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Co-morbidity of progressive supranuclear palsy and amyotrophic lateral sclerosis: a clinical-pathological case report.
Fujita K, Matsubara T, Miyamoto R, Sumikura H, Takeuchi T, Maruyama Saladini K, Kawarai T, Nodera H, Udaka F, Kume K, Morino H, Kawakami H, Hasegawa M, Kaji R, Murayama S, Izumi Y. Fujita K, et al. Among authors: kaji r. BMC Neurol. 2019 Jul 18;19(1):168. doi: 10.1186/s12883-019-1402-7. BMC Neurol. 2019. PMID: 31319800 Free PMC article.
HNPP due to a novel missense mutation of the PMP22 gene.
Nodera H, Nishimura M, Logigian EL, Herrmann DN, Kaji R. Nodera H, et al. Among authors: kaji r. Neurology. 2003 Jun 10;60(11):1863-4. doi: 10.1212/01.wnl.0000066049.13848.f2. Neurology. 2003. PMID: 12796555 No abstract available.
Nerve excitability properties in Charcot-Marie-Tooth disease type 1A.
Nodera H, Bostock H, Kuwabara S, Sakamoto T, Asanuma K, Jia-Ying S, Ogawara K, Hattori N, Hirayama M, Sobue G, Kaji R. Nodera H, et al. Among authors: kaji r. Brain. 2004 Jan;127(Pt 1):203-11. doi: 10.1093/brain/awh020. Epub 2003 Nov 7. Brain. 2004. PMID: 14607794
652 results