Hashimoto T - Search Results

1

Oyanagi K, Yamada M, Hineno A, Yahikozawa H, Ushiyama M, Miki J, Kanno H, Nakayama J, Makishita H, Inoue K, Ohara S, Hayashida K, Kayanuma K, Yamamoto K, Yasude T, Hashimoto T, Yoshida K, Ikeda SI. Oyanagi K, et al. Among authors: hashimoto t. Neuropathology. 2016 Dec;36(6):600-601. doi: 10.1111/neup.12304. Epub 2016 May 5. Neuropathology. 2016. PMID: 27147541 No abstract available.

2

Axonal TDP-43 aggregates in sporadic amyotrophic lateral sclerosis.

Onozato T, Nakahara A, Suzuki-Kouyama E, Hineno A, Yasude T, Nakamura T, Yahikozawa H, Watanabe M, Kayanuma K, Makishita H, Ohara S, Hashimoto T, Higuchi K, Sakai T, Asano K, Hashimoto T, Kanno H, Nakayama J, Oyanagi K. Onozato T, et al. Among authors: hashimoto t. Neuropathol Appl Neurobiol. 2016 Oct;42(6):561-72. doi: 10.1111/nan.12310. Epub 2016 Mar 22. Neuropathol Appl Neurobiol. 2016. PMID: 26819002

3

Chronic inflammatory demyelinating polyradiculoneuropathy with autonomic involvement.

Yamamoto K, Watarai M, Hashimoto T, Ikeda S. Yamamoto K, et al. Among authors: hashimoto t. Muscle Nerve. 2005 Jan;31(1):108-12. doi: 10.1002/mus.20140. Muscle Nerve. 2005. PMID: 15389651

4

Hereditary diffuse leukoencephalopathy with axonal spheroids caused by R782H mutation in CSF1R: case report.

Kinoshita M, Yoshida K, Oyanagi K, Hashimoto T, Ikeda S. Kinoshita M, et al. Among authors: hashimoto t. J Neurol Sci. 2012 Jul 15;318(1-2):115-8. doi: 10.1016/j.jns.2012.03.012. Epub 2012 Apr 14. J Neurol Sci. 2012. PMID: 22503135

5

Static balance impairment and its change after pallidotomy in Parkinson's disease.

Hagiwara N, Hashimoto T, Ikeda S. Hagiwara N, et al. Among authors: hashimoto t. Mov Disord. 2004 Apr;19(4):437-45. doi: 10.1002/mds.10666. Mov Disord. 2004. PMID: 15077242

6

Regional features of autosomal-dominant cerebellar ataxia in Nagano: clinical and molecular genetic analysis of 86 families.

Shimizu Y, Yoshida K, Okano T, Ohara S, Hashimoto T, Fukushima Y, Ikeda SI. Shimizu Y, et al. Among authors: hashimoto t. J Hum Genet. 2004;49(11):610-616. doi: 10.1007/s10038-004-0196-6. Epub 2004 Oct 8. J Hum Genet. 2004. PMID: 15480876

7

Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation.

Tojo K, Sekijima Y, Suzuki T, Suzuki N, Tomita Y, Yoshida K, Hashimoto T, Ikeda S. Tojo K, et al. Among authors: hashimoto t. Mov Disord. 2006 Sep;21(9):1510-3. doi: 10.1002/mds.21011. Mov Disord. 2006. PMID: 16817193

8

Klüver-Bucy syndrome following status epilepticus associated with hepatic encephalopathy.

Naito K, Hashimoto T, Ikeda S. Naito K, et al. Among authors: hashimoto t. Epilepsy Behav. 2008 Feb;12(2):337-9. doi: 10.1016/j.yebeh.2007.09.017. Epub 2007 Nov 5. Epilepsy Behav. 2008. PMID: 17980671

9

EEG-EMG polygraphic study of dystonia and myoclonus in a case of Creutzfeldt-Jakob disease.

Hashimoto T, Iwahashi T, Ishii W, Yamamoto K, Ikeda S. Hashimoto T, et al. Epilepsy Behav Case Rep. 2015 Jun 20;4:30-2. doi: 10.1016/j.ebcr.2015.05.002. eCollection 2015. Epilepsy Behav Case Rep. 2015. PMID: 26150924 Free PMC article.

10

[Two patients with different types of vasculitic neuropathy--a comparison between cutaneous polyarteritis nodosa and nonsystemic vasculitic neuropathy].

Hagiwara N, Sekijima Y, Hattori T, Hashimoto T, Ikeda S. Hagiwara N, et al. Among authors: hashimoto t. Rinsho Shinkeigaku. 2003 Mar;43(3):102-8. Rinsho Shinkeigaku. 2003. PMID: 12820558 Japanese.

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