Hsu SL - Search Results

1

Biallelic DDHD2 mutations in patients with adult-onset complex hereditary spastic paraplegia.

Chou YT, Hsu SL, Tsai YS, Lu YJ, Yu KW, Wu HM, Liao YC, Lee YC. Chou YT, et al. Among authors: hsu sl. Ann Clin Transl Neurol. 2023 Sep;10(9):1603-1612. doi: 10.1002/acn3.51850. Epub 2023 Jul 7. Ann Clin Transl Neurol. 2023. PMID: 37420318 Free PMC article.

2

MPZ mutation G123S characterization: evidence for a complex pathogenesis in CMT disease.

Lee YC, Yu CT, Lin KP, Chang MH, Hsu SL, Liu YF, Lu YC, Soong BW. Lee YC, et al. Among authors: hsu sl. Neurology. 2008 Jan 22;70(4):273-7. doi: 10.1212/01.wnl.0000296828.66915.bf. Neurology. 2008. PMID: 18209201

3

Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegia.

Hsu SL, Lu YJ, Tsai YS, Chao HC, Fuh JL, Liao YC, Lee YC. Hsu SL, et al. J Formos Med Assoc. 2022 Jan;121(1 Pt 1):126-133. doi: 10.1016/j.jfma.2021.02.005. Epub 2021 Feb 24. J Formos Med Assoc. 2022. PMID: 33637369 Free article.

4

Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan.

Hsu SL, Hsueh HW, Chen SY, Chang YY, Tan S, Hong CT, Tsai YS, Yu KW, Wu HM, Liao YC, Soong BW, Hu CJ, Lan MY, Lee YC. Hsu SL, et al. Parkinsonism Relat Disord. 2021 Jun;87:87-91. doi: 10.1016/j.parkreldis.2021.05.004. Epub 2021 May 11. Parkinsonism Relat Disord. 2021. PMID: 34015694

5

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. 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

6

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: hsu sl. Neurology. 2022 Jan 11;98(2):e199-e206. doi: 10.1212/WNL.0000000000013008. Epub 2021 Oct 21. Neurology. 2022. PMID: 34675106

7

Assessing the NOTCH2NLC GGC repeat expansion in Taiwanese patients with hereditary spastic paraplegia.

Hsu SL, Jih KY, Lin KP, Liao YC, Lee YC. Hsu SL, et al. Parkinsonism Relat Disord. 2022 Mar;96:43-44. doi: 10.1016/j.parkreldis.2022.02.004. Epub 2022 Feb 13. Parkinsonism Relat Disord. 2022. PMID: 35180462

8

Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia.

Hsu SL, Liao YC, Lin KP, Lin PY, Yu KW, Tsai YS, Guo YC, Lee YC. Hsu SL, et al. Parkinsonism Relat Disord. 2022 Oct;103:144-149. doi: 10.1016/j.parkreldis.2022.09.001. Epub 2022 Sep 16. Parkinsonism Relat Disord. 2022. PMID: 36155026

9

Monogenic Causes in Familial Stroke Across Intracerebral Hemorrhage and Ischemic Stroke Subtypes Identified by Whole-Exome Sequencing.

Chang LH, Chi NF, Chen CY, Lin YS, Hsu SL, Tsai JY, Huang HC, Lin CJ, Chung CP, Tung CY, Jeng CJ, Lee YC, Liu YT, Lee IH. Chang LH, et al. Among authors: hsu sl. Cell Mol Neurobiol. 2023 Aug;43(6):2769-2783. doi: 10.1007/s10571-022-01315-3. Epub 2022 Dec 29. Cell Mol Neurobiol. 2023. PMID: 36580209 Free PMC article.

10

Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia.

Fang SY, Chou YT, Hsu KC, Hsu SL, Yu KW, Tsai YS, Liao YC, Tsai PC, Lee YC. Fang SY, et al. Among authors: hsu kc, hsu sl. Ann Clin Transl Neurol. 2023 Mar;10(3):353-362. doi: 10.1002/acn3.51724. Epub 2023 Jan 6. Ann Clin Transl Neurol. 2023. PMID: 36607129 Free PMC article. Review.

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