Hattori N - Search Results

1

Reduced astrocytic reactivity in human brains and midbrain organoids with PRKN mutations.

Kano M, Takanashi M, Oyama G, Yoritaka A, Hatano T, Shiba-Fukushima K, Nagai M, Nishiyama K, Hasegawa K, Inoshita T, Ishikawa KI, Akamatsu W, Imai Y, Bolognin S, Schwamborn JC, Hattori N. Kano M, et al. Among authors: hattori n. NPJ Parkinsons Dis. 2020 Nov 13;6(1):33. doi: 10.1038/s41531-020-00137-8. NPJ Parkinsons Dis. 2020. PMID: 33298969 Free PMC article.

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

[An 80-year-old woman with parkinsonism and progressive dementia].

Hattori N, Sumino S, Takanashi M, Mori H, Wakiya M, Shirai T, Sugita H, Mizuno Y. Hattori N, et al. No To Shinkei. 1999 Jun;51(6):541-50. No To Shinkei. 1999. PMID: 10423759 Japanese.

10

[A 57-year-old woman with progressive disturbance of gait and mental deterioration].

Kubo S, Hattori T, Takanashi M, Mori H, Mizutani Y, Suda K, Hattori N, Mizuno Y. Kubo S, et al. Among authors: hattori t, hattori n. No To Shinkei. 2000 Nov;52(11):1035-44. No To Shinkei. 2000. PMID: 11217688 Japanese.

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