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Journal of Neurology|February 24, 2021
Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in JapanRino Inada, Makito Hirano, Nobuyuki Oka, et al.
Journal of Neuroimmunology|December 28, 2025
The activation of classical and/or lectin complement pathway for the pathogenesis of chronic inflammatory demyelinating polyradiculoneuropathyKeishu Murakami, Hiroshi Tsujimoto, Yoshiaki Nakayama, et al.
Brain : a Journal of Neurology|March 26, 2002
Chemokines and chemokine receptors in inflammatory demyelinating neuropathies: a central role for IP-10Bernd C Kieseier, Marie Tani, Don Mahad, et al.
Journal of Human Genetics|December 8, 2017
Charcot-Marie-Tooth disease type 2A with an autosomal-recessive inheritance: the first report of an adult-onset diseaseRyota Hikiami, Hirofumi Yamashita, Natsuko Koita, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|March 22, 2021
Eosinophil ETosis-Mediated Release of Galectin-10 in Eosinophilic Granulomatosis With PolyangiitisMineyo Fukuchi, Yosuke Kamide, Shigeharu Ueki, et al.
Scientific Reports|October 18, 2023
CANVAS-related RFC1 mutations in patients with immune-mediated neuropathyMakito Hirano, Motoi Kuwahara, Yuko Yamagishi, et al.
Frontiers in Immunology|January 31, 2022
Increased Circulating Cell-Free DNA in Eosinophilic Granulomatosis With Polyangiitis: Implications for Eosinophil Extracellular Traps and ImmunothrombosisTeppei Hashimoto, Shigeharu Ueki, Yosuke Kamide, et al.
Muscle & Nerve|August 11, 2017
ELectron microscopic abnormality and therapeutic efficacy in chronic inflammatory demyelinating polyneuropathy with anti-neurofascin155 immunoglobulin G4 antibodyMotoi Kuwahara, Hidekazu Suzuki, Nobuyuki Oka, et al.
Annals of Clinical and Translational Neurology|October 20, 2015
Characterization of IgG4 anti-neurofascin 155 antibody-positive polyneuropathyHidenori Ogata, Ryo Yamasaki, Akio Hiwatashi, et al.
Brain : a Journal of Neurology|December 13, 2002
Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patientsNaoki Hattori, Masahiko Yamamoto, Tsuyoshi Yoshihara, et al.
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