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66 results for 運動失調

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運動失調を伴う急性期脳卒中患者における退院先を予測する至適尺度: SARA，FIM，BBS，FACTとの比較
Author / Creator:吉川, 昌太 ; 伊藤, 英隆 ; 長野, 聖
Publisher:Tokyo: 理学療法科学学会
Journal title:理学療法科学, 2018, Vol.33(2), pp.251-254
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Active vision indicator (AVI) を用いた介入により上肢の運動失調症状が軽減した小脳梗塞の一症例
Author / Creator:海津陽一 ; 宮田一弘
Publisher:理学療法科学学会
Journal title:理学療法科学, 2019-02, Vol.34 (1), p.149-153
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歩行変動性とバランス評価により運動療法を検討し歩行能力が向上した脳卒中後に運動失調を呈した一症例
Author / Creator:山崎, 雄一郎 ; 新井, 智之 ; 高石, 真二郎 ; 髙村, 浩司 ; 丸木, 秀行
Publisher:理学療法科学学会
Journal title:理学療法科学, 2022, Vol.37(1), pp.117-122
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Core stability trainingにより運動失調およびバランス障害が改善した重度小脳性および感覚性運動失調の1症例
Author / Creator:阪本, 誠 ; 松木, 明好 ; 谷, 恵介 ; 木村, 大輔
Publisher:Tokyo: 理学療法科学学会
Journal title:理学療法科学, 2017, Vol.32(3), pp.459-464
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Active vision indicator（AVI）を用いた介入により上肢の運動失調症状が軽減した小脳梗塞の一症例
Author / Creator:海津, 陽一 ; 宮田, 一弘
Publisher:Tokyo: 理学療法科学学会
Journal title:理学療法科学, 2019, Vol.34(1), pp.149-153
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ArticlesPeer ReviewedFull Text
双手活动不利行走不稳声音嘶哑
Author / Creator:乔晓会乔雷彭斌崔丽英
Publisher:100730,中国医学科学院北京协和医学院北京协和医院神经科
Journal title:中国现代神经疾病杂志, 2013, Vol.13 (3), p.250-254
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ArticlesPeer ReviewedFull Text
芳香族L-胺基酸脫羧基酶（AADC）缺乏症孩童進行基因轉殖之圍術期麻醉照護
Author / Creator:李文君(Wen-Chun LI) ; 范守仁(Shou-Zen FAN)
Publisher:台灣: 台灣護理學會
Journal title:護理雜誌, 2019-02, Vol.66 (1), p.107-114
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ArticlesPeer ReviewedFull Text
體感式電玩介入對慢性思覺失調症病人健康體適能之成效
Author / Creator:吳玉茹(Yu-Ju Wu) ; 蔡芸芳(Yun-Fang Tsai) ; 吳文正(Wen-Cheng Wu) ; 王鐘賢(Jong-Shyan Wang)
Publisher:台灣: 台灣護理學會
Journal title:護理雜誌, 2016-02, Vol.63 (1), p.49-58
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ArticlesPeer ReviewedFull Text
不宁腿综合征
Author / Creator:吴伟薛蓉
Publisher:300052,天津医科大学总医院神经内科
Journal title:中国现代神经疾病杂志, 2013, Vol.13 (5), p.387-391
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ArticlesPeer ReviewedFull Text
RFC1 repeat expansion in Japanese patients with late-onset cerebellar ataxia
Author / Creator:Tsuchiya, Mai ; Nan, Haitian ; Koh, Kishin ; Ichinose, Yuta ; Gao, Lihua ; Shimozono, Keisuke ; Hata, Takanori ; Kim, Yeon-Jeong ; Ohtsuka, Toshihisa ; Cortese, Andrea ; Takiyama, Yoshihisa
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2020-12, Vol.65 (12), p.1143-1147
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ArticlesPeer ReviewedFull Text
Compound heterozygous variants of THG1L result in autosomal recessive cerebellar ataxia
Author / Creator:Han, Rui ; Chu, Manman ; Gao, Jinshuang ; Wang, Junling ; Wang, Mengyue ; Ma, Yichao ; Jia, Tianming ; Zhang, Xiaoli
Publisher:London: Nature Publishing Group
Journal title:Journal of human genetics, 2023-12, Vol.68 (12), p.843-848
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A novel SLC9A1 mutation causes cerebellar ataxia
Author / Creator:Iwama, Kazuhiro ; Osaka, Hitoshi ; Ikeda, Takahiro ; Mitsuhashi, Satomi ; Miyatake, Satoko ; Takata, Atsushi ; Miyake, Noriko ; Ito, Shuichi ; Mizuguchi, Takeshi ; Matsumoto, Naomichi
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2018-10, Vol.63 (10), p.1049-1054
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Comparison of two families with and without ataxia harboring novel variants in PRKCG
Author / Creator:Tada, Yui ; Kume, Kodai ; Noguchi, Soma ; Sekiya, Tomoko ; Nishinaka, Kazuto ; Ishiguchi, Hiroshi ; Koh, Jinsoo ; Emori, Seiji ; Nakayama, Yoshiaki ; Kurashige, Takashi ; Izumi, Yuishin ; Ito, Hidefumi ; Sakai, Norio ; Kawakami, Hideshi
Publisher:London: Nature Publishing Group
Journal title:Journal of human genetics, 2022-10, Vol.67 (10), p.595-599
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Late-onset episodic ataxia associated with SLC1A3 mutation
Author / Creator:Choi, Kwang-Dong ; Jen, Joanna C ; Choi, Seo Young ; Shin, Jin-Hong ; Kim, Hyang-Sook ; Kim, Hyo-Jung ; Kim, Ji-Soo ; Choi, Jae-Hwan
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2017-03, Vol.62 (3), p.443-446
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Overwhelming genetic heterogeneity and exhausting molecular diagnostic process in chronic and progressive ataxias: facing it up with an algorithm, a gene, a panel at a time
Author / Creator:Perez Maturo, J. ; Zavala, L. ; Vega, P. ; González-Morón, D. ; Medina, N. ; Salinas, V. ; Rosales, J. ; Córdoba, M. ; Arakaki, T. ; Garretto, N. ; Rodríguez-Quiroga, S. ; Kauffman, M. A.
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2020-10, Vol.65 (10), p.895-902
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ArticlesPeer ReviewedFull Text
A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy
Author / Creator:Nasca, Alessia ; Di Meo, Ivano ; Fellig, Yakov ; Saada, Ann ; Elpeleg, Orly ; Ghezzi, Daniele ; Edvardson, Shimon
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2021-08, Vol.66 (8), p.835-840
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Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia–telangiectasia caused by novel compound heterozygous variants in ATM
Author / Creator:Sato, Daichi ; Moriya, Kunihiko ; Nakano, Tomohiro ; Miyagawa, Chihiro ; Katayama, Saori ; Niizuma, Hidetaka ; Sasahara, Yoji ; Kure, Shigeo
Publisher:Singapore: Springer Singapore
Journal title:International journal of hematology, 2021-12, Vol.114 (6), p.735-741
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Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment
Author / Creator:Koh, Kishin ; Ishiura, Hiroyuki ; Beppu, Minako ; Shimazaki, Haruo ; Ichinose, Yuta ; Mitsui, Jun ; Kuwabara, Satoshi ; Tsuji, Shoji ; Takiyama, Yoshihisa
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2018-09, Vol.63 (9), p.1009-1013
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ArticlesPeer ReviewedFull Text
Ataxia–telangiectasia mutated kinase‐mediated upregulation of NKG2D ligands on leukemia cells by resveratrol results in enhanced natural killer cell susceptibility
Author / Creator:Luis Espinoza, J. ; Takami, Akiyoshi ; Trung, Ly Q. ; Nakao, Shinji
Publisher:England: John Wiley and Sons Inc
Journal title:Cancer science, 2013-06, Vol.104 (6), p.657-662
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Episodic ataxia type 2 with a novel missense variant (Leu602Arg) in CACNA1A
Author / Creator:Miura, Shiroh ; Watanabe, Emina ; Senzaki, Kensuke ; Hiruki, Shigeyoshi ; Matsumoto, Sayaka ; Morikawa, Takuya ; Uchiyama, Yusuke ; Kurata, Seiji ; Ochi, Masayuki ; Ohyagi, Yasumasa ; Shibata, Hiroki
Publisher:London: Nature Publishing Group UK
Journal title:Human genome variation, 2024-01, Vol.11 (1), p.3-3, Article 3
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運動失調を伴う急性期脳卒中患者における退院先を予測する至適尺度: SARA，FIM，BBS，FACTとの比較

