Wu YR - Search Results

1

Functional properties of LRRK2 mutations in Taiwanese Parkinson disease.

Chang KH, Chen CM, Lin CH, Chang WT, Jiang PR, Hsiao YC, Wu YR, Lee-Chen GJ. Chang KH, et al. Among authors: wu yr. J Formos Med Assoc. 2017 Mar;116(3):197-204. doi: 10.1016/j.jfma.2016.04.009. Epub 2016 Jul 14. J Formos Med Assoc. 2017. PMID: 27423549 Free article.

2

Rimmed, vacuolar distal myopathy in two Taiwanese siblings.

Wu YR, Chen ST, So LS, Chen CJ. Wu YR, et al. J Formos Med Assoc. 1995 Dec;94(12):750-3. J Formos Med Assoc. 1995. PMID: 8541738

3

Vocal cord paralysis as an initial sign of multiple system atrophy in the central nervous system.

Wu YR, Chen CM, Ro LS, Chen ST, Tang LM. Wu YR, et al. J Formos Med Assoc. 1996 Oct;95(10):804-6. J Formos Med Assoc. 1996. PMID: 8961681

4

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. Hum Genet. 2004 Feb;114(3):236-41. doi: 10.1007/s00439-003-1050-1. Epub 2003 Nov 6. Hum Genet. 2004. PMID: 14605873

5

The use of evoked potentials for clinical correlation and surgical outcome in cervical spondylotic myelopathy with intramedullary high signal intensity on MRI.

Lyu RK, Tang LM, Chen CJ, Chen CM, Chang HS, Wu YR. Lyu RK, et al. Among authors: wu yr. J Neurol Neurosurg Psychiatry. 2004 Feb;75(2):256-61. J Neurol Neurosurg Psychiatry. 2004. PMID: 14742600 Free PMC article. Clinical Trial.

6

Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.

Wu YR, Lin HY, Chen CM, Gwinn-Hardy K, Ro LS, Wang YC, Li SH, Hwang JC, Fang K, Hsieh-Li HM, Li ML, Tung LC, Su MT, Lu KT, Lee-Chen GJ. Wu YR, et al. Clin Genet. 2004 Mar;65(3):209-14. doi: 10.1111/j.0009-9163.2004.00213.x. Clin Genet. 2004. PMID: 14756671

7

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. Mov Disord. 2004 May;19(5):586-7. doi: 10.1002/mds.10708. Mov Disord. 2004. PMID: 15133826

8

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: wu yr. Mov Disord. 2004 Jul;19(7):854-856. doi: 10.1002/mds.20093. Mov Disord. 2004. PMID: 15254954

9

DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients.

Wang CK, Wu YR, Hwu WL, Chen CM, Ro LS, Chen ST, Gwinn-Hardy K, Yang CC, Wu RM, Chen TF, Wang HC, Chao MC, Chiu MJ, Lu CJ, Lee-Chen GJ. Wang CK, et al. Among authors: wu yr, wu rm. Eur Neurol. 2004;52(2):96-100. doi: 10.1159/000079938. Epub 2004 Jul 22. Eur Neurol. 2004. PMID: 15273431

10

Sensory neuropathy as the initial manifestation of multiple system atrophy.

Wu YR, Chen CM, Ro LS, Lyu RK, Tang LM. Wu YR, et al. J Formos Med Assoc. 2004 Sep;103(9):727-30. J Formos Med Assoc. 2004. PMID: 15361949

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