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蕭丞宗 (Cheng-Tsung Hsiao)

蕭丞宗(Cheng-Tsung Hsiao)圖 掛號

[簡介]

  • 學歷
    • 國立臺灣大學 生理學研究所 博士
    • 國防醫學院 醫學士
  • 經歷
    現職：
    • 2020- 迄今 臺北榮民總醫院神經內科 周邊神經科 主治醫師
    • 2022- 迄今 國立陽明交通大學神經學科 助理教授
    經歷：
    • 2018- 2020 臺北榮民總醫院神經內科 特約醫師
    • 2018- 2018 日本名古屋大學醫院腦神經科 進修醫師
    • 2016- 2020 臺北榮民總醫院桃園分院神經內科 主治醫師
    • 2011- 2016 臺北榮民總醫院神經內科 住院醫師
    • 2010- 2011 臺中榮民總醫院內科部 住院醫師
    • - 台灣神經罕見疾病學會第一屆第二任秘書長
  • 醫療專長
    1. 周邊神經肌肉疾病（末梢神經病變、家族遺傳性神經病變、慢性疼痛、肌肉病變、肌強直症、肌無力症）
    2. 神經退化性疾病（小腦萎縮症、甘迺迪氏症、漸凍症、亨丁頓氏舞蹈症、帕金森氏症、顫抖症、腦白質病變、失智症）
    3. 家族性腦中風
    4. 神經電生理檢查
    5. 神經基因學之分子診斷

[著作]

研究方向：

神經基因學之臨床與分子研究（小腦萎縮症、家族性周邊神經病變、甘迺迪氏症、家族性腦中風）；細胞電生理與分子生物學研究；離子通道蛋白相關疾病之研究...等。

 

得獎紀錄：

2020

國立臺灣大學醫學院研究生優秀著作獎

2019

臺灣神經學會年輕學者獎

 

論文發表：

  1. YC Liao, FP Chang, HW Huang, TB Chen, YT Chou, SL Hsu, KY Jih, YH Liu, CT Hsiao, H Fukukda, T Mizuguchi, KP Lin, CK Lin, N Matsumoto, M Kennerson, YC Lee. (2022, Jan). GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies. Neurology, 98(2):e199-e206.
  2. CT Hsiao, TF Tropea, SJ Fu, TM Bardakjian, P Gonzalez-Alegre, BW Soong, CY Tang*, CJ Jeng*. 2021 July. Rare Gain-of-Function KCND3 Variant Associated with Cerebellar Ataxia, Parkinsonism, Cognitive Dysfunction, and Brain Iron Accumulation. Int. J. Mol. Sci. 8247.
     
  3. G Zanni*, CT Hsiao*, SJ Fu, CY Tang, A Capuano, L Bosco, F Graziola, E Bellacchio, S Servidei, G Primiano, BW Soong, CJ Jeng. 2021, May. Novel KCND3 Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt KV4.3 Protein Expression and K+ Currents with Variable Effects on Channel Properties. Int. J. Mol. Sci. 4986.
     
  4. SJ Fu, MC Hu, CT Hsiao, AT Cheng, TY Chen, CJ Jeng, CY Tang. 2021 May. Regulation of ClC-2 Chloride Channel Proteostasis by Molecular Chaperones: Correction of Leukodystrophy-Associated Defect. Int. J. Mol. Sci. 5859.
     
  5. SJ Fu, MC Hu, YJ Peng, HY Fang, CT Hsiao, TY Chen, CJ Jeng, CY Tang*. 2020 May. CUL4-DDB1-CRBN E3 Ubiquitin Ligase Regulates Proteostasis of ClC-2 Chloride Channels: Implication for Aldosteronism and Leukodystrophy. Cells. 1332.
     
  6. HH Chiu, CT Hsiao, YS Tsai, YC Liao, YC Lee, BW Soong. 2020 May. Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan. Cerebellum. 544-549.
     
  7. CJ Jeng, SJ Fu, CY You, YJ Peng, CT Hsiao, TY Chen, CY Tang*. 2020 Feb. Defective Gating and Proteostasis of Human ClC-1 Chloride Channel: Molecular Pathophysiology of Myotonia Congenita. Frontiers in Neurology. 76. (Review)
     
  8. CT Hsiao, SJ Fu, YT Liu, YH Lu, CY Zhong, CY Tang, BW Soong, CJ Jeng*. 2019 Nor. Novel SCA19/22-associated KCND3 mutations disrupt human KV4.3 protein biosynthesis and channel gating. Human mutation. 2088-2107.
     
  9. KL Lai, YC Liao, PC Tsai, CT Hsiao, BW Soong, YC Lee*. 2019 Sep. Investigating PUM1 mutations in a Taiwanese cohort with cerebellar ataxia. Parkinsonism Related Disorders. 220-223.
     
  10. CT Hsiao, YT Liu, YC Liao, TY Hsu, YC Lee, BW Soong*. 2018 Feb. Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxias. PLoS One. e0187503.
     
  11. YC Liao, PC Tsai, TS Lin, CT Hsiao, NC Chao, KP Lin, YC Lee*. 2017 Nov. Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy. Scientific Report. 15363.
     
  12. PC Tsai, BW Soong, I Mademan, YH Huang, CR Liu, CT Hsiao, HT Wu, TT Liu, YT Liu, YT Tseng, KP Lin, UC Yang, KW Chung, BO Choi, GA Nicholson, ML Kennerson, CC Chan, PD Jonghe, TH Cheng, YC Liao, S Züchner, J Baets, YC Lee*. 2017 May. A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy. Brain. 1252-1266.
     
  13. Chen YH, Lee YC, Tsai YS, Guo YC, Hsiao CT, Tsai PC, Huang JA, Liao YC, Soong BW*. 2017 May. Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia. PLoS One. e0177296.
     
  14. YC Lee, PC Tsai, YC Guo, CT Hsiao, GT Liu, YC Liao, BW Soong*. 2016 Jun. Spinocerebellar ataxia type 36 in the Han Chinese. Neurol Genet. e68.
     
  15. PC Tsai, YC Liu, KP Lin, YT Liu, YC Liao, CT Hsiao, BW Soong, PK Yip, YC Lee*. 2016 Apr. Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosis. Neurobiol Aging. 191.e11-6.
     
  16. CT Hsiao, PC Tsai, CC Lin, YT Liu, YH Huang, YC Liao, HW Huang, KP Lin, BW Soong, YC Lee*. 2016 Jan. Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary Neuropathy. PLoS One. e0147677.
     
  17. YC Liao#, CT Hsiao#, JL Fuh, CM Chern, WJ Lee, YC Guo, SJ Wang, IH Lee, YT Liu, YF Wang, FC Chang, MH Chang, BW Soong, YC Lee*. 2015 Aug. Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles. PLoS One. e0136501.
     
  18. CT Hsiao, YC Chen, YT Liu, BW Soong, YC Lee*. 2015 Jul. Acute simultaneous multiple lacunar infarcts as the initial presentation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. J Chin Med Assoc. 424-6.
     
  19. CT Hsiao, PC Tsai, YC Liao, YC Lee, BW Soong*. 2014 Dec. C9ORF72 repeat expansion is not a significant cause of late onset cerebellar ataxia syndrome. J Neurol Sci. 322-4.
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