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P G Ince

Showing results (51-60 of 136) with videos related to

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Annals of Neurology|November 30, 1999
Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell deathG M Borthwick, M A Johnson, P G Ince, et al.
Neuroreport|April 15, 1999
Low expression of GluR2 AMPA receptor subunit protein by human motor neuronsP J Shaw, T L Williams, J Y Slade, et al.
Experimental Neurology|September 28, 2001
Glial cells of the spinal cord and subcortical white matter up-regulate neuronal nitric oxide synthase in sporadic amyotrophic lateral sclerosisJ M Anneser, M R Cookson, P G Ince, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1997
Fulminant encephalopathy due to the catastrophic primary antiphospholipid syndromeP F Chinnery, P J Shaw, P G Ince, et al.
Alzheimer Disease and Associated Disorders|January 1, 1995
Abnormally phosphorylated tau protein in senile dementia of Lewy body type and Alzheimer disease: evidence that the disorders are distinctC Strong, B H Anderton, R H Perry, et al.
Dementia (Basel, Switzerland)|May 1, 1995
Neuropathological diagnoses in elderly patients in Oslo: Alzheimer's disease, Lewy body disease, vascular lesionsP G Ince, F K McArthur, E Bjertness, et al.
Clinical Neuropathology|March 1, 1995
Malignant cerebrovascular thromboembolization by phaechromocytomaR Raghavan, P G Ince, T J Walls, et al.
Neurology|August 1, 1992
Adult-onset motor neuron disease and infantile Werdnig-Hoffmann disease (spinal muscular atrophy type 1) in the same familyP J Shaw, P G Ince, J Goodship, et al.
Neuroscience|January 11, 2002
The expression of the glutamate re-uptake transporter excitatory amino acid transporter 1 (EAAT1) in the normal human CNS and in motor neurone disease: an immunohistochemical studyS J Banner, A E Fray, P G Ince, et al.
Neuroreport|February 14, 1998
CNS tissue Cu/Zn superoxide dismutase (SOD1) mutations in motor neurone disease (MND)P J Shaw, J Tomkins, J Y Slade, et al.
Pageof 14

Showing results (51-60 of 136) with videos related to

Sort By:
Pageof 14
Annals of Neurology|November 30, 1999
Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell deathG M Borthwick, M A Johnson, P G Ince, et al.
Neuroreport|April 15, 1999
Low expression of GluR2 AMPA receptor subunit protein by human motor neuronsP J Shaw, T L Williams, J Y Slade, et al.
Experimental Neurology|September 28, 2001
Glial cells of the spinal cord and subcortical white matter up-regulate neuronal nitric oxide synthase in sporadic amyotrophic lateral sclerosisJ M Anneser, M R Cookson, P G Ince, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1997
Fulminant encephalopathy due to the catastrophic primary antiphospholipid syndromeP F Chinnery, P J Shaw, P G Ince, et al.
Alzheimer Disease and Associated Disorders|January 1, 1995
Abnormally phosphorylated tau protein in senile dementia of Lewy body type and Alzheimer disease: evidence that the disorders are distinctC Strong, B H Anderton, R H Perry, et al.
Dementia (Basel, Switzerland)|May 1, 1995
Neuropathological diagnoses in elderly patients in Oslo: Alzheimer's disease, Lewy body disease, vascular lesionsP G Ince, F K McArthur, E Bjertness, et al.
Clinical Neuropathology|March 1, 1995
Malignant cerebrovascular thromboembolization by phaechromocytomaR Raghavan, P G Ince, T J Walls, et al.
Neurology|August 1, 1992
Adult-onset motor neuron disease and infantile Werdnig-Hoffmann disease (spinal muscular atrophy type 1) in the same familyP J Shaw, P G Ince, J Goodship, et al.
Neuroscience|January 11, 2002
The expression of the glutamate re-uptake transporter excitatory amino acid transporter 1 (EAAT1) in the normal human CNS and in motor neurone disease: an immunohistochemical studyS J Banner, A E Fray, P G Ince, et al.
Neuroreport|February 14, 1998
CNS tissue Cu/Zn superoxide dismutase (SOD1) mutations in motor neurone disease (MND)P J Shaw, J Tomkins, J Y Slade, et al.
Pageof 14