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Movement Disorders : Official Journal of the Movement Disorder Society
|
June 5, 2003
Brain perfusion SPECT in patients with corticobasal degeneration: analysis using statistical parametric mapping
A K M Moinul Hossain, Yuji Murata, Lin Zhang, et al.
Parkinsonism & Related Disorders
|
May 21, 2019
Prevalence and clinicoradiological features of spinocerebellar ataxia type 34 in a Japanese ataxia cohort
Kokoro Ozaki, Ayaka Ansai, Kouji Nobuhara, et al.
Molecular Therapy. Nucleic Acids
|
January 14, 2015
Chimeric Antisense Oligonucleotide Conjugated to α-Tocopherol
Tomoko Nishina, Junna Numata, Kazutaka Nishina, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 19, 2013
Insight into the frequent occurrence of dura mater graft-associated Creutzfeldt-Jakob disease in Japan
Tsuyoshi Hamaguchi, Kenji Sakai, Moeko Noguchi-Shinohara, et al.
Journal of the Neurological Sciences
|
September 3, 2010
Clinicopathological characteristics of FTLD-TDP showing corticospinal tract degeneration but lacking lower motor neuron loss
Zen Kobayashi, Kuniaki Tsuchiya, Tetsuaki Arai, et al.
Journal of the Neurological Sciences
|
December 2, 2008
Metastatic CNS lymphoma presenting with periventricular dissemination - MRI and neuropathological findings in an autopsy case
Zen Kobayashi, Kuniaki Tsuchiya, Akira Machida, et al.
Neurobiology of Aging
|
February 19, 2014
Evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease
Chikara Yamashita, Hiroyuki Tomiyama, Manabu Funayama, et al.
Journal of Neurology
|
March 17, 2026
Prevalence and profiles of clinically diagnosed autoimmune cerebellar ataxia in a Japanese nationwide survey
Shintaro Fujii, Hiroaki Yaguchi, Akihiko Kudo, et al.
Journal of Human Genetics
|
March 8, 2003
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
Mingshun Li, Kinya Ishikawa, Shuta Toru, et al.
Biochemical and Biophysical Research Communications
|
January 13, 2004
siRNA-based inhibition specific for mutant SOD1 with single nucleotide alternation in familial ALS, compared with ribozyme and DNA enzyme
Takanori Yokota, Makoto Miyagishi, Taro Hino, et al.
Page
of 31
Search research articles
Search
Showing results (221-230 of 302) with videos related to
Sort By:
Page
of 31
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 5, 2003
Brain perfusion SPECT in patients with corticobasal degeneration: analysis using statistical parametric mapping
A K M Moinul Hossain, Yuji Murata, Lin Zhang, et al.
Parkinsonism & Related Disorders
|
May 21, 2019
Prevalence and clinicoradiological features of spinocerebellar ataxia type 34 in a Japanese ataxia cohort
Kokoro Ozaki, Ayaka Ansai, Kouji Nobuhara, et al.
Molecular Therapy. Nucleic Acids
|
January 14, 2015
Chimeric Antisense Oligonucleotide Conjugated to α-Tocopherol
Tomoko Nishina, Junna Numata, Kazutaka Nishina, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 19, 2013
Insight into the frequent occurrence of dura mater graft-associated Creutzfeldt-Jakob disease in Japan
Tsuyoshi Hamaguchi, Kenji Sakai, Moeko Noguchi-Shinohara, et al.
Journal of the Neurological Sciences
|
September 3, 2010
Clinicopathological characteristics of FTLD-TDP showing corticospinal tract degeneration but lacking lower motor neuron loss
Zen Kobayashi, Kuniaki Tsuchiya, Tetsuaki Arai, et al.
Journal of the Neurological Sciences
|
December 2, 2008
Metastatic CNS lymphoma presenting with periventricular dissemination - MRI and neuropathological findings in an autopsy case
Zen Kobayashi, Kuniaki Tsuchiya, Akira Machida, et al.
Neurobiology of Aging
|
February 19, 2014
Evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease
Chikara Yamashita, Hiroyuki Tomiyama, Manabu Funayama, et al.
Journal of Neurology
|
March 17, 2026
Prevalence and profiles of clinically diagnosed autoimmune cerebellar ataxia in a Japanese nationwide survey
Shintaro Fujii, Hiroaki Yaguchi, Akihiko Kudo, et al.
Journal of Human Genetics
|
March 8, 2003
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
Mingshun Li, Kinya Ishikawa, Shuta Toru, et al.
Biochemical and Biophysical Research Communications
|
January 13, 2004
siRNA-based inhibition specific for mutant SOD1 with single nucleotide alternation in familial ALS, compared with ribozyme and DNA enzyme
Takanori Yokota, Makoto Miyagishi, Taro Hino, et al.
Page
of 31