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Hidehiro Mizusawa

Showing results (221-230 of 302) with videos related to

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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 mappingA 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 cohortKokoro Ozaki, Ayaka Ansai, Kouji Nobuhara, et al.
Molecular Therapy. Nucleic Acids|January 14, 2015
Chimeric Antisense Oligonucleotide Conjugated to α-TocopherolTomoko 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 JapanTsuyoshi 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 lossZen 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 caseZen Kobayashi, Kuniaki Tsuchiya, Akira Machida, et al.
Neurobiology of Aging|February 19, 2014
Evaluation of polyglutamine repeats in autosomal dominant Parkinson's diseaseChikara 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 surveyShintaro 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 JapanMingshun 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 enzymeTakanori Yokota, Makoto Miyagishi, Taro Hino, et al.
Pageof 31

Showing results (221-230 of 302) with videos related to

Sort By:
Pageof 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 mappingA 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 cohortKokoro Ozaki, Ayaka Ansai, Kouji Nobuhara, et al.
Molecular Therapy. Nucleic Acids|January 14, 2015
Chimeric Antisense Oligonucleotide Conjugated to α-TocopherolTomoko 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 JapanTsuyoshi 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 lossZen 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 caseZen Kobayashi, Kuniaki Tsuchiya, Akira Machida, et al.
Neurobiology of Aging|February 19, 2014
Evaluation of polyglutamine repeats in autosomal dominant Parkinson's diseaseChikara 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 surveyShintaro 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 JapanMingshun 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 enzymeTakanori Yokota, Makoto Miyagishi, Taro Hino, et al.
Pageof 31