Chang HC - Search Results

1

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan.

Di Fonzo A, Wu-Chou YH, Lu CS, van Doeselaar M, Simons EJ, Rohé CF, Chang HC, Chen RS, Weng YH, Vanacore N, Breedveld GJ, Oostra BA, Bonifati V. Di Fonzo A, et al. Among authors: chang hc. Neurogenetics. 2006 Jul;7(3):133-8. doi: 10.1007/s10048-006-0041-5. Epub 2006 Apr 22. Neurogenetics. 2006. PMID: 16633828

2

Acanthocytosis and spinocerebellar degeneration: a new association?

Tsai CH, Chen RS, Chang HC, Lu CS, Liao KK. Tsai CH, et al. Among authors: chang hc. Mov Disord. 1997 May;12(3):456-9. doi: 10.1002/mds.870120333. Mov Disord. 1997. PMID: 9159749 No abstract available.

3

Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2.

Lu CS, Wu Chou YH, Yen TC, Tsai CH, Chen RS, Chang HC. Lu CS, et al. Among authors: chang hc. Mov Disord. 2002 Sep;17(5):1046-51. doi: 10.1002/mds.10243. Mov Disord. 2002. PMID: 12360557

4

The parkinsonian phenotype of spinocerebellar ataxia type 2.

Lu CS, Wu Chou YH, Kuo PC, Chang HC, Weng YH. Lu CS, et al. Among authors: chang hc. Arch Neurol. 2004 Jan;61(1):35-8. doi: 10.1001/archneur.61.1.35. Arch Neurol. 2004. PMID: 14732617

5

99mTc-TRODAT-1 imaging of multiple system atrophy.

Lu CS, Weng YH, Chen MC, Chen RS, Tzen KY, Wey SP, Ting G, Chang HC, Yen TC. Lu CS, et al. Among authors: chang hc. J Nucl Med. 2004 Jan;45(1):49-55. J Nucl Med. 2004. PMID: 14734673 Free article. Clinical Trial.

6

Imaging early-stage corticobasal degeneration with [99mTc]TRODAT-1 SPET.

Lai SC, Weng YH, Yen TC, Tsai CC, Chang HC, Wey SP, Ting G, Lu CS. Lai SC, et al. Among authors: chang hc. Nucl Med Commun. 2004 Apr;25(4):339-45. doi: 10.1097/00006231-200404000-00005. Nucl Med Commun. 2004. PMID: 15097807

7

The parkinsonian phenotype of spinocerebellar ataxia type 3 in a Taiwanese family.

Lu CS, Chang HC, Kuo PC, Liu YL, Wu WS, Weng YH, Yen TC, Chou YH. Lu CS, et al. Among authors: chang hc. Parkinsonism Relat Disord. 2004 Aug;10(6):369-73. doi: 10.1016/j.parkreldis.2004.03.009. Parkinsonism Relat Disord. 2004. PMID: 15261879

8

PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations.

Hatano Y, Sato K, Elibol B, Yoshino H, Yamamura Y, Bonifati V, Shinotoh H, Asahina M, Kobayashi S, Ng AR, Rosales RL, Hassin-Baer S, Shinar Y, Lu CS, Chang HC, Wu-Chou YH, Ataç FB, Kobayashi T, Toda T, Mizuno Y, Hattori N. Hatano Y, et al. Among authors: chang hc. Neurology. 2004 Oct 26;63(8):1482-5. doi: 10.1212/01.wnl.0000142258.29304.fe. Neurology. 2004. PMID: 15505170

9

Pallidotomy effect on the cortical excitability in patients with severe Parkinson's disease.

Tsai CH, Chang FC, Lu CS, Lee ST, Huang YT, Lu MK, Chen RS, Wu T, Lee JD, Weng YH, Chang HC. Tsai CH, et al. Among authors: chang fc, chang hc. Mov Disord. 2005 Apr;20(4):463-470. doi: 10.1002/mds.20344. Mov Disord. 2005. PMID: 15593137

10

Taiwanese cases of SCA2 are derived from a single founder.

Momeni P, Lu CS, Chou YH, Chang HC, Chen RS, Chen CC, Hsu JT, Singleton A, Hardy J. Momeni P, et al. Among authors: chang hc. Mov Disord. 2005 Dec;20(12):1633-6. doi: 10.1002/mds.20638. Mov Disord. 2005. PMID: 16078202

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