Nagasaka T - Search Results

1

[Clinical features of neuroferritinopathy].

Ohta E, Nagasaka T, Shindo K, Toma S, Nagasaka K, Miwa M, Takiyama Y, Shiozawa Z. Ohta E, et al. Among authors: nagasaka k, nagasaka t. Rinsho Shinkeigaku. 2009 May;49(5):254-61. doi: 10.5692/clinicalneurol.49.254. Rinsho Shinkeigaku. 2009. PMID: 19594102 Review. Japanese.

2

[Atypical distribution of muscular atrophy in a 29-year-old man with polymyositis and anti-SRP antibodies].

Miwa M, Nakamura Y, Nagasaka T, Shindo K, Takiyama Y. Miwa M, et al. Among authors: nagasaka t. Rinsho Shinkeigaku. 2012;52(4):234-8. doi: 10.5692/clinicalneurol.52.234. Rinsho Shinkeigaku. 2012. PMID: 22531655 Japanese.

3

[A case of cryptococcal ventriculitis with slowly progressive gait disturbance and memory impairment as initial symptoms].

Yamashiro N, Nagasaka T, Takaki R, Miwa M, Shindo K, Takiyama Y. Yamashiro N, et al. Among authors: nagasaka t. Rinsho Shinkeigaku. 2015;55(2):81-6. doi: 10.5692/clinicalneurol.55.81. Rinsho Shinkeigaku. 2015. PMID: 25746069 Review. Japanese.

4

[A case of Creutzfeldt-Jakob disease with a double mutation (V180I/M232R) in the PRNP gene].

Koh K, Takaki R, Miwa M, Nagasaka T, Shindo K, Takiyama Y. Koh K, et al. Among authors: nagasaka t. Rinsho Shinkeigaku. 2015;55(6):424-7. doi: 10.5692/clinicalneurol.cn-000646. Rinsho Shinkeigaku. 2015. PMID: 26103817 Japanese.

5

[A case of local tetanus presenting spastic paraplegia mimicking myelitis].

Tsuchiya M, Kobayashi F, Yamashiro N, Nagasaka T, Shindo K, Takiyama Y. Tsuchiya M, et al. Among authors: nagasaka t. Rinsho Shinkeigaku. 2018 Nov 28;58(11):688-691. doi: 10.5692/clinicalneurol.cn-001196. Epub 2018 Oct 27. Rinsho Shinkeigaku. 2018. PMID: 30369524 Japanese.

6

[A case of chronic progressive radiation myelopathy with cavity formation in the thoracic spinal cord].

Shindo K, Nitta K, Amino A, Nagasaka T, Shiozawa Z. Shindo K, et al. Among authors: nagasaka t. Rinsho Shinkeigaku. 1995 Sep;35(9):1012-5. Rinsho Shinkeigaku. 1995. PMID: 8565337 Japanese.

7

Neuroferritinopathy in a Japanese family with a duplication in the ferritin light chain gene.

Ohta E, Nagasaka T, Shindo K, Toma S, Nagasaka K, Ohta K, Shiozawa Z. Ohta E, et al. Among authors: nagasaka k, nagasaka t. Neurology. 2008 Apr 15;70(16 Pt 2):1493-4. doi: 10.1212/01.wnl.0000310428.74624.95. Neurology. 2008. PMID: 18413574 No abstract available.

8

Clinical and histopathological features of progressive-type familial amyloidotic polyneuropathy with TTR Lys54.

Nagasaka T, Togashi S, Watanabe H, Iida H, Nagasaka K, Nakamura Y, Miwa M, Kobayashi F, Shindo K, Shiozawa Z. Nagasaka T, et al. Among authors: nagasaka k. J Neurol Sci. 2009 Jan 15;276(1-2):88-94. doi: 10.1016/j.jns.2008.09.011. Epub 2008 Oct 18. J Neurol Sci. 2009. PMID: 18930252

9

Rhythmic pupillary oscillation in Creutzfeldt-Jakob disease associated with the Glu/Lys mutation of prion protein codon 200.

Nagasaka K, Ohta E, Nagasaka T, Togashi S, Miwa M, Nakamura Y, Shindo K, Shiozawa Z. Nagasaka K, et al. Among authors: nagasaka t. Mov Disord. 2010 Jan 15;25(1):111-6. doi: 10.1002/mds.22884. Mov Disord. 2010. PMID: 20077484

10

[A case of hypokalemic myopathy induced by excessive drinking of a beverage containing green tea extract].

Fukumoto M, Yamashiro N, Kobayashi F, Nagasaka T, Takiyama Y. Fukumoto M, et al. Among authors: nagasaka t. Rinsho Shinkeigaku. 2013;53(3):239-42. doi: 10.5692/clinicalneurol.53.239. Rinsho Shinkeigaku. 2013. PMID: 23524606 Japanese.

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