Hattori N - Search Results

1

Plasmablasts as migratory IgG-producing cells in the pathogenesis of neuromyelitis optica.

Chihara N, Aranami T, Oki S, Matsuoka T, Nakamura M, Kishida H, Yokoyama K, Kuroiwa Y, Hattori N, Okamoto T, Murata M, Toda T, Miyake S, Yamamura T. Chihara N, et al. Among authors: hattori n. PLoS One. 2013 Dec 10;8(12):e83036. doi: 10.1371/journal.pone.0083036. eCollection 2013. PLoS One. 2013. PMID: 24340077 Free PMC article.

2

Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease.

Nishioka K, Hayashi S, Farrer MJ, Singleton AB, Yoshino H, Imai H, Kitami T, Sato K, Kuroda R, Tomiyama H, Mizoguchi K, Murata M, Toda T, Imoto I, Inazawa J, Mizuno Y, Hattori N. Nishioka K, et al. Among authors: hattori n. Ann Neurol. 2006 Feb;59(2):298-309. doi: 10.1002/ana.20753. Ann Neurol. 2006. PMID: 16358335

3

Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.

Mizuta I, Satake W, Nakabayashi Y, Ito C, Suzuki S, Momose Y, Nagai Y, Oka A, Inoko H, Fukae J, Saito Y, Sawabe M, Murayama S, Yamamoto M, Hattori N, Murata M, Toda T. Mizuta I, et al. Among authors: hattori n. Hum Mol Genet. 2006 Apr 1;15(7):1151-8. doi: 10.1093/hmg/ddl030. Epub 2006 Feb 24. Hum Mol Genet. 2006. PMID: 16500997

4

Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population.

Funayama M, Li Y, Tomiyama H, Yoshino H, Imamichi Y, Yamamoto M, Murata M, Toda T, Mizuno Y, Hattori N. Funayama M, et al. Among authors: hattori n. Neuroreport. 2007 Feb 12;18(3):273-5. doi: 10.1097/WNR.0b013e32801254b6. Neuroreport. 2007. PMID: 17314670

5

Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.

Satake W, Mizuta I, Suzuki S, Nakabayashi Y, Ito C, Watanabe M, Takeda A, Hasegawa K, Sakoda S, Yamamoto M, Hattori N, Murata M, Toda T. Satake W, et al. Among authors: hattori n. Neuroreport. 2007 Jun 11;18(9):937-40. doi: 10.1097/WNR.0b013e328133265b. Neuroreport. 2007. PMID: 17515805

6

Calbindin 1, fibroblast growth factor 20, and alpha-synuclein in sporadic Parkinson's disease.

Mizuta I, Tsunoda T, Satake W, Nakabayashi Y, Watanabe M, Takeda A, Hasegawa K, Nakashima K, Yamamoto M, Hattori N, Murata M, Toda T. Mizuta I, et al. Among authors: hattori n. Hum Genet. 2008 Aug;124(1):89-94. doi: 10.1007/s00439-008-0525-5. Epub 2008 Jun 22. Hum Genet. 2008. PMID: 18568448

7

LRRK2 P755L variant in sporadic Parkinson's disease.

Tomiyama H, Mizuta I, Li Y, Funayama M, Yoshino H, Li L, Murata M, Yamamoto M, Kubo SI, Mizuno Y, Toda T, Hattori N. Tomiyama H, et al. Among authors: hattori n. J Hum Genet. 2008;53(11-12):1012-1015. doi: 10.1007/s10038-008-0336-5. Epub 2008 Oct 16. J Hum Genet. 2008. PMID: 18923807

8

Linear medullary pericanal lesion with longitudinal myelitis can be diagnostic of neuromyelitis optica.

Tomizawa Y, Fukae J, Noda K, Fujishima K, Yokoyama K, Hattori N, Takahashi T, Okuma Y. Tomizawa Y, et al. Among authors: hattori n. Intern Med. 2009;48(3):175-6. doi: 10.2169/internalmedicine.48.1719. Epub 2009 Feb 2. Intern Med. 2009. PMID: 19182430 Free article. No abstract available.

9

Mutation analysis for DJ-1 in sporadic and familial parkinsonism: screening strategy in parkinsonism.

Tomiyama H, Li Y, Yoshino H, Mizuno Y, Kubo S, Toda T, Hattori N. Tomiyama H, et al. Among authors: hattori n. Neurosci Lett. 2009 May 22;455(3):159-61. doi: 10.1016/j.neulet.2009.03.033. Epub 2009 Mar 16. Neurosci Lett. 2009. PMID: 19429112

10

Mutations for Gaucher disease confer high susceptibility to Parkinson disease.

Mitsui J, Mizuta I, Toyoda A, Ashida R, Takahashi Y, Goto J, Fukuda Y, Date H, Iwata A, Yamamoto M, Hattori N, Murata M, Toda T, Tsuji S. Mitsui J, et al. Among authors: hattori n. Arch Neurol. 2009 May;66(5):571-6. doi: 10.1001/archneurol.2009.72. Arch Neurol. 2009. PMID: 19433656

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