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Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution.
Shiga Y, Satoh K, Kitamoto T, Kanno S, Nakashima I, Sato S, Fujihara K, Takata H, Nobukuni K, Kuroda S, Takano H, Umeda Y, Konno H, Nagasato K, Satoh A, Matsuda Y, Hidaka M, Takahashi H, Sano Y, Kim K, Konishi T, Doh-ura K, Sato T, Sasaki K, Nakamura Y, Yamada M, Mizusawa H, Itoyama Y. Shiga Y, et al. Among authors: nobukuni k. J Neurol. 2007 Nov;254(11):1509-17. doi: 10.1007/s00415-007-0540-9. Epub 2007 Nov 2. J Neurol. 2007. PMID: 17965961
Coexistence of Creutzfeldt-Jakob disease, Lewy body disease, and Alzheimer's disease pathology: an autopsy case showing typical clinical features of Creutzfeldt-Jakob disease.
Haraguchi T, Terada S, Ishizu H, Sakai K, Tanabe Y, Nagai T, Takata H, Nobukuni K, Ihara Y, Kitamoto T, Kuroda S. Haraguchi T, et al. Among authors: nobukuni k. Neuropathology. 2009 Aug;29(4):454-9. doi: 10.1111/j.1440-1789.2008.00964.x. Neuropathology. 2009. PMID: 18715272 Review.
Creutzfeldt-Jakob disease with the M232R mutation in the prion protein gene in two cases showing different disease courses: a clinicopathological study.
Takeda N, Yokota O, Terada S, Haraguchi T, Nobukuni K, Mizuki R, Honda H, Yoshida H, Kishimoto Y, Oshima E, Ishizu H, Satoh K, Kitamoto T, Ihara Y, Uchitomi Y. Takeda N, et al. Among authors: nobukuni k. J Neurol Sci. 2012 Jan 15;312(1-2):108-16. doi: 10.1016/j.jns.2011.08.008. Epub 2011 Oct 7. J Neurol Sci. 2012. PMID: 21983261 Review.
Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and lewy body-like hyaline inclusions.
Takehisa Y, Ujike H, Ishizu H, Terada S, Haraguchi T, Tanaka Y, Nishinaka T, Nobukuni K, Ihara Y, Namba R, Yasuda T, Nishibori M, Hayabara T, Kuroda S. Takehisa Y, et al. Among authors: nobukuni k. Arch Neurol. 2001 May;58(5):736-40. doi: 10.1001/archneur.58.5.736. Arch Neurol. 2001. PMID: 11346368
41 results