Cheng-Tsung Hsiao - Search Results

Year	Number of Results
2014	2
2015	2
2016	3
2017	4
2018	1
2019	2
2020	2
2021	5
2022	2
2023	3
2024	1

1

Defective Gating and Proteostasis of Human ClC-1 Chloride Channel: Molecular Pathophysiology of Myotonia Congenita.

Jeng CJ, Fu SJ, You CY, Peng YJ, Hsiao CT, Chen TY, Tang CY. Jeng CJ, et al. Among authors: hsiao ct. Front Neurol. 2020 Feb 11;11:76. doi: 10.3389/fneur.2020.00076. eCollection 2020. Front Neurol. 2020. PMID: 32117034 Free PMC article. Review.

2

[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].

Chen YC, Hsiao CT, Soong BW, Lee YC. Chen YC, et al. Among authors: hsiao ct. Acta Neurol Taiwan. 2014 Jun;23(2):64-74. Acta Neurol Taiwan. 2014. PMID: 26035923 Free article. Review. Chinese.

3

Reply to: Mitochondrial disorders are not spinocerebellar ataxias but may resemble them in some aspects.

Hsiao CT, Liao NY, Lee YC. Hsiao CT, et al. J Formos Med Assoc. 2023 Sep;122(9):967. doi: 10.1016/j.jfma.2023.06.024. Epub 2023 Jul 8. J Formos Med Assoc. 2023. PMID: 37429771 Free article. No abstract available.

4

Clinical and genetic characterization of NEFL-related neuropathy in Taiwan.

Chao HC, Hsiao CT, Lai KL, Tsai YS, Lin KP, Liao YC, Lee YC. Chao HC, et al. Among authors: hsiao ct. J Formos Med Assoc. 2023 Feb;122(2):132-138. doi: 10.1016/j.jfma.2022.08.008. Epub 2022 Aug 26. J Formos Med Assoc. 2023. PMID: 36031490 Free article.

5

GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies.

Liao YC, Chang FP, Huang HW, Chen TB, Chou YT, Hsu SL, Jih KY, Liu YH, Hsiao CT, Fukukda H, Mizuguchi T, Lin KP, Lin CK, Matsumoto N, Kennerson M, Lee YC. Liao YC, et al. Among authors: hsiao ct. Neurology. 2022 Jan 11;98(2):e199-e206. doi: 10.1212/WNL.0000000000013008. Epub 2021 Oct 21. Neurology. 2022. PMID: 34675106

6

Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia.

Liao NY, Lai KL, Liao YC, Hsiao CT, Lee YC. Liao NY, et al. Among authors: hsiao ct. J Formos Med Assoc. 2023 Oct;122(10):1028-1034. doi: 10.1016/j.jfma.2023.05.031. Epub 2023 Jun 11. J Formos Med Assoc. 2023. PMID: 37311680 Free article.

7

A missense mutation in human INSC causes peripheral neuropathy.

Yeh JY, Chao HC, Hong CL, Hung YC, Tzou FY, Hsiao CT, Li JL, Chen WJ, Chou CT, Tsai YS, Liao YC, Lin YC, Lin S, Huang SY, Kennerson M, Lee YC, Chan CC. Yeh JY, et al. Among authors: hsiao ct. EMBO Mol Med. 2024 Apr 8. doi: 10.1038/s44321-024-00062-w. Online ahead of print. EMBO Mol Med. 2024. PMID: 38589651 Free article.

8

Investigating PUM1 mutations in a Taiwanese cohort with cerebellar ataxia.

Lai KL, Liao YC, Tsai PC, Hsiao CT, Soong BW, Lee YC. Lai KL, et al. Among authors: hsiao ct. Parkinsonism Relat Disord. 2019 Sep;66:220-223. doi: 10.1016/j.parkreldis.2019.08.004. Epub 2019 Aug 7. Parkinsonism Relat Disord. 2019. PMID: 31422002

9

Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype.

Hsu SL, Chen YH, Chou CT, Chou YT, Tsai YS, Hsiao CT, Liao YC, Lee YC. Hsu SL, et al. Among authors: hsiao ct. Parkinsonism Relat Disord. 2021 Nov;92:7-12. doi: 10.1016/j.parkreldis.2021.10.006. Epub 2021 Oct 9. Parkinsonism Relat Disord. 2021. PMID: 34649108

10

Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia.

Chen YH, Lee YC, Tsai YS, Guo YC, Hsiao CT, Tsai PC, Huang JA, Liao YC, Soong BW. Chen YH, et al. Among authors: hsiao ct. PLoS One. 2017 May 8;12(5):e0177296. doi: 10.1371/journal.pone.0177296. eCollection 2017. PLoS One. 2017. PMID: 28481932 Free PMC article.

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