Hattori N - Search Results

1

Cerebral infarction in a young man using high-dose anabolic steroids.

Shimada Y, Yoritaka A, Tanaka Y, Miyamoto N, Ueno Y, Hattori N, Takao U. Shimada Y, et al. Among authors: hattori n. J Stroke Cerebrovasc Dis. 2012 Nov;21(8):906.e9-11. doi: 10.1016/j.jstrokecerebrovasdis.2011.07.013. Epub 2011 Sep 8. J Stroke Cerebrovasc Dis. 2012. PMID: 21903417

2

Immunohistochemical detection of 4-hydroxynonenal protein adducts in Parkinson disease.

Yoritaka A, Hattori N, Uchida K, Tanaka M, Stadtman ER, Mizuno Y. Yoritaka A, et al. Among authors: hattori n. Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):2696-701. doi: 10.1073/pnas.93.7.2696. Proc Natl Acad Sci U S A. 1996. PMID: 8610103 Free PMC article.

3

An immunohistochemical study on manganese superoxide dismutase in Parkinson's disease.

Yoritaka A, Hattori N, Mori H, Kato K, Mizuno Y. Yoritaka A, et al. Among authors: hattori n. J Neurol Sci. 1997 May 29;148(2):181-6. doi: 10.1016/s0022-510x(96)05339-7. J Neurol Sci. 1997. PMID: 9129114

4

Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan. Short communication.

Yoritaka A, Hattori N, Yoshino H, Mizuno Y. Yoritaka A, et al. Among authors: hattori n. J Neural Transm (Vienna). 1997;104(11-12):1313-7. doi: 10.1007/BF01294732. J Neural Transm (Vienna). 1997. PMID: 9503277 Clinical Trial.

5

A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2).

Matsumine H, Yamamura Y, Hattori N, Kobayashi T, Kitada T, Yoritaka A, Mizuno Y. Matsumine H, et al. Among authors: hattori n. Genomics. 1998 Apr 1;49(1):143-6. doi: 10.1006/geno.1997.5196. Genomics. 1998. PMID: 9570960

6

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

Hattori N, Matsumine H, Asakawa S, Kitada T, Yoshino H, Elibol B, Brookes AJ, Yamamura Y, Kobayashi T, Wang M, Yoritaka A, Minoshima S, Shimizu N, Mizuno Y. Hattori N, et al. Biochem Biophys Res Commun. 1998 Aug 28;249(3):754-8. doi: 10.1006/bbrc.1998.9134. Biochem Biophys Res Commun. 1998. PMID: 9731209

7

Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.

Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kobayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y. Hattori N, et al. Ann Neurol. 1998 Dec;44(6):935-41. doi: 10.1002/ana.410440612. Ann Neurol. 1998. PMID: 9851438

8

A large Japanese family with Machado-Joseph disease: clinical and genetic analysis.

Yoritaka A, Nakagawa-Hattori Y, Hattori N, Kitahara A, Mizuno Y. Yoritaka A, et al. Among authors: hattori n. Acta Neurol Scand. 1999 Apr;99(4):241-4. doi: 10.1111/j.1600-0404.1999.tb07354.x. Acta Neurol Scand. 1999. PMID: 10225355

9

Polymorphism of the lipoprotein lipase gene and risk of atherothrombotic cerebral infarction in the Japanese.

Shimo-Nakanishi Y, Urabe T, Hattori N, Watanabe Y, Nagao T, Yokochi M, Hamamoto M, Mizuno Y. Shimo-Nakanishi Y, et al. Among authors: hattori n. Stroke. 2001 Jul;32(7):1481-6. doi: 10.1161/01.str.32.7.1481. Stroke. 2001. PMID: 11441189

10

Mobile aortic plaques are a cause of multiple brain infarcts seen on diffusion-weighted imaging.

Ueno Y, Kimura K, Iguchi Y, Shibazaki K, Inoue T, Hattori N, Urabe T. Ueno Y, et al. Among authors: hattori n. Stroke. 2007 Sep;38(9):2470-6. doi: 10.1161/STROKEAHA.107.482497. Epub 2007 Aug 2. Stroke. 2007. PMID: 17673730

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