Hattori N - Search Results

1

Erratum to: A randomized double-blind multi-center trial of hydrogen water for Parkinson's disease: protocol and baseline characteristics.

Yoritaka A, Abe T, Ohtsuka C, Maeda T, Hirayama M, Watanabe H, Saiki H, Oyama G, Fukae J, Shimo Y, Hatano T, Kawajiri S, Okuma Y, Machida Y, Miwa H, Suzuki C, Kazama A, Tomiyama M, Kihara T, Hirasawa M, Shimura H, Hattori N. Yoritaka A, et al. Among authors: hattori n. BMC Neurol. 2017 Feb 20;17(1):35. doi: 10.1186/s12883-017-0817-2. BMC Neurol. 2017. PMID: 28219346 Free PMC article. No abstract available.

2

MRI findings in the mild type of mucopolysaccharidosis II (Hunter's syndrome).

Shimoda-Matsubayashi S, Kuru Y, Sumie H, Ito T, Hattori N, Okuma Y, Mizuno Y. Shimoda-Matsubayashi S, et al. Among authors: hattori n. Neuroradiology. 1990;32(4):328-30. doi: 10.1007/BF00593056. Neuroradiology. 1990. PMID: 2122274

3

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.

4

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

5

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.

6

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

7

[A 74-year-old woman with parkinsonism and dementia who died four years after the onset].

Okuma Y, Hattori N, Nobukawa B, Mori H, Suda K, Takubo H, Mizuno Y. Okuma Y, et al. Among authors: hattori n. No To Shinkei. 1998 Jul;50(7):671-82. No To Shinkei. 1998. PMID: 9739528 Japanese.

8

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

9

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

10

Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients.

Shimura H, Hattori N, Kubo S, Yoshikawa M, Kitada T, Matsumine H, Asakawa S, Minoshima S, Yamamura Y, Shimizu N, Mizuno Y. Shimura H, et al. Among authors: hattori n. Ann Neurol. 1999 May;45(5):668-72. doi: 10.1002/1531-8249(199905)45:5<668::aid-ana19>3.0.co;2-z. Ann Neurol. 1999. PMID: 10319893

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