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Characterization of IgG4 anti-neurofascin 155 antibody-positive polyneuropathy.
Ogata H, Yamasaki R, Hiwatashi A, Oka N, Kawamura N, Matsuse D, Kuwahara M, Suzuki H, Kusunoki S, Fujimoto Y, Ikezoe K, Kishida H, Tanaka F, Matsushita T, Murai H, Kira J. Ogata H, et al. Among authors: oka n. Ann Clin Transl Neurol. 2015 Oct;2(10):960-71. doi: 10.1002/acn3.248. Epub 2015 Sep 11. Ann Clin Transl Neurol. 2015. PMID: 26478896 Free PMC article.
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 patients.
Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G; Study Group for Hereditary Neuropathy in Japan. Hattori N, et al. Among authors: oka n. Brain. 2003 Jan;126(Pt 1):134-51. doi: 10.1093/brain/awg012. Brain. 2003. PMID: 12477701 Review.
ELectron microscopic abnormality and therapeutic efficacy in chronic inflammatory demyelinating polyneuropathy with anti-neurofascin155 immunoglobulin G4 antibody.
Kuwahara M, Suzuki H, Oka N, Ogata H, Yanagimoto S, Sadakane S, Fukumoto Y, Yamana M, Yuhara Y, Yoshikawa K, Morikawa M, Kawai S, Okazaki M, Tsujimoto T, Kira JI, Kusunoki S. Kuwahara M, et al. Among authors: oka n. Muscle Nerve. 2018 Mar;57(3):498-502. doi: 10.1002/mus.25757. Epub 2017 Aug 23. Muscle Nerve. 2018. PMID: 28796305
Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in Japan.
Inada R, Hirano M, Oka N, Samukawa M, Saigoh K, Suzuki H, Udaka F, Hashiguchi A, Takashima H, Hamada Y, Nakamura Y, Kusunoki S. Inada R, et al. Among authors: oka n. J Neurol. 2021 Aug;268(8):2933-2942. doi: 10.1007/s00415-021-10467-z. Epub 2021 Feb 24. J Neurol. 2021. PMID: 33625581
670 results