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Journal of Vestibular Research : Equilibrium & Orientation|August 21, 2023
Visual fixation suppression of caloric nystagmus in progressive supranuclear palsy - A comparison with Parkinson's diseaseRie Naito, Yuki Watanabe, Akira Naito, et al.
Journal of Neurology|April 4, 2024
Pallidal deep brain stimulation for patients with myoclonus-dystonia without SGCE mutationsJun Ikezawa, Fusako Yokochi, Ryoichi Okiyama, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 29, 2025
Bilateral Effects of Unilateral Pallidothalamic Tractotomy Using Focused Ultrasound in Parkinson's DiseaseJun Ikezawa, Fusako Yokochi, Toshio Yamaguchi, et al.
Developmental Medicine and Child Neurology|October 31, 2014
Clinical and genetic investigation of 17 Japanese patients with hyperekplexiaJun Mine, Takeshi Taketani, Kazushi Yoshida, et al.
Archives of Neurology|June 11, 2008
Mutation analysis of the PINK1 gene in 391 patients with Parkinson diseaseRyuya Kumazawa, Hiroyuki Tomiyama, Yuanzhe Li, et al.
Parkinsonism & Related Disorders|April 15, 2018
Phenotype variability and allelic heterogeneity in KMT2B-Associated diseaseToshitaka Kawarai, Ryosuke Miyamoto, Eiji Nakagawa, et al.
Movement Disorders Clinical Practice|October 21, 2014
Official Japanese Version of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale: validation against the original English versionKenichi Kashihara, Tomoyoshi Kondo, Yoshikuni Mizuno, et al.
Brain : a Journal of Neurology|March 24, 2020
Variants in saposin D domain of prosaposin gene linked to Parkinson's diseaseYutaka Oji, Taku Hatano, Shin-Ichi Ueno, et al.
Plos One|November 14, 2013
Short and long term outcome of bilateral pallidal stimulation in chorea-acanthocytosisMarie Miquel, Umberto Spampinato, Chrystelle Latxague, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2011
Novel pathogenic mutations and copy number variations in the VPS13A gene in patients with chorea-acanthocytosisAkiyuki Tomiyasu, Masayuki Nakamura, Mio Ichiba, et al.
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