Lin CH - Search Results

1

Topographical metal burden correlates with brain atrophy and clinical severity in Wilson's disease.

Fan SP, Chen YF, Li CH, Kuo YC, Lee NC, Chien YH, Hwu WL, Tseng TC, Su TH, Hsu CT, Chen HL, Lin CH, Ni YH. Fan SP, et al. Among authors: lin ch. Neuroimage. 2024 Oct 1;299:120829. doi: 10.1016/j.neuroimage.2024.120829. Epub 2024 Sep 2. Neuroimage. 2024. PMID: 39233127 Free 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

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.

5

Clinical and electrophysiological characteristics of a type 1 sialidosis patient with a novel deletion mutation in NEU1 gene.

Fan SP, Lee NC, Lin CH. Fan SP, et al. Among authors: lin ch. J Formos Med Assoc. 2020 Jan;119(1 Pt 3):406-412. doi: 10.1016/j.jfma.2019.07.017. Epub 2019 Jul 29. J Formos Med Assoc. 2020. PMID: 31371146 Free article. Review.

6

Blood NfL: A biomarker for disease severity and progression in Parkinson disease.

Lin CH, Li CH, Yang KC, Lin FJ, Wu CC, Chieh JJ, Chiu MJ. Lin CH, et al. Among authors: lin fj. Neurology. 2019 Sep 10;93(11):e1104-e1111. doi: 10.1212/WNL.0000000000008088. Epub 2019 Aug 16. Neurology. 2019. PMID: 31420461

7

Antiviral Therapy in Patients With Chronic Hepatitis C Is Associated With a Reduced Risk of Parkinsonism.

Su TH, Yang HC, Tseng TC, Chou SW, Lin CH, Liu CH, Liu CJ, Chen CL, Kao JH. Su TH, et al. Among authors: lin ch. Mov Disord. 2019 Dec;34(12):1882-1890. doi: 10.1002/mds.27848. Epub 2019 Sep 10. Mov Disord. 2019. PMID: 31505068

8

Heterogeneous nonataxic phenotypes of spinocerebellar ataxia in a Taiwanese population.

Chen SJ, Lee NC, Chien YH, Hwu WL, Lin CH. Chen SJ, et al. Among authors: lin ch. Brain Behav. 2019 Oct;9(10):e01414. doi: 10.1002/brb3.1414. Epub 2019 Sep 16. Brain Behav. 2019. PMID: 31523939 Free PMC article.

9

Frontal variant of Alzheimer's disease with asymmetric presentation mimicking frontotemporal dementia: Case report and literature review.

Li CH, Fan SP, Chen TF, Chiu MJ, Yen RF, Lin CH. Li CH, et al. Among authors: lin ch. Brain Behav. 2020 Mar;10(3):e01548. doi: 10.1002/brb3.1548. Epub 2020 Jan 27. Brain Behav. 2020. PMID: 31989779 Free PMC article. Review.

10

Novel Phenotype of 6p25 Deletion Syndrome Presenting Juvenile Parkinsonism and Brain Calcification.

Fan SP, Lee NC, Lin CH. Fan SP, et al. Among authors: lin ch. Mov Disord. 2020 Aug;35(8):1457-1462. doi: 10.1002/mds.28079. Epub 2020 May 5. Mov Disord. 2020. PMID: 32369633

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