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Brain : a Journal of Neurology|April 14, 2011
Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemiaAkio Yokoseki, Tomohiko Ishihara, Akihide Koyama, et al.
Acta Neuropathologica|February 9, 2010
Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entityYong-Juan Fu, Yasushi Nishihira, Shigetoshi Kuroda, et al.
Scientific Reports|January 23, 2026
ABCC6 pathogenic variants are associated with hemorrhagic phenotypes in Japanese patients with severe cerebral small vessel diseaseSho Kitahara, Shoichiro Ando, Masahiro Uemura, et al.
BMC Medical Genomics|November 7, 2024
SMN2 gene copy number affects the incidence and prognosis of motor neuron diseases in JapanTomohiko Ishihara, Akihide Koyama, Naoki Atsuta, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 19, 2022
High frequency of <i>HTRA1</i> AND <i>ABCC6</i> mutations in Japanese patients with adult-onset cerebral small vessel diseaseMasahiro Uemura, Yuya Hatano, Hiroaki Nozaki, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 15, 2023
Preclinical Characterization of the Tau PET Tracer [<sup>18</sup>F]SNFT-1: Comparison of Tau PET TracersRyuichi Harada, Pradith Lerdsirisuk, Yuki Shimizu, et al.
Neurobiology of Aging|January 18, 2022
Mutation screening of the DNAJC7 gene in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Naoki Atsuta, et al.
JMIR Research Protocols|December 23, 2018
The Japanese Early-Stage Trial of High-Dose Methylcobalamin for Amyotrophic Lateral Sclerosis (JETALS): Protocol for a Randomized Controlled TrialRyosuke Oki, Yuishin Izumi, Hiroyuki Nodera, et al.
Eclinicalmedicine|May 31, 2023
High-dose ubiquinol supplementation in multiple-system atrophy: a multicentre, randomised, double-blinded, placebo-controlled phase 2 trialJun Mitsui, Takashi Matsukawa, Yukari Uemura, et al.
Communications Biology|September 24, 2020
A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosisRyoichi Nakamura, Kazuharu Misawa, Genki Tohnai, et al.
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