Kuo SH - Search Results

1

Misfolded GBA/β-glucocerebrosidase impairs ER-quality control by chaperone-mediated autophagy in Parkinson disease.

Kuo SH, Tasset I, Cuervo AM, Sulzer D. Kuo SH, et al. Autophagy. 2022 Dec;18(12):3050-3052. doi: 10.1080/15548627.2022.2071383. Epub 2022 May 6. Autophagy. 2022. PMID: 35482760 Free PMC article.

2

Mitochondrial dysfunction and mitophagy defect triggered by heterozygous GBA mutations.

Li H, Ham A, Ma TC, Kuo SH, Kanter E, Kim D, Ko HS, Quan Y, Sardi SP, Li A, Arancio O, Kang UJ, Sulzer D, Tang G. Li H, et al. Among authors: kuo sh. Autophagy. 2019 Jan;15(1):113-130. doi: 10.1080/15548627.2018.1509818. Epub 2018 Oct 12. Autophagy. 2019. PMID: 30160596 Free PMC article.

3

Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations.

Alcalay RN, Levy OA, Waters CC, Fahn S, Ford B, Kuo SH, Mazzoni P, Pauciulo MW, Nichols WC, Gan-Or Z, Rouleau GA, Chung WK, Wolf P, Oliva P, Keutzer J, Marder K, Zhang X. Alcalay RN, et al. Among authors: kuo sh. Brain. 2015 Sep;138(Pt 9):2648-58. doi: 10.1093/brain/awv179. Epub 2015 Jun 27. Brain. 2015. PMID: 26117366 Free PMC article.

4

SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease.

Alcalay RN, Mallett V, Vanderperre B, Tavassoly O, Dauvilliers Y, Wu RYJ, Ruskey JA, Leblond CS, Ambalavanan A, Laurent SB, Spiegelman D, Dionne-Laporte A, Liong C, Levy OA, Fahn S, Waters C, Kuo SH, Chung WK, Ford B, Marder KS, Kang UJ, Hassin-Baer S, Greenbaum L, Trempe JF, Wolf P, Oliva P, Zhang XK, Clark LN, Langlois M, Dion PA, Fon EA, Dupre N, Rouleau GA, Gan-Or Z. Alcalay RN, et al. Among authors: kuo sh. Mov Disord. 2019 Apr;34(4):526-535. doi: 10.1002/mds.27642. Epub 2019 Feb 20. Mov Disord. 2019. PMID: 30788890 Free PMC article.

5

The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease.

Chan AY, Baum L, Tang NL, Lau CY, Ng PW, Hui KF, Mizuno Y, Kwan JY, Mok VC, Kuo SH. Chan AY, et al. Among authors: kuo sh. J Clin Neurosci. 2013 May;20(5):761-2. doi: 10.1016/j.jocn.2012.05.052. Epub 2013 Mar 20. J Clin Neurosci. 2013. PMID: 23522931 Free PMC article.

6

The Natural History of Depression in Parkinson's Disease within 30-Month Follow-Up.

Xu YY, Kuo SH, Liang Z, Xu H, Feng WR, Yu CY, Liu WG. Xu YY, et al. Among authors: kuo sh. Parkinsons Dis. 2015;2015:362892. doi: 10.1155/2015/362892. Epub 2015 Feb 1. Parkinsons Dis. 2015. PMID: 25722914 Free PMC article.

7

Coenzyme Q10 as a Peripheral Biomarker for Multiple System Atrophy.

Kuo SH, Quinzii CM. Kuo SH, et al. JAMA Neurol. 2016 Aug 1;73(8):917-9. doi: 10.1001/jamaneurol.2016.1810. JAMA Neurol. 2016. PMID: 27367485 Free PMC article. No abstract available.

8

Abnormal Vertical Eye Movements as a Clue for Diagnosis of Niemann-Pick Type C.

Gupta DK, Blanco-Palmero VA, Chung WK, Kuo SH. Gupta DK, et al. Among authors: kuo sh. Tremor Other Hyperkinet Mov (N Y). 2018 May 29;8:560. doi: 10.7916/D8XS7BGD. eCollection 2018. Tremor Other Hyperkinet Mov (N Y). 2018. PMID: 29971198 Free PMC article.

9

Association of Tef polymorphism with depression in Parkinson disease.

Hua P, Liu W, Kuo SH, Zhao Y, Chen L, Zhang N, Wang C, Guo S, Wang L, Xiao H, Kwan JY, Wu T. Hua P, et al. Among authors: kuo sh. Mov Disord. 2012 Nov;27(13):1694-7. doi: 10.1002/mds.25195. Epub 2012 Nov 8. Mov Disord. 2012. PMID: 23138696 Free PMC article.

10

Multiple system atrophy and repeat expansions in C9orf72--reply.

Goldman JS, Kuo SH. Goldman JS, et al. Among authors: kuo sh. JAMA Neurol. 2014 Sep;71(9):1191-2. doi: 10.1001/jamaneurol.2014.1811. JAMA Neurol. 2014. PMID: 25200544 Free PMC article. No abstract available.

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