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Active vision indicator (AVI) を用いた介入により上肢の運動失調症状が軽減した小脳梗塞の一症例

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歩行変動性とバランス評価により運動療法を検討し歩行能力が向上した脳卒中後に運動失調を呈した一症例

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Core stability trainingにより運動失調およびバランス障害が改善した重度小脳性および感覚性運動失調の1症例

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Active vision indicator（AVI）を用いた介入により上肢の運動失調症状が軽減した小脳梗塞の一症例

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双手活动不利行走不稳声音嘶哑

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芳香族L-胺基酸脫羧基酶（AADC）缺乏症孩童進行基因轉殖之圍術期麻醉照護

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體感式電玩介入對慢性思覺失調症病人健康體適能之成效

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不宁腿综合征

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RFC1 repeat expansion in Japanese patients with late-onset cerebellar ataxia

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Compound heterozygous variants of THG1L result in autosomal recessive cerebellar ataxia

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A novel SLC9A1 mutation causes cerebellar ataxia

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Comparison of two families with and without ataxia harboring novel variants in PRKCG

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Late-onset episodic ataxia associated with SLC1A3 mutation

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Overwhelming genetic heterogeneity and exhausting molecular diagnostic process in chronic and progressive ataxias: facing it up with an algorithm, a gene, a panel at a time

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A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy

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Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia–telangiectasia caused by novel compound heterozygous variants in ATM

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Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment

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Ataxia–telangiectasia mutated kinase‐mediated upregulation of NKG2D ligands on leukemia cells by resveratrol results in enhanced natural killer cell susceptibility

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Episodic ataxia type 2 with a novel missense variant (Leu602Arg) in CACNA1A

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