Nishioka Kenya

Nishioka Kenya | Nishioka Kenya

Affiliation and department：
Job title： Associate Professor

Research field (1)： Neuroscience - general

Research keywords (6)： Clinical Neurology , Chronic pain , Clinical genetics , Hereditary leukoencephalopathy , Dementia , Parkinson disease

Research theme for competitive and other funds (5)：

2020 - 2023 Aim to identify a novel gene related to familial Parkinson's disease
2016 - 2019 Aim to detect a novel pathogenic mutation in a familial Parkinson's disease
2014 - 2017 Clinical Analysis of Neurodegenerative Dementia Using Cerebrospinal Fluid Biomarkers
2013 - 2017 The detection of modifier gens in alpha-synuclein multiplications
2013 - 2015 若手研究(B)

Papers (151)：

Noriko Nishikawa, Taku Hatano, Kenya Nishioka, Shin-Ichi Ueno, Shinji Saiki, Ryota Nakamura, Asako Yoritaka, Takashi Ogawa, Yasushi Shimo, Wataru Sako, et al. Safinamide as adjunctive therapy to levodopa monotherapy for patients with Parkinson's disease with wearing-off: The Japanese observational J-SILVER study. Journal of the neurological sciences. 2024. 461. 123051-123051
Kei-ichi Ishikawa, Takahiro Shiga, Hiroyo Yoshino, Kenya Nishioka, Nobutaka Hattori, Wado Akamatsu. Generation of three clones (JUCGRMi002-A, B, C) of induced pluripotent stem cells from a Parkinson’s disease patient with SNCA duplication. Stem Cell Research. 2024
Kensuke Daida, Manabu Funayama, Kimberley J Billingsley, Laksh Malik, Abigail Miano-Burkhardt, Hampton L Leonard, Mary B Makarious, Hirotaka Iwaki, Jinhui Ding, J Raphael Gibbs, et al. Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease. Movement disorders : official journal of the Movement Disorder Society. 2023. 38. 12. 2249-2257
Kensuke Daida, Manabu Funayama, Kimberley J Billingsley, Laksh Malik, Abigail Miano-Burkhardt, Hampton L Leonard, Mary B Makarious, Hirotaka Iwaki, Jinhui Ding, J Raphael Gibbs, et al. Long-read sequencing resolves a complex structural variant in PRKN Parkinson's disease. medRxiv : the preprint server for health sciences. 2023
Hajime Yasuda, Yoshiki Furukawa, Kenya Nishioka, Makoto Sasaki, Yutaka Tsukune, Shuichi Shirane, Nobutaka Hattori, Miki Ando, Norio Komatsu. Vitamin B6 deficiency as a cause of polyneuropathy in POEMS syndrome: rapid recovery with supplementation in two cases. Hematology (Amsterdam, Netherlands). 2022. 27. 1. 463-468

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MISC (64)：

西岡健弥, 山下由莉, 互健二, 島田斉, 吉野浩代, 李元哲, 舩山学, 舩山学, 樋口真, 服部信孝, et al. 新規変異MAPT p.K298_H299insQのタウイメージングと臨床遺伝学的解析. 日本人類遺伝学会大会プログラム・抄録集. 2021. 66th
王子悠, 波田野琢, 上野真一, 舩山学, 石川景一, 石川景一, 奥住文美, 野田幸子, 佐藤栄人, 李元哲, et al. プロサポシン遺伝子サポシンD領域変異によるパーキンソン病. パーキンソン病・運動障害疾患コングレスプログラム・抄録集. 2021. 14th
三嶋崇靖, 藤岡伸助, 佐藤和則, 保前英希, 矢部一郎, 塩見一剛, 西岡健弥, 波田野琢, 服部信孝, 坪井義夫. 日本におけるPerry病の特徴. 日本神経学会学術大会プログラム・抄録集. 2020. 61st
Masashi Takanashi, Manabu Funayama, Kenya Nishioka, Daisuke Taniguchi, Takashi Ogawa, Sho Tsuyama, Nobutaka Hattori. Isolated nigral degeneration not associated with a-synuclein pathologies in the familial Parkinson's disease with LRRK2 p.R1441H mutation. BRAIN PATHOLOGY. 2019. 29. 92-92
田中淳, 飯田紘太郎, 林田有沙, 西岡健弥, 服部信孝, 原英夫. VPS13C遺伝子変異を認めた家族性パーキンソン病の1例. 臨床神経学. 2018. 58. 8. 545-545

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Education (7)：

2022 - 現在 Department of Neurology, Juntendo Tokyo Koto Geriatric Medical Center
2013 - 現在 Juntendo University School of Medicine Medicine Neurology
2010 - 2013 Juntendo Urayasu Hospital Medicine Neurology
2008 - 2009 Mayo Clinic Jacksonville Department of Neuroscience
2004 - 2007 Graduate School of Medicine, Juntendo University School of Medicine Medicine Neurology

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Association Membership(s) (5)：

Genetic epidemiology of Parkinson's disease , Japan College of Fibromyalgia Investigation , The Japan Stroke Society , The Japanese Society of Internal Medicine , Japanese Society of Neurology

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