Funayama M - Search Results

1

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

2

A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

Funayama M, Hasegawa K, Kowa H, Saito M, Tsuji S, Obata F. Funayama M, et al. Ann Neurol. 2002 Mar;51(3):296-301. doi: 10.1002/ana.10113. Ann Neurol. 2002. PMID: 11891824

3

Oxidative modulation of the glutathione-redox couple enhances lipopolysaccharide-induced interleukin 12 P40 production by a mouse macrophage cell line, J774A.1.

Komatsu H, Hoshino A, Funayama M, Kawahara K, Obata F. Komatsu H, et al. Among authors: funayama m. Free Radic Res. 2003 Mar;37(3):293-9. doi: 10.1080/1071576021000046613. Free Radic Res. 2003. PMID: 12688424

4

A new mutation (Thr106Ile) of the GTP cyclohydrolase 1 gene associated with DYT5 dystonia (Segawa disease).

Ohta E, Toyoshima I, Funayama M, Ichinose H, Hasegawa K, Obata F. Ohta E, et al. Among authors: funayama m. Mov Disord. 2005 Aug;20(8):1083-4. doi: 10.1002/mds.20490. Mov Disord. 2005. PMID: 15852365 No abstract available.

5

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

6

Novel mutations in the guanosine triphosphate cyclohydrolase 1 gene associated with DYT5 dystonia.

Ohta E, Funayama M, Ichinose H, Toyoshima I, Urano F, Matsuo M, Tomoko N, Yukihiko K, Yoshino S, Yokoyama H, Shimazu H, Maeda K, Hasegawa K, Obata F. Ohta E, et al. Among authors: funayama m. Arch Neurol. 2006 Nov;63(11):1605-10. doi: 10.1001/archneur.63.11.1605. Arch Neurol. 2006. PMID: 17101830

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

8

[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.

9

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

10

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.

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