Chen CM - Search Results

1

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: chen ml, chen cm. Ann Neurol. 2008 Jul;64(1):88-92. doi: 10.1002/ana.21405. Ann Neurol. 2008. PMID: 18412265

2

Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson's disease.

Wu YR, Wang CK, Chen CM, Hsu Y, Lin SJ, Lin YY, Fung HC, Chang KH, Lee-Chen GJ. Wu YR, et al. Among authors: chen cm. Hum Genet. 2004 Feb;114(3):236-41. doi: 10.1007/s00439-003-1050-1. Epub 2003 Nov 6. Hum Genet. 2004. PMID: 14605873

3

Dystonia as a presenting sign of spinocerebellar ataxia type 1.

Wu YR, Lee-Chen GJ, Lang AE, Chen CM, Lin HY, Chen ST. Wu YR, et al. Among authors: chen st, chen cm. Mov Disord. 2004 May;19(5):586-7. doi: 10.1002/mds.10708. Mov Disord. 2004. PMID: 15133826

4

Markedly asymmetrical parkinsonism as a leading feature of adult-onset Huntington's disease.

Wang SC, Lee-Chen GJ, Wang CK, Chen CM, Tang LM, Wu YR. Wang SC, et al. Among authors: chen cm. Mov Disord. 2004 Jul;19(7):854-856. doi: 10.1002/mds.20093. Mov Disord. 2004. PMID: 15254954

5

Phenotypic features and genetic findings in 2 chinese families with Miyoshi distal myopathy.

Ro LS, Lee-Chen GJ, Lin TC, Wu YR, Chen CM, Lin CY, Chen ST. Ro LS, et al. Among authors: chen st, chen cm. Arch Neurol. 2004 Oct;61(10):1594-9. doi: 10.1001/archneur.61.10.1594. Arch Neurol. 2004. PMID: 15477515

6

Expanded trinucleotide repeats in the TBP/SCA17 gene mapped to chromosome 6q27 are associated with schizophrenia.

Chen CM, Lane HY, Wu YR, Ro LS, Chen FL, Hung WL, Hou YT, Lin CY, Huang SY, Chen IC, Soong BW, Li ML, Hsieh-Li HM, Su MT, Lee-Chen GJ. Chen CM, et al. Among authors: chen fl, chen ic. Schizophr Res. 2005 Oct 15;78(2-3):131-6. doi: 10.1016/j.schres.2005.06.018. Schizophr Res. 2005. PMID: 16054804

7

Recurrent cerebral venous thrombosis: an Arg359X mutation in the antithrombin gene in a Taiwanese family.

Chen CM, Lee-Chen GJ, Wu YR, Lin CY, Chen CJ, Chen IC, Ro LS. Chen CM, et al. Among authors: chen cj, chen ic. Thromb Res. 2006;118(2):235-40. doi: 10.1016/j.thromres.2005.07.019. Epub 2005 Sep 8. Thromb Res. 2006. PMID: 16154182 No abstract available.

8

Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan.

Fung HC, Chen CM, Hardy J, Singleton AB, Lee-Chen GJ, Wu YR. Fung HC, et al. Among authors: chen cm. Neurosci Lett. 2006 Feb 6;394(1):33-6. doi: 10.1016/j.neulet.2005.10.005. Epub 2005 Oct 27. Neurosci Lett. 2006. PMID: 16257123

9

Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease.

Fung HC, Chen CM, Hardy J, Hernandez D, Singleton A, Wu YR. Fung HC, et al. Among authors: chen cm. Mov Disord. 2006 Jun;21(6):880-1. doi: 10.1002/mds.20814. Mov Disord. 2006. PMID: 16511860

10

Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease.

Clarimon J, Scholz S, Fung HC, Hardy J, Eerola J, Hellstrom O, Chen CM, Wu YR, Tienari PJ, Singleton A. Clarimon J, et al. Among authors: chen cm. Am J Hum Genet. 2006 Jun;78(6):1082-4; author reply 1092-4. doi: 10.1086/504727. Am J Hum Genet. 2006. PMID: 16685660 Free PMC article. No abstract available.

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