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O Onodera

Showing results (81-90 of 92) with videos related to

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Nature Genetics|October 1, 1995
Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's diseaseK Okuizumi, O Onodera, Y Namba, et al.
Neuropathology and Applied Neurobiology|October 11, 2019
Morphological characterisation of glial and neuronal tau pathology in globular glial tauopathy (Types II and III)H Tanaka, Y Toyoshima, S Kawakatsu, et al.
AJNR. American Journal of Neuroradiology|September 17, 2016
Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented GliaT Konno, D F Broderick, N Mezaki, et al.
Neurology|December 31, 1997
Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findingsR Koide, O Onodera, T Ikeuchi, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 26, 2008
[The clinical-genealogic and molecular-genetic characteristics of oculopharyngeal muscular dystrophy in the Republic of Sakha (Yakutia)]N R Maksimova, I A Nikolaeva, M N Korotkov, et al.
Neurology|May 12, 2004
Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B5H Ohtake, T Shimohata, K Terajima, et al.
Nature Genetics|October 5, 2001
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily geneH Date, O Onodera, H Tanaka, et al.
Neurology|April 27, 2005
Clinical and electrophysiologic correlates of IVIg responsiveness in CIDPM Iijima, M Yamamoto, M Hirayama, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 19, 2005
Age associated axonal features in HNPP with 17p11.2 deletion in JapanH Koike, M Hirayama, M Yamamoto, et al.
Neurology|September 15, 2004
Beta-synuclein gene alterations in dementia with Lewy bodiesH Ohtake, P Limprasert, Y Fan, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Nature Genetics|October 1, 1995
Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's diseaseK Okuizumi, O Onodera, Y Namba, et al.
Neuropathology and Applied Neurobiology|October 11, 2019
Morphological characterisation of glial and neuronal tau pathology in globular glial tauopathy (Types II and III)H Tanaka, Y Toyoshima, S Kawakatsu, et al.
AJNR. American Journal of Neuroradiology|September 17, 2016
Diagnostic Value of Brain Calcifications in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented GliaT Konno, D F Broderick, N Mezaki, et al.
Neurology|December 31, 1997
Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findingsR Koide, O Onodera, T Ikeuchi, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|June 26, 2008
[The clinical-genealogic and molecular-genetic characteristics of oculopharyngeal muscular dystrophy in the Republic of Sakha (Yakutia)]N R Maksimova, I A Nikolaeva, M N Korotkov, et al.
Neurology|May 12, 2004
Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B5H Ohtake, T Shimohata, K Terajima, et al.
Nature Genetics|October 5, 2001
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily geneH Date, O Onodera, H Tanaka, et al.
Neurology|April 27, 2005
Clinical and electrophysiologic correlates of IVIg responsiveness in CIDPM Iijima, M Yamamoto, M Hirayama, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 19, 2005
Age associated axonal features in HNPP with 17p11.2 deletion in JapanH Koike, M Hirayama, M Yamamoto, et al.
Neurology|September 15, 2004
Beta-synuclein gene alterations in dementia with Lewy bodiesH Ohtake, P Limprasert, Y Fan, et al.
Pageof 10