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E Ohama

Showing results (121-130 of 132) with videos related to

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Acta Neurochirurgica|January 1, 1992
Problems related to dorsal root entry zone lesionsY Kumagai, K Shimoji, T Honma, et al.
Journal of the Neurological Sciences|June 1, 1990
Abnormal glycosphingolipid metabolism in the nervous system of galactosialidosisH Yoshino, K Miyashita, N Miyatani, et al.
Seishin Shinkeigaku Zasshi = Psychiatria Et Neurologia Japonica|January 1, 1990
[A clinical study and neuropathological findings of a familial disease with myoclonus and epilepsy--the nosological place of familial essential myoclonus and epilepsy (FEME)]G Inazuki, H Naito, E Ohama, et al.
Acta Neuropathologica|March 25, 1999
Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analysesS Kato, S Horiuchi, K Nakashima, et al.
Journal of the Neurological Sciences|September 1, 1989
Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)M Yoneda, M Tanaka, M Nishikimi, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 24, 2001
New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytesS Kato, M Takikawa, K Nakashima, et al.
Canadian Journal of Veterinary Research = Revue Canadienne De Recherche Veterinaire|February 23, 2002
Cliniconeuropathologic findings of familial frontal lobe epilepsy in Shetland sheepdogsT Morita, A Shimada, T Takeuchi, et al.
The Biochemical Journal|September 15, 1994
Human inositol 1,4,5-trisphosphate type-1 receptor, InsP3R1: structure, function, regulation of expression and chromosomal localizationN Yamada, Y Makino, R A Clark, et al.
Acta Neuropathologica|October 25, 2000
Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutationS Kato, S Horiuchi, J Liu, et al.
Science (New York, N.Y.)|September 22, 1998
Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1L I Bruijn, M K Houseweart, S Kato, et al.
Pageof 14

Showing results (121-130 of 132) with videos related to

Sort By:
Pageof 14
Acta Neurochirurgica|January 1, 1992
Problems related to dorsal root entry zone lesionsY Kumagai, K Shimoji, T Honma, et al.
Journal of the Neurological Sciences|June 1, 1990
Abnormal glycosphingolipid metabolism in the nervous system of galactosialidosisH Yoshino, K Miyashita, N Miyatani, et al.
Seishin Shinkeigaku Zasshi = Psychiatria Et Neurologia Japonica|January 1, 1990
[A clinical study and neuropathological findings of a familial disease with myoclonus and epilepsy--the nosological place of familial essential myoclonus and epilepsy (FEME)]G Inazuki, H Naito, E Ohama, et al.
Acta Neuropathologica|March 25, 1999
Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analysesS Kato, S Horiuchi, K Nakashima, et al.
Journal of the Neurological Sciences|September 1, 1989
Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)M Yoneda, M Tanaka, M Nishikimi, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 24, 2001
New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytesS Kato, M Takikawa, K Nakashima, et al.
Canadian Journal of Veterinary Research = Revue Canadienne De Recherche Veterinaire|February 23, 2002
Cliniconeuropathologic findings of familial frontal lobe epilepsy in Shetland sheepdogsT Morita, A Shimada, T Takeuchi, et al.
The Biochemical Journal|September 15, 1994
Human inositol 1,4,5-trisphosphate type-1 receptor, InsP3R1: structure, function, regulation of expression and chromosomal localizationN Yamada, Y Makino, R A Clark, et al.
Acta Neuropathologica|October 25, 2000
Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutationS Kato, S Horiuchi, J Liu, et al.
Science (New York, N.Y.)|September 22, 1998
Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1L I Bruijn, M K Houseweart, S Kato, et al.
Pageof 14