Li Y - Search Results

1

Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism.

Yoshino H, Tomiyama H, Tachibana N, Ogaki K, Li Y, Funayama M, Hashimoto T, Takashima S, Hattori N. Yoshino H, et al. Among authors: li y. Neurology. 2010 Oct 12;75(15):1356-61. doi: 10.1212/WNL.0b013e3181f73649. Neurology. 2010. PMID: 20938027

2

Novel PINK1 mutations in early-onset parkinsonism.

Hatano Y, Li Y, Sato K, Asakawa S, Yamamura Y, Tomiyama H, Yoshino H, Asahina M, Kobayashi S, Hassin-Baer S, Lu CS, Ng AR, Rosales RL, Shimizu N, Toda T, Mizuno Y, Hattori N. Hatano Y, et al. Among authors: li y. Ann Neurol. 2004 Sep;56(3):424-7. doi: 10.1002/ana.20251. Ann Neurol. 2004. PMID: 15349870

3

Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism.

Li Y, Tomiyama H, Sato K, Hatano Y, Yoshino H, Atsumi M, Kitaguchi M, Sasaki S, Kawaguchi S, Miyajima H, Toda T, Mizuno Y, Hattori N. Li Y, et al. Neurology. 2005 Jun 14;64(11):1955-7. doi: 10.1212/01.WNL.0000164009.36740.4E. Neurology. 2005. PMID: 15955953

4

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: li y. Mov Disord. 2006 Aug;21(8):1102-8. doi: 10.1002/mds.20886. Mov Disord. 2006. PMID: 16622854

5

[A 62-year-old woman with early-onset Parkinson's disease associated with the PINKi gene deletion].

Atsumi M, Li Y, Tomiyama H, Sato K, Hattori N. Atsumi M, et al. Among authors: li y. Rinsho Shinkeigaku. 2006 Mar;46(3):199-202. Rinsho Shinkeigaku. 2006. PMID: 16642930 Japanese.

6

Progress in familial Parkinson's disease.

Mizuno Y, Hattori N, Yoshino H, Hatano Y, Satoh K, Tomiyama H, Li Y. Mizuno Y, et al. Among authors: li y. J Neural Transm Suppl. 2006;(70):191-204. doi: 10.1007/978-3-211-45295-0_30. J Neural Transm Suppl. 2006. PMID: 17017529 Review.

7

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: li y. Neuroreport. 2007 Feb 12;18(3):273-5. doi: 10.1097/WNR.0b013e32801254b6. Neuroreport. 2007. PMID: 17314670

8

PARK9-linked parkinsonism in eastern Asia: mutation detection in ATP13A2 and clinical phenotype.

Ning YP, Kanai K, Tomiyama H, Li Y, Funayama M, Yoshino H, Sato S, Asahina M, Kuwabara S, Takeda A, Hattori T, Mizuno Y, Hattori N. Ning YP, et al. Among authors: li y. Neurology. 2008 Apr 15;70(16 Pt 2):1491-3. doi: 10.1212/01.wnl.0000310427.72236.68. Neurology. 2008. PMID: 18413573 No abstract available.

9

Screening PARK genes for mutations in early-onset Parkinson's disease patients from Queensland, Australia.

Mellick GD, Siebert GA, Funayama M, Buchanan DD, Li Y, Imamichi Y, Yoshino H, Silburn PA, Hattori N. Mellick GD, et al. Among authors: li y. Parkinsonism Relat Disord. 2009 Feb;15(2):105-9. doi: 10.1016/j.parkreldis.2007.11.016. Epub 2008 May 19. Parkinsonism Relat Disord. 2009. PMID: 18486522 Free article.

10

A new mutation in the GCH1 gene presents as early-onset Parkinsonism.

Momma K, Funayama M, Li Y, Ichinose H, Motoyoshi K, Hattori N, Mizuno Y, Kamakura K. Momma K, et al. Among authors: li y. Parkinsonism Relat Disord. 2009 Feb;15(2):160-1. doi: 10.1016/j.parkreldis.2007.12.010. Epub 2008 Jun 3. Parkinsonism Relat Disord. 2009. PMID: 18511327 No abstract available.

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