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Citation: M. Nakagawa et al., Phenotypic variation in a large Japanese family with Miyoshi myopathy withnonsense mutation in exon 19 of dysferlin gene, J NEUR SCI, 184(1), 2001, pp. 15-19

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Citation: N. Kanzato et al., Preserved sympathetic skin response at the distal phalanx in patients withcarpal tunnel syndrome, CLIN NEU, 111(11), 2000, pp. 2057-2063

Authors: Kanzato, N Motomura, M Suehara, M Arimura, K

Citation: N. Kanzato et al., Lambert-Eaton myasthenic syndrome with ophthalmoparesis and pseudoblepharospasm, MUSCLE NERV, 22(12), 1999, pp. 1727-1730

Authors: Nakagawa, M Suehara, M Saito, A Takashima, H Umehara, F Saito, M Kanzato, N Matsuzaki, T Takenaga, S Sakoda, S Izumo, S Osame, M

Citation: M. Nakagawa et al., A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths, NEUROLOGY, 52(6), 1999, pp. 1271-1275

Authors: Kanzato, N Matsuzaki, T Komine, Y Saito, M Saito, A Yoshio, T Suehara, M

Citation: N. Kanzato et al., Localized scleroderma associated with progressing ischemic stroke, J NEUR SCI, 163(1), 1999, pp. 86-89

Authors: Kanzato, N Saito, M Horikiri, T Komine, Y Nakagawa, M Matsuzaki, T

Citation: N. Kanzato et al., Atypical rigid form of Huntington's disease: A case with peripheral amyotrophy and congenital defects of a lower limb, INTERN MED, 37(11), 1998, pp. 978-981