Funayama M - Search Results

1

Preserved cardiac (123)I-MIBG uptake and lack of severe autonomic dysfunction in a PARK9 patient.

Kanai K, Asahina M, Arai K, Tomiyama H, Kuwabara Y, Uchiyama T, Sekiguchi Y, Funayama M, Kuwabara S, Hattori N, Hattori T. Kanai K, et al. Among authors: funayama m. Mov Disord. 2009 Jul 15;24(9):1403-4. doi: 10.1002/mds.22520. Mov Disord. 2009. PMID: 19412962 No abstract available.

2

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

3

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

4

[Molecular genetics of PINK1].

Funayama M, Hattori N. Funayama M, et al. Brain Nerve. 2007 Aug;59(8):831-8. Brain Nerve. 2007. PMID: 17713119 Review. Japanese.

5

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: funayama m. 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.

6

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: funayama m. 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.

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. 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: funayama m. Mov Disord. 2008 Dec 15;23(16):2344-8. doi: 10.1002/mds.22262. Mov Disord. 2008. PMID: 18759352

9

No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients.

Li L, Funayama M, Tomiyama H, Li Y, Yoshino H, Sasaki R, Kokubo Y, Kuzuhara S, Mizuno Y, Hattori N. Li L, et al. Among authors: funayama m. Neurosci Lett. 2010 Aug 2;479(3):245-8. doi: 10.1016/j.neulet.2010.05.071. Neurosci Lett. 2010. PMID: 20641165

10

Clinical course of the first Asian family with Parkinsonism related to SNCA triplication.

Sekine T, Kagaya H, Funayama M, Li Y, Yoshino H, Tomiyama H, Hattori N. Sekine T, et al. Among authors: funayama m. Mov Disord. 2010 Dec 15;25(16):2871-5. doi: 10.1002/mds.23313. Mov Disord. 2010. PMID: 20818659

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