Takeda A - Search Results

1

PARK9-linked parkinsonism in eastern Asia: mutation detection in ATP13A2 and clinical phenotype.

Ning YP, Kanai K, Tomiyama H, Li Y, Funayama M, Yoshino H, Sato S, Asahina M, Kuwabara S, Takeda A, Hattori T, Mizuno Y, Hattori N. Ning YP, et al. Among authors: takeda a. Neurology. 2008 Apr 15;70(16 Pt 2):1491-3. doi: 10.1212/01.wnl.0000310427.72236.68. Neurology. 2008. PMID: 18413573 No abstract available.

2

CSF tau protein: a new prognostic marker for Guillain-Barré syndrome.

Jin K, Takeda A, Shiga Y, Sato S, Ohnuma A, Nomura H, Arai H, Kusunoki S, Ikeda M, Itoyama Y. Jin K, et al. Among authors: takeda a. Neurology. 2006 Oct 24;67(8):1470-2. doi: 10.1212/01.wnl.0000240119.29939.c7. Neurology. 2006. PMID: 17060576

3

Familial neuromyelitis optica (Devic's syndrome) with late onset in Japan.

Yamakawa K, Kuroda H, Fujihara K, Sato S, Nakashima I, Takeda A, Suzuki K, Itoyama Y. Yamakawa K, et al. Among authors: takeda a. Neurology. 2000 Jul 25;55(2):318-20. doi: 10.1212/wnl.55.2.318. Neurology. 2000. PMID: 10908921 No abstract available.

4

Cognitive impairments in multiple system atrophy: MSA-C vs MSA-P.

Kawai Y, Suenaga M, Takeda A, Ito M, Watanabe H, Tanaka F, Kato K, Fukatsu H, Naganawa S, Kato T, Ito K, Sobue G. Kawai Y, et al. Among authors: takeda a. Neurology. 2008 Apr 15;70(16 Pt 2):1390-6. doi: 10.1212/01.wnl.0000310413.04462.6a. Neurology. 2008. PMID: 18413566

5

Induction of midkine expression in reactive astrocytes following rat transient forebrain ischemia.

Mochizuki R, Takeda A, Sato N, Kimpara T, Onodera H, Itoyama Y, Muramatsu T. Mochizuki R, et al. Among authors: takeda a. Exp Neurol. 1998 Jan;149(1):73-8. doi: 10.1006/exnr.1997.6687. Exp Neurol. 1998. PMID: 9454616

6

Upregulation of Bcl-2 protein in the myasthenic thymus.

Onodera J, Nakamura S, Nagano I, tobita M, Yoshioka M, Takeda A, Oouchi M, Itoyama Y. Onodera J, et al. Among authors: takeda a. Ann Neurol. 1996 Apr;39(4):521-8. doi: 10.1002/ana.410390414. Ann Neurol. 1996. PMID: 8619530

7

Cardiac (123)I-meta-iodobenzylguanidine (MIBG) uptake in dementia with Lewy bodies: comparison with Alzheimer's disease.

Watanabe H, Ieda T, Katayama T, Takeda A, Aiba I, Doyu M, Hirayama M, Sobue G. Watanabe H, et al. Among authors: takeda a. J Neurol Neurosurg Psychiatry. 2001 Jun;70(6):781-3. doi: 10.1136/jnnp.70.6.781. J Neurol Neurosurg Psychiatry. 2001. PMID: 11385013 Free PMC article.

8

Mutation in the alpha-synuclein gene and sporadic Parkinson's disease, Alzheimer's disease, and dementia with lewy bodies.

Higuchi S, Arai H, Matsushita S, Matsui T, Kimpara T, Takeda A, Shirakura K. Higuchi S, et al. Among authors: takeda a. Exp Neurol. 1998 Sep;153(1):164-6. doi: 10.1006/exnr.1998.6868. Exp Neurol. 1998. PMID: 9743579

9

Corticolimbic gray matter loss in Parkinson's disease without dementia.

Nishio Y, Hirayama K, Takeda A, Hosokai Y, Ishioka T, Suzuki K, Itoyama Y, Takahashi S, Mori E. Nishio Y, et al. Among authors: takeda a. Eur J Neurol. 2010 Aug;17(8):1090-7. doi: 10.1111/j.1468-1331.2010.02980.x. Epub 2010 Mar 9. Eur J Neurol. 2010. PMID: 20298422

10

[Progressive cerebellar ataxia and distal amyotrophy of Charcot-Marie-Tooth type with hyperglutamataemia:two sibling cases].

Tanji H, Takeda A, Tateyama M, Mochizuki H, Itoyama Y. Tanji H, et al. Among authors: takeda a. Rinsho Shinkeigaku. 1995 Jul;35(7):793-7. Rinsho Shinkeigaku. 1995. PMID: 8777805 Japanese.

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