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季康揚 (Kang-Yang Jih)


  • 學歷
    • 國立陽明大學 醫學院 醫學士
    • 美國密蘇里大學 生理學 博士
  • 經歷
    • 2022- 迄今 台灣神經罕見疾病學會 秘書長
    • 2021- 迄今 國立陽明交通大學生理學研究所 兼任助理教授
    • 2020- 迄今 臺北榮民總醫院神經內科 主治醫師
    • 2022- 迄今 國立陽明交通大學醫學系 導師
    • 2019- 2020 臺北榮民總醫院 神經內科總醫師
    • 2016- 2019 臺北榮民總醫院 神經內科住院醫師
    • 2015- 2016 臺北榮民總醫院 不分科住院醫師
    • 2010- 2011 美國密蘇里大學 生理學實驗助教
  • 醫療專長
    1. 周邊神經肌肉疾病
    2. 神經基因學之分子診斷
  • 證照



2019 臺北市醫師公會青年杏林獎

2017, 2018年度 臺北榮民總醫院最佳教學住院醫師

2013 Paul Cranefield Student Award (美國生理學會之年度獎項)



  1. Tsai MF, Jih KY, Shimizu H, Li M, Hwang TC. Optimization of the degenerated interfacial ATP binding site improves the function of disease-related mutant cystic fibrosis transmembrane conductance regulator (CFTR) channels. J Biol Chem. 2010;285(48):37663-37671.
  2. Jih KY, Li M, Hwang TC, Bompadre SG. The most common cystic fibrosis-associated mutation destabilizes the dimeric state of the nucleotide-binding domains of CFTR. J Physiol. 2011;589(Pt 11):2719-2731.
  3. Jih KY, Hwang TC. Nonequilibrium gating of CFTR on an equilibrium theme. Physiology (Bethesda). 2012;27(6):351-361.
  4. Jih KY, Sohma Y, Hwang TC. Nonintegral stoichiometry in CFTR gating revealed by a pore-lining mutation. J Gen Physiol. 2012;140(4):347-359.
  5. Jih KY, Sohma Y, Li M, Hwang TC. Identification of a novel post-hydrolytic state in CFTR gating. J Gen Physiol. 2012;139(5):359-370.
  6. Jih KY, Hwang TC. Vx-770 potentiates CFTR function by promoting decoupling between the gating cycle and ATP hydrolysis cycle. Proc Natl Acad Sci U S A. 2013;110(11):4404-4409.
  7. Lin WY, Jih KY, Hwang TC. A single amino acid substitution in CFTR converts ATP to an inhibitory ligand. J Gen Physiol. 2014;144(4):311-320.
  8. Jih KY, Lin WY, Sohma Y, Hwang TC. CFTR potentiators: from bench to bedside. Curr Opin Pharmacol. 2017;34:98-104.
  9. Jih KY, Chung CP, Chang YY, et al. Mutational analysis of CCM1, CCM2 and CCM3 in a Han Chinese cohort with multiple cerebral cavernous malformations in Taiwan. Clin Genet. 2018;94(3-4):389-390.
  10. Tsai PC, Liao YC, Jih KY, Soong BW, Lin KP, Lee YC. Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan. Neurobiol Aging. 2018;72:188 e181-188 e182.
  11. Chou CT, Soong BW, Lin KP, Tsai YS, Jih KY, Liao YC, et al. Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5. Ann Clin Transl Neurol. 2020;7(4):486-96.
  12. Jih KY, Lin KP, Tsai PC, Soong BW, Liao YC, Lee YC. Investigating TBP CAG/CAA trinucleotide repeat expansions in a Taiwanese cohort with ALS. Amyotroph Lateral Scler Frontotemporal Degener. 2020:1-6.
  13. Jih KY, Tsai PC, Tsai YS, Liao YC, Lee YC. Rapid progressive ALS in a patient with a DNAJC7 loss-of-function mutation. Neurol Genet. 2020;6(5):e503.
  14. Tsai YS, Lin KP, Jih KY, Tsai PC, Liao YC, Lee YC. Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variant. Ann Clin Transl Neurol. 2020;7(6):965-71.
  15. Jih KY, Chou YT, Tsai PC, et al. Analysis of NOTCH2NLC GGC repeat expansion in Taiwanese patients with amyotrophic lateral sclerosis. Neurobiol Aging 2021;108:210-12.
  16. Liao YC, Chang FP, Huang HW, Chen TB, Chou YT, Hsu SL, Jih KY, Liu YH et al. GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies. Neurology 98.2 (2022): e199-e206.
  17. Tsai PC, Jih KY, Shen TY, et al. Genetic and Functional Analysis of Glycosyltransferase 8 Domain-Containing Protein 1 in Taiwanese Patients With Amyotrophic Lateral Sclerosis. Neurol Genet 2021;7(6):e627.
  18. Hsu SL, Jih KY, Lin KP, et al. Assessing the NOTCH2NLC GGC repeat expansion in Taiwanese patients with hereditary spastic paraplegia. Parkinsonism Relat Disord 2022;96:43-44.