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A case report of an individual with Creutzfeldt-Jakob disease characterized by prolonged isolated thalamic lesions and rare MM2-cortical-type pathology.
Kunii M, Kishida H, Tada M, Okamoto M, Asano K, Nakamura H, Takahashi K, Hashiguchi S, Kubota S, Okubo M, Takeuchi H, Ueda N, Satoh K, Kitamoto T, Doi H, Tanaka F. Kunii M, et al. Among authors: satoh k. BMC Neurol. 2024 Nov 22;24(1):456. doi: 10.1186/s12883-024-03958-9. BMC Neurol. 2024. PMID: 39578797 Free PMC article.
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: satoh k, satoh a. J Neurol. 2007 Nov;254(11):1509-17. doi: 10.1007/s00415-007-0540-9. Epub 2007 Nov 2. J Neurol. 2007. PMID: 17965961
Decreased regional cerebral blood flow in the bilateral thalami and medulla oblongata determined by an easy Z-score (eZIS) analysis of (99m)Tc-ECD-SPECT images in a case of MM2-thalamic-type sporadic Creutzfeldt-Jakob disease.
Hayashi Y, Iwasaki Y, Yoshikura N, Asano T, Hatano T, Tatsumi S, Satoh K, Kimura A, Kitamoto T, Yoshida M, Inuzuka T. Hayashi Y, et al. Among authors: satoh k. J Neurol Sci. 2015 Nov 15;358(1-2):447-52. doi: 10.1016/j.jns.2015.09.356. Epub 2015 Sep 25. J Neurol Sci. 2015. PMID: 26421831
[Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course].
Takayanagi M, Suzuki K, Nakamura T, Hirata K, Satoh K, Kitamoto T. Takayanagi M, et al. Among authors: satoh k. Rinsho Shinkeigaku. 2018 Nov 28;58(11):682-687. doi: 10.5692/clinicalneurol.cn-001206. Epub 2018 Oct 27. Rinsho Shinkeigaku. 2018. PMID: 30369528 Japanese.
Clinicopathological findings of an MM2-cortical-type sporadic Creutzfeldt-Jakob disease patient with cortical blindness during a course of glaucoma and age-related macular degeneration.
Hayashi Y, Iwasaki Y, Waza M, Shibata H, Akagi A, Kimura A, Inuzuka T, Satoh K, Kitamoto T, Yoshida M, Shimohata T. Hayashi Y, et al. Among authors: satoh k. Prion. 2019 Jan;13(1):124-131. doi: 10.1080/19336896.2019.1631680. Prion. 2019. PMID: 31219399 Free PMC article.
3,199 results