Ohnari K - Search Results

1

Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patients.

Yoshida T, Sasayama H, Mizuta I, Okamoto Y, Yoshida M, Riku Y, Hayashi Y, Yonezu T, Takata Y, Ohnari K, Okuda S, Aiba I, Nakagawa M. Yoshida T, et al. Among authors: ohnari k. Acta Neurol Scand. 2011 Aug;124(2):104-8. doi: 10.1111/j.1600-0404.2010.01427.x. Epub 2010 Sep 16. Acta Neurol Scand. 2011. PMID: 20849398

2

An adult form of Alexander disease: a novel mutation in glial fibrillary acidic protein.

Ohnari K, Yamano M, Uozumi T, Hashimoto T, Tsuji S, Nakagawa M. Ohnari K, et al. J Neurol. 2007 Oct;254(10):1390-4. doi: 10.1007/s00415-007-0557-0. Epub 2007 Oct 15. J Neurol. 2007. PMID: 17934883

3

Effects of a polymorphism in the GFAP promoter on the age of onset and ambulatory disability in late-onset Alexander disease.

Yoshida T, Mizuta I, Saito K, Ohara R, Kurisaki H, Ohnari K, Riku Y, Hayashi Y, Suzuki H, Shii H, Fujiwara Y, Yonezu T, Nagaishi A, Nakagawa M. Yoshida T, et al. Among authors: ohnari k. J Hum Genet. 2013 Sep;58(9):635-8. doi: 10.1038/jhg.2013.83. Epub 2013 Aug 1. J Hum Genet. 2013. PMID: 23903069

4

Severe symptoms of 16q-ADCA coexisting with SCA8 repeat expansion.

Ohnari K, Aoki M, Uozumi T, Tsuji S. Ohnari K, et al. J Neurol Sci. 2008 Oct 15;273(1-2):15-8. doi: 10.1016/j.jns.2008.06.003. Epub 2008 Aug 6. J Neurol Sci. 2008. PMID: 18684474

5

[A family of hereditary motor and sensory neuropathy type I with a new type of myelin P0 mutation].

Ohnishi A, Ohnari K, Hashimoto T, Hayasaka K, Yoshimura T, Fukushima Y. Ohnishi A, et al. Among authors: ohnari k. Rinsho Shinkeigaku. 1994 Jun;34(6):546-51. Rinsho Shinkeigaku. 1994. PMID: 7525134 Japanese.

6

[A case of acute polyradiculoneuropathy with autonomic disturbances following rubella infection].

Ohnari K, Ohnishi A, Hashimoto T, Yamamoto T, Tsuji S, Murai Y. Ohnari K, et al. J UOEH. 1993 Dec 1;15(4):297-302. doi: 10.7888/juoeh.15.297. J UOEH. 1993. PMID: 8265890 Review. Japanese.

7

Unilateral positive-negative myoclonus in Creutzfeldt-Jakob disease.

Ohnari K, Matsunaga K, Uozumi T, Tamagawa A, Hashimoto T, Tsuji S. Ohnari K, et al. Mov Disord. 2006 Nov;21(11):1963-6. doi: 10.1002/mds.21078. Mov Disord. 2006. PMID: 16960864

8

[Occupation and carpal tunnel syndrome].

Ohnari K, Uozumi T, Tsuji S. Ohnari K, et al. Brain Nerve. 2007 Nov;59(11):1247-52. Brain Nerve. 2007. PMID: 18044201 Review. Japanese.

9

Levels of nitric oxide metabolites in cerebrospinal fluid correlate with cognitive impairment in early stage multiple sclerosis.

Okada K, Kobata M, Sennari Y, Iwanaka Y, Hashimoto T, Ohnari K, Tahara M. Okada K, et al. Among authors: ohnari k. J Neurol Neurosurg Psychiatry. 2017 Oct;88(10):892-893. doi: 10.1136/jnnp-2017-315585. Epub 2017 Apr 26. J Neurol Neurosurg Psychiatry. 2017. PMID: 28446603 No abstract available.

10

[Idiopathic acquired generalized anhidrosis with normal numbers of eccrine gland nerve terminals and unmyelinated axons. A case report].

Muta Y, Ohnishi A, Ohnari K, Oishi T, Murai Y. Muta Y, et al. Among authors: ohnari k. Rinsho Shinkeigaku. 1995 Jun;35(6):638-42. Rinsho Shinkeigaku. 1995. PMID: 8521640 Japanese.

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