Yasuda T - Search Results

1

Clinical and imaging findings of progressive supranuclear palsy with predominant cerebellar ataxia.

Shimohata T, Kanazawa M, Yoshida M, Saito Y, Iwai K, Yasuda T, Inukai A, Takahashi H, Nishizawa M, Aiba I. Shimohata T, et al. Among authors: yasuda t. Mov Disord. 2016 May;31(5):760-2. doi: 10.1002/mds.26618. Epub 2016 Mar 31. Mov Disord. 2016. PMID: 27030358 No abstract available.

2

Longitudinal MRI study of multiple system atrophy - when do the findings appear, and what is the course?

Horimoto Y, Aiba I, Yasuda T, Ohkawa Y, Katayama T, Yokokawa Y, Goto A, Ito Y. Horimoto Y, et al. Among authors: yasuda t. J Neurol. 2002 Jul;249(7):847-54. doi: 10.1007/s00415-002-0734-0. J Neurol. 2002. PMID: 12140668

3

Neuroradiologic and clinical abnormalities in dementia of diffuse neurofibrillary tangles with calcification (Kosaka-Shibayama disease).

Ito Y, Kato T, Suzuki T, Yokokawa Y, Aiba I, Arahata Y, Ito E, Ito K, Yasuda T, Sobue G. Ito Y, et al. Among authors: yasuda t. J Neurol Sci. 2003 May 15;209(1-2):105-9. doi: 10.1016/s0022-510x(02)00468-9. J Neurol Sci. 2003. PMID: 12686411

4

[A case of amyloid-β-related cerebral angiitis with ApoE ε4/ε2 genotype].

Ogura A, Moriyoshi H, Nakai N, Nishida S, Kitagawa S, Yoshida M, Yasuda T, Ito Y. Ogura A, et al. Among authors: yasuda t. Rinsho Shinkeigaku. 2015;55(8):561-6. doi: 10.5692/clinicalneurol.cn-000685. Epub 2015 Jun 18. Rinsho Shinkeigaku. 2015. PMID: 26084230 Japanese.

5

Systemic angiopathy and axonopathy in hereditary transthyretin amyloidosis with Ala97Gly (p. Ala117Gly) mutation: a post-mortem analysis.

Koike H, Yasuda T, Nishi R, Ikeda S, Kawagashira Y, Iijima M, Sobue G, Katsuno M. Koike H, et al. Among authors: yasuda t. Amyloid. 2018 Jun;25(2):141-142. doi: 10.1080/13506129.2018.1474734. Epub 2018 Jun 1. Amyloid. 2018. PMID: 29855203 No abstract available.

6

Gastro-intestinal Involvement in m.3243A>G-associated Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.

Suzuki J, Iwata M, Moriyoshi H, Nishida S, Yasuda T, Ito Y. Suzuki J, et al. Among authors: yasuda t. Intern Med. 2018 Mar 1;57(5):771. doi: 10.2169/internalmedicine.9632-17. Epub 2017 Nov 20. Intern Med. 2018. PMID: 29151541 Free PMC article. No abstract available.

7

Familial Pernicious Chronic Intestinal Pseudo-obstruction with a Mitochondrial DNA A3243G Mutation.

Suzuki J, Iwata M, Moriyoshi H, Nishida S, Yasuda T, Ito Y. Suzuki J, et al. Among authors: yasuda t. Intern Med. 2017;56(9):1089-1093. doi: 10.2169/internalmedicine.56.7753. Epub 2017 May 1. Intern Med. 2017. PMID: 28458318 Free PMC article.

8

Common clinicopathological features in late-onset hereditary transthyretin amyloidosis (Ala97Gly, Val94Gly and Val30Met).

Koike H, Nakamura T, Nishi R, Ikeda S, Kawagashira Y, Iijima M, Yasuda T, Mukai E, Date Y, Shiomi K, Nakazato M, Katsuno M, Sobue G. Koike H, et al. Among authors: yasuda t. Amyloid. 2019;26(sup1):24-25. doi: 10.1080/13506129.2019.1582495. Amyloid. 2019. PMID: 31343348 No abstract available.

9

[Reversible cerebral vasoconstriction syndrome with cortical subarachnoid hemorrhage presenting as thunderclap headache-a long followed up case].

Ogura A, Suzuki J, Imai K, Nishida S, Kato T, Yasuda T, Ito Y. Ogura A, et al. Among authors: yasuda t. Rinsho Shinkeigaku. 2013;53(8):618-23. doi: 10.5692/clinicalneurol.53.618. Rinsho Shinkeigaku. 2013. PMID: 23965853 Japanese.

10

[A Japanese SUNA patient with migraine without aura and medication overuse headache responsive to topiramate].

Ito Y, Hakusui S, Ogura A, Imai K, Nishida S, Yasuda T. Ito Y, et al. Among authors: yasuda t. Rinsho Shinkeigaku. 2013;53(9):728-31. doi: 10.5692/clinicalneurol.53.728. Rinsho Shinkeigaku. 2013. PMID: 24097323 Japanese.

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