Wu YR - Search Results

1

Coexistence of pernicious anemia and myasthenia gravis--a rare combination of autoimmune diseases in Taiwan.

Chang KH, Lyu RK, Ro LS, Wu YR, Chen CM. Chang KH, et al. Among authors: wu yr. J Formos Med Assoc. 2006 Nov;105(11):946-9. doi: 10.1016/S0929-6646(09)60181-9. J Formos Med Assoc. 2006. PMID: 17098697 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

A longitudinal cardiovascular autonomic function study in mild Guillain-Barré syndrome.

Lyu RK, Tang LM, Hsu WC, Chen ST, Chang HS, Wu YR. Lyu RK, et al. Among authors: wu yr. Eur Neurol. 2002;47(2):79-84. doi: 10.1159/000047957. Eur Neurol. 2002. PMID: 11844895

5

Cardiovascular autonomic function and sympathetic skin response in chronic inflammatory demyelinating polyradiculoneuropathy.

Lyu RK, Tang LM, Wu YR, Chen ST. Lyu RK, et al. Among authors: wu yr. Muscle Nerve. 2002 Nov;26(5):669-72. doi: 10.1002/mus.10251. Muscle Nerve. 2002. PMID: 12402289

6

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

7

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.

8

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

9

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

10

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

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