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P G Ince

Showing results (31-40 of 136) with videos related to

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Acta Neuropathologica|October 1, 1996
Familial amyotrophic lateral sclerosis with a mutation in exon 4 of the Cu/Zn superoxide dismutase gene: pathological and immunocytochemical changesP G Ince, P J Shaw, J Y Slade, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1991
Lower motor neuron degeneration and familial predisposition to colonic neoplasia in two adult siblingsP J Shaw, P G Ince, J Slade, et al.
Brain Research|January 18, 1991
The quantitative autoradiographic distribution of [3H]MK-801 binding sites in the normal human spinal cordP J Shaw, P G Ince, M Johnson, et al.
Acta Neuropathologica|January 1, 1995
Parkinsonism in motor neuron disease: case report and literature reviewT L Williams, P J Shaw, J Lowe, et al.
Neurology|November 30, 2000
Relapsing ischemic encephaloenteropathy and cryoglobulinemiaP G Ince, P Duffey, H R Cochrane, et al.
Brain Research|February 21, 1994
N-methyl-D-aspartate (NMDA) receptors in the spinal cord and motor cortex in motor neuron disease: a quantitative autoradiographic study using [3H]MK-801P J Shaw, P G Ince, J N Matthews, et al.
Neuroreport|January 1, 1993
On the origin of Alzheimer's disease: a hypothesisG W Roberts, M Nash, P G Ince, et al.
Brain Research|July 2, 1993
Autoradiographic comparison of the distribution of [3H]MK801 and [3H]CNQX in the human cerebellum during development and agingM Johnson, E K Perry, P G Ince, et al.
Brain Research|February 14, 1992
The quantitative autoradiographic distribution of [3H]MK-801 binding sites in the normal human brainstem in relation to motor neuron diseaseP J Shaw, P G Ince, M Johnson, et al.
Journal of Neuropathology and Experimental Neurology|October 24, 1998
Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALSP G Ince, J Tomkins, J Y Slade, et al.
Pageof 14

Showing results (31-40 of 136) with videos related to

Sort By:
Pageof 14
Acta Neuropathologica|October 1, 1996
Familial amyotrophic lateral sclerosis with a mutation in exon 4 of the Cu/Zn superoxide dismutase gene: pathological and immunocytochemical changesP G Ince, P J Shaw, J Y Slade, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1991
Lower motor neuron degeneration and familial predisposition to colonic neoplasia in two adult siblingsP J Shaw, P G Ince, J Slade, et al.
Brain Research|January 18, 1991
The quantitative autoradiographic distribution of [3H]MK-801 binding sites in the normal human spinal cordP J Shaw, P G Ince, M Johnson, et al.
Acta Neuropathologica|January 1, 1995
Parkinsonism in motor neuron disease: case report and literature reviewT L Williams, P J Shaw, J Lowe, et al.
Neurology|November 30, 2000
Relapsing ischemic encephaloenteropathy and cryoglobulinemiaP G Ince, P Duffey, H R Cochrane, et al.
Brain Research|February 21, 1994
N-methyl-D-aspartate (NMDA) receptors in the spinal cord and motor cortex in motor neuron disease: a quantitative autoradiographic study using [3H]MK-801P J Shaw, P G Ince, J N Matthews, et al.
Neuroreport|January 1, 1993
On the origin of Alzheimer's disease: a hypothesisG W Roberts, M Nash, P G Ince, et al.
Brain Research|July 2, 1993
Autoradiographic comparison of the distribution of [3H]MK801 and [3H]CNQX in the human cerebellum during development and agingM Johnson, E K Perry, P G Ince, et al.
Brain Research|February 14, 1992
The quantitative autoradiographic distribution of [3H]MK-801 binding sites in the normal human brainstem in relation to motor neuron diseaseP J Shaw, P G Ince, M Johnson, et al.
Journal of Neuropathology and Experimental Neurology|October 24, 1998
Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALSP G Ince, J Tomkins, J Y Slade, et al.
Pageof 14