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Yaeko Ichikawa

Showing results (21-30 of 38) with videos related to

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Journal of Human Genetics|July 12, 2002
Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseasesMasaji Tachikawa, Yoshitaka Nagai, Koichiro Nakamura, et al.
Archives of Neurology|May 29, 2012
C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of JapanHiroyuki Ishiura, Yuji Takahashi, Jun Mitsui, et al.
Frontiers in Neuroscience|April 5, 2021
Time Distortion in ParkinsonismYasuo Terao, Motoyasu Honma, Yuki Asahara, et al.
Journal of Molecular Neuroscience : MN|January 12, 2021
Cerebellar Ataxia as a Common Clinical Presentation Associated with DNMT1 p.Y511H and a Review of the LiteratureJunko Kanda Kikuchi, Yu Nagashima, Tatsuo Mano, et al.
Journal of Human Genetics|January 24, 2014
Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analysesHiroyuki Ishiura, Yuji Takahashi, Toshihiro Hayashi, et al.
Annals of Neurology|January 26, 2012
Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth diseaseMeiko Hashimoto Maeda, Jun Mitsui, Bing-Wen Soong, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 19, 2023
Roles of the cerebellum and basal ganglia in temporal integration: Insights from a synchronized tapping taskShin-Ichi Tokushige, Shunichi Matsuda, Masayoshi Tada, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 3, 2025
Novel in-frame duplication variant of <i>SOD1</i> in a Japanese family with familial amyotrophic lateral sclerosisMasanori Nakajima, Hiroya Naruse, Yuichi Riku, et al.
Neurology. Genetics|April 12, 2016
Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrumKagari Koshi Mano, Takashi Matsukawa, Jun Mitsui, et al.
Annals of Neurology|January 3, 2013
Mutations in KCND3 cause spinocerebellar ataxia type 22Yi-Chung Lee, Alexandra Durr, Karen Majczenko, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Journal of Human Genetics|July 12, 2002
Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseasesMasaji Tachikawa, Yoshitaka Nagai, Koichiro Nakamura, et al.
Archives of Neurology|May 29, 2012
C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of JapanHiroyuki Ishiura, Yuji Takahashi, Jun Mitsui, et al.
Frontiers in Neuroscience|April 5, 2021
Time Distortion in ParkinsonismYasuo Terao, Motoyasu Honma, Yuki Asahara, et al.
Journal of Molecular Neuroscience : MN|January 12, 2021
Cerebellar Ataxia as a Common Clinical Presentation Associated with DNMT1 p.Y511H and a Review of the LiteratureJunko Kanda Kikuchi, Yu Nagashima, Tatsuo Mano, et al.
Journal of Human Genetics|January 24, 2014
Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analysesHiroyuki Ishiura, Yuji Takahashi, Toshihiro Hayashi, et al.
Annals of Neurology|January 26, 2012
Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth diseaseMeiko Hashimoto Maeda, Jun Mitsui, Bing-Wen Soong, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 19, 2023
Roles of the cerebellum and basal ganglia in temporal integration: Insights from a synchronized tapping taskShin-Ichi Tokushige, Shunichi Matsuda, Masayoshi Tada, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 3, 2025
Novel in-frame duplication variant of <i>SOD1</i> in a Japanese family with familial amyotrophic lateral sclerosisMasanori Nakajima, Hiroya Naruse, Yuichi Riku, et al.
Neurology. Genetics|April 12, 2016
Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrumKagari Koshi Mano, Takashi Matsukawa, Jun Mitsui, et al.
Annals of Neurology|January 3, 2013
Mutations in KCND3 cause spinocerebellar ataxia type 22Yi-Chung Lee, Alexandra Durr, Karen Majczenko, et al.
Pageof 4