Hsiao CT - Search Results

1

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.

2

C9ORF72 repeat expansion is not a significant cause of late onset cerebellar ataxia syndrome.

Hsiao CT, Tsai PC, Liao YC, Lee YC, Soong BW. Hsiao CT, et al. J Neurol Sci. 2014 Dec 15;347(1-2):322-4. doi: 10.1016/j.jns.2014.10.042. Epub 2014 Nov 6. J Neurol Sci. 2014. PMID: 25467142

3

Acute simultaneous multiple lacunar infarcts as the initial presentation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Hsiao CT, Chen YC, Liu YT, Soong BW, Lee YC. Hsiao CT, et al. J Chin Med Assoc. 2015 Jul;78(7):424-6. doi: 10.1016/j.jcma.2015.01.007. Epub 2015 May 7. J Chin Med Assoc. 2015. PMID: 25959358 Free article.

4

[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.

5

Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles.

Liao YC, Hsiao CT, Fuh JL, Chern CM, Lee WJ, Guo YC, Wang SJ, Lee IH, Liu YT, Wang YF, Chang FC, Chang MH, Soong BW, Lee YC. Liao YC, et al. Among authors: hsiao ct. PLoS One. 2015 Aug 26;10(8):e0136501. doi: 10.1371/journal.pone.0136501. eCollection 2015. PLoS One. 2015. PMID: 26308724 Free PMC article.

6

Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosis.

Tsai PC, Liu YC, Lin KP, Liu YT, Liao YC, Hsiao CT, Soong BW, Yip PK, Lee YC. Tsai PC, et al. Among authors: hsiao ct. Neurobiol Aging. 2016 Apr;40:191.e11-191.e16. doi: 10.1016/j.neurobiolaging.2015.12.022. Epub 2016 Jan 5. Neurobiol Aging. 2016. PMID: 26804609

7

Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary Neuropathy.

Hsiao CT, Tsai PC, Lin CC, Liu YT, Huang YH, Liao YC, Huang HW, Lin KP, Soong BW, Lee YC. Hsiao CT, et al. PLoS One. 2016 Jan 27;11(1):e0147677. doi: 10.1371/journal.pone.0147677. eCollection 2016. PLoS One. 2016. PMID: 26815532 Free PMC article.

8

Spinocerebellar ataxia type 36 in the Han Chinese.

Lee YC, Tsai PC, Guo YC, Hsiao CT, Liu GT, Liao YC, Soong BW. Lee YC, et al. Among authors: hsiao ct. Neurol Genet. 2016 Apr 12;2(3):e68. doi: 10.1212/NXG.0000000000000068. eCollection 2016 Jun. Neurol Genet. 2016. PMID: 27123487 Free PMC article.

9

A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy.

Tsai PC, Soong BW, Mademan I, Huang YH, Liu CR, Hsiao CT, Wu HT, Liu TT, Liu YT, Tseng YT, Lin KP, Yang UC, Chung KW, Choi BO, Nicholson GA, Kennerson ML, Chan CC, De Jonghe P, Cheng TH, Liao YC, Züchner S, Baets J, Lee YC. Tsai PC, et al. Among authors: hsiao ct. Brain. 2017 May 1;140(5):1252-1266. doi: 10.1093/brain/awx058. Brain. 2017. PMID: 28369220 Free PMC article.

10

Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy.

Liao YC, Tsai PC, Lin TS, Hsiao CT, Chao NC, Lin KP, Lee YC. Liao YC, et al. Among authors: hsiao ct. Sci Rep. 2017 Nov 10;7(1):15363. doi: 10.1038/s41598-017-14771-5. Sci Rep. 2017. PMID: 29127354 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

177 results

Search Page