Lin CH - Search Results

1

Clinical Characteristics, Genetic Features, and Long-Term Outcome of Wilson's Disease in a Taiwanese Population: An 11-Year Follow-Up Study.

Fan SP, Kuo YC, Lee NC, Chien YH, Hwu WL, Huang YH, Lin HI, Tseng TC, Su TH, Tzeng SR, Hsu CT, Chen HL, Lin CH, Ni YH. Fan SP, et al. Among authors: lin ch, lin hi. J Mov Disord. 2023 May;16(2):168-179. doi: 10.14802/jmd.22161. Epub 2023 Mar 6. J Mov Disord. 2023. PMID: 36872857 Free PMC article.

2

Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.

Wu RM, Bounds R, Lincoln S, Hulihan M, Lin CH, Hwu WL, Chen J, Gwinn-Hardy K, Farrer M. Wu RM, et al. Among authors: lin ch. Arch Neurol. 2005 Jan;62(1):82-7. doi: 10.1001/archneur.62.1.82. Arch Neurol. 2005. PMID: 15642853

3

Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism.

Lin CH, Hwu WL, Chiang SC, Tai CH, Wu RM. Lin CH, et al. Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):434-8. doi: 10.1002/ajmg.b.30427. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17440947

4

Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism.

Lee MJ, Mata IF, Lin CH, Tzen KY, Lincoln SJ, Bounds R, Lockhart PJ, Hulihan MM, Farrer MJ, Wu RM. Lee MJ, et al. Among authors: lin ch. Mov Disord. 2009 Jan 15;24(1):104-8. doi: 10.1002/mds.22093. Mov Disord. 2009. PMID: 19006224

5

Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population.

Lin CH, Chen KH, Chen ML, Lin HI, Wu RM. Lin CH, et al. Among authors: lin hi. Neurobiol Aging. 2014 May;35(5):1212.e11-3. doi: 10.1016/j.neurobiolaging.2013.10.094. Epub 2013 Oct 29. Neurobiol Aging. 2014. PMID: 24239437

6

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.

Wu RM, Lin CH, Lin HI. Wu RM, et al. Among authors: lin ch, lin hi. Neurology. 2014 Jan 21;82(3):283. doi: 10.1212/WNL.0000000000000004. Neurology. 2014. PMID: 24446175 No abstract available.

7

Lack of c9orf72 repeat expansion in taiwanese patients with mixed neurodegenerative disorders.

Lin CH, Chen TF, Chiu MJ, Lin HI, Wu RM. Lin CH, et al. Among authors: lin hi. Front Neurol. 2014 Apr 28;5:59. doi: 10.3389/fneur.2014.00059. eCollection 2014. Front Neurol. 2014. PMID: 24803912 Free PMC article.

8

Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3β activity.

Lin CH, Lin HI, Chen ML, Lai TT, Cao LP, Farrer MJ, Wu RM, Chien CT. Lin CH, et al. Among authors: lin hi. Hum Mol Genet. 2016 May 15;25(10):1965-1978. doi: 10.1093/hmg/ddw068. Epub 2016 Feb 29. Hum Mol Genet. 2016. PMID: 26931464

9

Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort.

Lin HH, Wu RM, Lin HI, Chen ML, Tai CH, Lin CH. Lin HH, et al. Among authors: lin ch, lin hi. Neurobiol Aging. 2017 Feb;50:169.e3-169.e4. doi: 10.1016/j.neurobiolaging.2016.10.021. Epub 2016 Oct 21. Neurobiol Aging. 2017. PMID: 27838047

10

A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review.

Hsueh SJ, Lee NC, Yang SH, Lin HI, Lin CH. Hsueh SJ, et al. Among authors: lin ch, lin hi. BMC Neurol. 2017 Jan 6;17(1):2. doi: 10.1186/s12883-016-0781-2. BMC Neurol. 2017. PMID: 28056872 Free PMC article. Review.

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