in black AfricansK Jendroska, B J Olasode, S E Daniel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1997
Mitochondrial respiratory chain function in multiple system atrophyM Gu, M T Gash, J M Cooper, et al.
Annals of Neurology|October 1, 1992
Alpha-tocopherol levels in brain are not altered in Parkinson's diseaseD T Dexter, R J Ward, F R Wells, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
Neurology|December 31, 1997
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degenerationO Bandmann, M G Sweeney, S E Daniel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 21, 1999
The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseasesH R Morris, J C Janssen, O Bandmann, et al.
Journal of Neurochemistry|September 1, 1997
Oxidative DNA damage in the parkinsonian brain: an apparent selective increase in 8-hydroxyguanine levels in substantia nigraZ I Alam, A Jenner, S E Daniel, et al.
Neuroscience|May 1, 1995
Preproenkephalin and preprotachykinin messenger RNA expression in normal human basal ganglia and in Parkinson's diseaseA P Nisbet, O J Foster, A Kingsbury, et al.
Neuroscience|November 1, 1996
Glutamate decarboxylase-67 messenger RNA expression in normal human basal ganglia and in Parkinson's diseaseA P Nisbet, D J Eve, A E Kingsbury, 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.
Journal of Neurochemistry|December 1, 1990
Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's diseaseA H Schapira, V M Mann, J M Cooper, et al.
Lancet (London, England)|September 24, 1994
Incidental Lewy body disease in black AfricansK Jendroska, B J Olasode, S E Daniel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1997
Mitochondrial respiratory chain function in multiple system atrophyM Gu, M T Gash, J M Cooper, et al.
Annals of Neurology|October 1, 1992
Alpha-tocopherol levels in brain are not altered in Parkinson's diseaseD T Dexter, R J Ward, F R Wells, et al.
Pageof 10