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Magnetic Resonance in Medical Sciences : MRMS : an Official Journal of Japan Society of Magnetic Resonance in Medicine|December 28, 2016
MR Spectroscopy in Patients with Hereditary Diffuse Leukoencephalopathy with Spheroids and Asymptomatic Carriers of Colony-stimulating Factor 1 Receptor MutationTakashi Abe, Toshitaka Kawarai, Koji Fujita, et al.Proceedings of the National Academy of Sciences of the United States of America|August 21, 2008
Differential involvement of striosome and matrix dopamine systems in a transgenic model of dopa-responsive dystoniaKenta Sato, Chiho Sumi-Ichinose, Ryuji Kaji, et al.Human Molecular Genetics|November 16, 2011
Parkin interacts with Klokin1 for mitochondrial import and maintenance of membrane potentialYukiko Kuroda, Wataru Sako, Satoshi Goto, et al.Scientific Data|October 15, 2024
Comprehensive data for studying serum exosome microRNA transcriptome in Parkinson's disease patientsZhiyang Yu, Shinji Saiki, Kenta Shiina, et al.Eneurologicalsci|February 24, 2018
Late-onset myasthenia gravis is predisposed to become generalized in the elderlyWaka Sakai, Naoko Matsui, Mitsuyo Ishida, et al.Movement Disorders Clinical Practice|November 13, 2025
Motor and Cognitive Outcome After Subthalamic Nucleus Deep Brain Stimulation in Patients with Parkinson's Disease Harboring GBA1 VariantHikaru Kamo, Genko Oyama, Mai Shimizu, et al.Journal of the Neurological Sciences|May 24, 2024
Safinamide as adjunctive therapy to levodopa monotherapy for patients with Parkinson's disease with wearing-off: The Japanese observational J-SILVER studyNoriko Nishikawa, Taku Hatano, Kenya Nishioka, et al.Journal of the Neurological Sciences|January 21, 2024
Free-water diffusion magnetic resonance imaging under selegiline treatment in Parkinson's diseaseHaruka Takeshige-Amano, Taku Hatano, Koji Kamagata, et al.Scientific Reports|February 9, 2026
Identification of perception gaps between physicians and patients with neurological diseases and the prediction of these gaps using machine learningGenko Oyama, Yuji Tomizawa, Taiji Tsunemi, et al.American Journal of Human Genetics|August 14, 2012
The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvementHiroyuki Ishiura, Wataru Sako, Mari Yoshida, et al.Pageof 8