Funayama M - 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: funayama m. Neurology. 2010 Oct 12;75(15):1356-61. doi: 10.1212/WNL.0b013e3181f73649. Neurology. 2010. PMID: 20938027

2

Catecholaminergic neurons in the diencephalon and basal ganglia of SIDS.

Ozawa Y, Obonai T, Itoh M, Aoki Y, Funayama M, Takashima S. Ozawa Y, et al. Among authors: funayama m. Pediatr Neurol. 1999 Jul;21(1):471-5. doi: 10.1016/s0887-8994(99)00033-8. Pediatr Neurol. 1999. PMID: 10428433

3

An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.

Funayama M, Hasegawa K, Ohta E, Kawashima N, Komiyama M, Kowa H, Tsuji S, Obata F. Funayama M, et al. Ann Neurol. 2005 Jun;57(6):918-21. doi: 10.1002/ana.20484. Ann Neurol. 2005. PMID: 15880653

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

5

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

6

[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.

7

Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease.

Ross OA, Wu YR, Lee MC, Funayama M, Chen ML, Soto AI, Mata IF, Lee-Chen GJ, Chen CM, Tang M, Zhao Y, Hattori N, Farrer MJ, Tan EK, Wu RM. Ross OA, et al. Among authors: funayama m. Ann Neurol. 2008 Jul;64(1):88-92. doi: 10.1002/ana.21405. Ann Neurol. 2008. PMID: 18412265

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: 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.

9

Progress in the pathogenesis and genetics of Parkinson's disease.

Mizuno Y, Hattori N, Kubo S, Sato S, Nishioka K, Hatano T, Tomiyama H, Funayama M, Machida Y, Mochizuki H. Mizuno Y, et al. Among authors: funayama m. Philos Trans R Soc Lond B Biol Sci. 2008 Jun 27;363(1500):2215-27. doi: 10.1098/rstb.2008.2273. Philos Trans R Soc Lond B Biol Sci. 2008. PMID: 18426756 Free PMC article. Review.

10

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: funayama m. 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.

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