Hattori N - Search Results

1

Iron Supply via NCOA4-Mediated Ferritin Degradation Maintains Mitochondrial Functions.

Fujimaki M, Furuya N, Saiki S, Amo T, Imamichi Y, Hattori N. Fujimaki M, et al. Among authors: hattori n. Mol Cell Biol. 2019 Jun 27;39(14):e00010-19. doi: 10.1128/MCB.00010-19. Print 2019 Jul 15. Mol Cell Biol. 2019. PMID: 31061094 Free PMC article.

2

Pseudo-autosomal dominant inheritance of PARK2: two families with parkin gene mutations.

Kobayashi T, Matsumine H, Zhang J, Imamichi Y, Mizuno Y, Hattori N. Kobayashi T, et al. Among authors: hattori n. J Neurol Sci. 2003 Mar 15;207(1-2):11-7. doi: 10.1016/s0022-510x(02)00358-1. J Neurol Sci. 2003. PMID: 12614925

3

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.

Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, Sato K, Hattori T, Lu CS, Inzelberg R, Djaldetti R, Melamed E, Amouri R, Gouider-Khouja N, Hentati F, Hatano Y, Wang M, Imamichi Y, Mizoguchi K, Miyajima H, Obata F, Toda T, Farrer MJ, Mizuno Y, Hattori N. Tomiyama H, et al. Among authors: hattori t, hattori n. Mov Disord. 2006 Aug;21(8):1102-8. doi: 10.1002/mds.20886. Mov Disord. 2006. PMID: 16622854

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

Neurological deficits are associated with increased brain calcinosis, hypoperfusion, and hypometabolism in idiopathic basal ganglia calcification.

Saiki M, Saiki S, Sakai K, Matsunari I, Higashi K, Murata KY, Hattori N, Hirose G. Saiki M, et al. Among authors: hattori n. Mov Disord. 2007 May 15;22(7):1027-30. doi: 10.1002/mds.21438. Mov Disord. 2007. PMID: 17357130

6

Mutation analysis of the PINK1 gene in 391 patients with Parkinson disease.

Kumazawa R, Tomiyama H, Li Y, Imamichi Y, Funayama M, Yoshino H, Yokochi F, Fukusako T, Takehisa Y, Kashihara K, Kondo T, Elibol B, Bostantjopoulou S, Toda T, Takahashi H, Yoshii F, Mizuno Y, Hattori N. Kumazawa R, et al. Among authors: hattori n. Arch Neurol. 2008 Jun;65(6):802-8. doi: 10.1001/archneur.65.6.802. Arch Neurol. 2008. PMID: 18541801

7

Familial Parkinsonism with digenic parkin and PINK1 mutations.

Funayama M, Li Y, Tsoi TH, Lam CW, Ohi T, Yazawa S, Uyama E, Djaldetti R, Melamed E, Yoshino H, Imamichi Y, Takashima H, Nishioka K, Sato K, Tomiyama H, Kubo S, Mizuno Y, Hattori N. Funayama M, et al. Among authors: hattori n. Mov Disord. 2008 Jul 30;23(10):1461-5. doi: 10.1002/mds.22143. Mov Disord. 2008. PMID: 18546294

8

Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, Japan.

Tomiyama H, Kokubo Y, Sasaki R, Li Y, Imamichi Y, Funayama M, Mizuno Y, Hattori N, Kuzuhara S. Tomiyama H, et al. Among authors: hattori n. Mov Disord. 2008 Dec 15;23(16):2344-8. doi: 10.1002/mds.22262. Mov Disord. 2008. PMID: 18759352

9

Extensive hemispheric lesions with radiological evidence of blood-brain barrier integrity in a patient with neuromyelitis optica.

Saiki S, Ueno Y, Moritani T, Sato T, Sekine T, Kawajiri S, Adachi S, Yokoyama K, Tomizawa Y, Motoi Y, Hattori N. Saiki S, et al. Among authors: hattori n. J Neurol Sci. 2009 Sep 15;284(1-2):217-9. doi: 10.1016/j.jns.2009.05.022. Epub 2009 Jun 3. J Neurol Sci. 2009. PMID: 19497587

10

[Molecular genetics and pathogenesis of Parkinson disease].

Saiki S, Hattori N. Saiki S, et al. Among authors: hattori n. No Shinkei Geka. 2009 Jun;37(6):531-41. No Shinkei Geka. 2009. PMID: 19522280 Review. Japanese. No abstract available.

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