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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
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.
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.
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.
189 results