Ueda T - Search Results

1

[A case of juvenile parkinsonism with expanded SCA8 CTA/CTG repeats].

Miyawaki T, Sekiguchi K, Yasui N, Ueda T, Kanda F, Toda T. Miyawaki T, et al. Among authors: ueda t. Rinsho Shinkeigaku. 2013;53(4):278-82. doi: 10.5692/clinicalneurol.53.278. Rinsho Shinkeigaku. 2013. PMID: 23603541 Japanese.

2

"Dropped head syndrome" caused by Lambert-Eaton myasthenic syndrome.

Ueda T, Kanda F, Kobessho H, Hamaguchi H, Motomura M. Ueda T, et al. Muscle Nerve. 2009 Jul;40(1):134-6. doi: 10.1002/mus.21301. Muscle Nerve. 2009. PMID: 19533655

3

Neuroimaging features of xeroderma pigmentosum group A.

Ueda T, Kanda F, Aoyama N, Fujii M, Nishigori C, Toda T. Ueda T, et al. Brain Behav. 2012 Jan;2(1):1-5. doi: 10.1002/brb3.22. Brain Behav. 2012. PMID: 22574268 Free PMC article.

4

A novel mutation in the C2 domain of protein kinase C gamma associated with spinocerebellar ataxia type 14.

Ueda T, Seki T, Katanazaka K, Sekiguchi K, Kobayashi K, Kanda F, Toda T. Ueda T, et al. J Neurol. 2013 Jun;260(6):1664-6. doi: 10.1007/s00415-013-6916-0. Epub 2013 Apr 21. J Neurol. 2013. PMID: 23604456 No abstract available.

5

Japanese WDR45 de novo mutation diagnosed by exome analysis: A case report.

Endo H, Uenaka T, Satake W, Suzuki Y, Tachibana H, Chihara N, Ueda T, Sekiguchi K, Mariko TI, Kowa H, Kanda F, Toda T. Endo H, et al. Among authors: ueda t. Neurol Clin Neurosci. 2017 Jul;5(4):131-133. doi: 10.1111/ncn3.12132. Epub 2017 Jun 29. Neurol Clin Neurosci. 2017. PMID: 28932395 Free PMC article.

6

Quantitative analysis of brain atrophy in patients with xeroderma pigmentosum group A carrying the founder mutation in Japan.

Ueda T, Kanda F, Nishiyama M, Nishigori C, Toda T. Ueda T, et al. J Neurol Sci. 2017 Oct 15;381:103-106. doi: 10.1016/j.jns.2017.08.3238. Epub 2017 Aug 24. J Neurol Sci. 2017. PMID: 28991657

7

Regional glucose hypometabolic spread within the primary motor cortex is associated with amyotrophic lateral sclerosis disease progression: A fluoro-deoxyglucose positron emission tomography study.

Endo H, Sekiguchi K, Ueda T, Kowa H, Kanda F, Toda T. Endo H, et al. Among authors: ueda t. eNeurologicalSci. 2017 Jan 7;6:74-79. doi: 10.1016/j.ensci.2017.01.001. eCollection 2017 Mar. eNeurologicalSci. 2017. PMID: 29260014 Free PMC article.

8

Low signal intensity in motor cortex on susceptibility-weighted MR imaging is correlated with clinical signs of amyotrophic lateral sclerosis: a pilot study.

Endo H, Sekiguchi K, Shimada H, Ueda T, Kowa H, Kanda F, Toda T. Endo H, et al. Among authors: ueda t. J Neurol. 2018 Mar;265(3):552-561. doi: 10.1007/s00415-017-8728-0. Epub 2018 Jan 22. J Neurol. 2018. PMID: 29356968

9

[Retinal vasculopathy with cerebral leukoencephalopathy carrying TREX1 mutation diagnosed by the intracranial calcification: a case report].

Komaki R, Ueda T, Tsuji Y, Miyawaki T, Kusuhara S, Hara S, Toda T. Komaki R, et al. Among authors: ueda t. Rinsho Shinkeigaku. 2018 Feb 28;58(2):111-117. doi: 10.5692/clinicalneurol.cn-001096. Epub 2018 Jan 31. Rinsho Shinkeigaku. 2018. PMID: 29386495 Japanese.

10

Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.

Higuchi Y, Okunushi R, Hara T, Hashiguchi A, Yuan J, Yoshimura A, Murayama K, Ohtake A, Ando M, Hiramatsu Y, Ishihara S, Tanabe H, Okamoto Y, Matsuura E, Ueda T, Toda T, Yamashita S, Yamada K, Koide T, Yaguchi H, Mitsui J, Ishiura H, Yoshimura J, Doi K, Morishita S, Sato K, Nakagawa M, Yamaguchi M, Tsuji S, Takashima H. Higuchi Y, et al. Among authors: ueda t. Brain. 2018 Jun 1;141(6):1622-1636. doi: 10.1093/brain/awy104. Brain. 2018. PMID: 29718187 Free PMC article.

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