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Hidehiro Mizusawa

Showing results (271-280 of 302) with videos related to

Pageof 31
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Rinsho Shinkeigaku = Clinical Neurology|June 23, 2017
Questionnaire survey on the process of specialty training in neurology in JapanMasahiro Sonoo, Kazutoshi Nishiyama, Tetsuo Ando, et al.
American Journal of Human Genetics|November 3, 2009
Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)nNozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, et al.
Neuron|March 28, 2017
Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31Taro Ishiguro, Nozomu Sato, Morio Ueyama, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 6, 2014
Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansionMasato Obayashi, Giovanni Stevanin, Matthis Synofzik, et al.
Journal of the Neurological Sciences|September 21, 2013
Pathological features of FTLD-FUS in a Japanese population: analyses of nine casesZen Kobayashi, Ito Kawakami, Tetsuaki Arai, et al.
Nature Communications|August 11, 2015
DNA/RNA heteroduplex oligonucleotide for highly efficient gene silencingKazutaka Nishina, Wenying Piao, Kie Yoshida-Tanaka, et al.
JAMA Neurology|May 27, 2015
A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34Kokoro Ozaki, Hiroshi Doi, Jun Mitsui, et al.
Neurology|February 15, 2018
Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia [RETIRED]: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of NeurologyTheresa A Zesiewicz, George Wilmot, Sheng-Han Kuo, et al.
Biomarker Research|October 12, 2017
Re-evaluation of soluble APP-α and APP-β in cerebrospinal fluid as potential biomarkers for early diagnosis of dementia disordersWataru Araki, Kotaro Hattori, Kazutomi Kanemaru, et al.
Brain : a Journal of Neurology|January 19, 2012
Non-human primate model of amyotrophic lateral sclerosis with cytoplasmic mislocalization of TDP-43Azusa Uchida, Hiroki Sasaguri, Nobuyuki Kimura, et al.
Pageof 31

Showing results (271-280 of 302) with videos related to

Sort By:
Pageof 31
Rinsho Shinkeigaku = Clinical Neurology|June 23, 2017
Questionnaire survey on the process of specialty training in neurology in JapanMasahiro Sonoo, Kazutoshi Nishiyama, Tetsuo Ando, et al.
American Journal of Human Genetics|November 3, 2009
Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)nNozomu Sato, Takeshi Amino, Kazuhiro Kobayashi, et al.
Neuron|March 28, 2017
Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31Taro Ishiguro, Nozomu Sato, Morio Ueyama, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 6, 2014
Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansionMasato Obayashi, Giovanni Stevanin, Matthis Synofzik, et al.
Journal of the Neurological Sciences|September 21, 2013
Pathological features of FTLD-FUS in a Japanese population: analyses of nine casesZen Kobayashi, Ito Kawakami, Tetsuaki Arai, et al.
Nature Communications|August 11, 2015
DNA/RNA heteroduplex oligonucleotide for highly efficient gene silencingKazutaka Nishina, Wenying Piao, Kie Yoshida-Tanaka, et al.
JAMA Neurology|May 27, 2015
A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34Kokoro Ozaki, Hiroshi Doi, Jun Mitsui, et al.
Neurology|February 15, 2018
Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia [RETIRED]: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of NeurologyTheresa A Zesiewicz, George Wilmot, Sheng-Han Kuo, et al.
Biomarker Research|October 12, 2017
Re-evaluation of soluble APP-α and APP-β in cerebrospinal fluid as potential biomarkers for early diagnosis of dementia disordersWataru Araki, Kotaro Hattori, Kazutomi Kanemaru, et al.
Brain : a Journal of Neurology|January 19, 2012
Non-human primate model of amyotrophic lateral sclerosis with cytoplasmic mislocalization of TDP-43Azusa Uchida, Hiroki Sasaguri, Nobuyuki Kimura, et al.
Pageof 31