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Naohisa Ueda

Showing results (21-30 of 33) with videos related to

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Brain Communications|March 20, 2023
Reduced likelihood of the Poggendorff illusion in cerebellar strokes: a clinical and neuroimaging studyYuichi Higashiyama, Miho Kuroki, Yosuke Kudo, et al.
BMC Neurology|November 23, 2024
A case report of an individual with Creutzfeldt-Jakob disease characterized by prolonged isolated thalamic lesions and rare MM2-cortical-type pathologyMisako Kunii, Hitaru Kishida, Mikiko Tada, 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.
Brain : a Journal of Neurology|June 30, 2026
Two scripts, two pathways: dorsal-ventral biases in post-stroke kana-kanji agraphiaTakeshi Ito, Yuichi Higashiyama, Masayo Urano, et al.
Thrombosis Research|August 28, 2021
Therapeutic efficacy of heparin and direct factor Xa inhibitors in cancer-associated cryptogenic ischemic stroke with venous thromboembolismGenpei Yamaura, Takeshi Ito, Yosuke Miyaji, et al.
Journal of Human Genetics|February 6, 2015
A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutationMisako Kunii, Hiroshi Doi, Yuichi Higashiyama, 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.
Journal of Human Genetics|May 14, 2020
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in JapanYuanzhe Li, Aya Ikeda, Hiroyo Yoshino, et al.
Annals of Neurology|December 8, 2023
RNA Foci in Two bi-Allelic RFC1 Expansion CarriersTaishi Wada, Hiroshi Doi, Masaki Okubo, et al.
NPJ Genomic Medicine|October 26, 2022
Rapid and comprehensive diagnostic method for repeat expansion diseases using nanopore sequencingSatoko Miyatake, Eriko Koshimizu, Atsushi Fujita, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Brain Communications|March 20, 2023
Reduced likelihood of the Poggendorff illusion in cerebellar strokes: a clinical and neuroimaging studyYuichi Higashiyama, Miho Kuroki, Yosuke Kudo, et al.
BMC Neurology|November 23, 2024
A case report of an individual with Creutzfeldt-Jakob disease characterized by prolonged isolated thalamic lesions and rare MM2-cortical-type pathologyMisako Kunii, Hitaru Kishida, Mikiko Tada, 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.
Brain : a Journal of Neurology|June 30, 2026
Two scripts, two pathways: dorsal-ventral biases in post-stroke kana-kanji agraphiaTakeshi Ito, Yuichi Higashiyama, Masayo Urano, et al.
Thrombosis Research|August 28, 2021
Therapeutic efficacy of heparin and direct factor Xa inhibitors in cancer-associated cryptogenic ischemic stroke with venous thromboembolismGenpei Yamaura, Takeshi Ito, Yosuke Miyaji, et al.
Journal of Human Genetics|February 6, 2015
A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutationMisako Kunii, Hiroshi Doi, Yuichi Higashiyama, 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.
Journal of Human Genetics|May 14, 2020
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in JapanYuanzhe Li, Aya Ikeda, Hiroyo Yoshino, et al.
Annals of Neurology|December 8, 2023
RNA Foci in Two bi-Allelic RFC1 Expansion CarriersTaishi Wada, Hiroshi Doi, Masaki Okubo, et al.
NPJ Genomic Medicine|October 26, 2022
Rapid and comprehensive diagnostic method for repeat expansion diseases using nanopore sequencingSatoko Miyatake, Eriko Koshimizu, Atsushi Fujita, et al.
Pageof 4