李宜中醫師詳細介紹

哈佛醫學院附屬Brigham and Women’s Hospital完成分子生物學進修

國立陽明大學臨床醫學研究所博士班

國立陽明大學醫學士

-迄今臺北榮民總醫院神經醫學中心周邊神經科主治醫師

-迄今國立陽明交通大學神經學科兼任教授

-迄今臺灣神經醫學會理事

-迄今美國神經醫學院院士(Fellow, American Academy of Neurology)

-臺北榮民總醫院神經醫學中心周邊神經科 科主任

基因診斷

神經退化及遺傳疾病 (如遺傳性腦中風、運動神經元疾病、CMT、巴金森氏症、小腦萎縮症）

周邊神經病變

Hsu SL, Liao YC, Wu CH, Change FC, Chen YL, Lai KL, Chung CP, Chen SP*, Lee YC*. Impaired Cerebral Interstitial Fluid Dynamics in CADASIL. Brain Communications 2024;6(1): fcad349.

Lin X*, Jiang JY, Hong DJ, Lin KJ, Chen YJ, Qiu YS, Wang Z, Liao YC, Yang K, Shi Y, Wang MW, Hsu SL, Hong S, Zeng YH, Chen XC, Wang N, Lee YC*, Chen WJ*. Biallelic COQ4 variants in hereditary spastic paraplegia: clinical and molecular characterization. Movement disorders 2023Nov 28. doi: 10.1002/mds.29664.

Chou YT, Hsu SL, Tsai YS, Lu YJ, Yu KW, Wu HM, Liao YC, Lee YC*. Biallelic DDHD2 mutations in patients with adult-onset complex hereditary spastic paraplegia. Ann Clin Transl Neurol 2023 Sep;10(9):1603-1612.

Liao YC, Wei CY, Chang FP, Chou YT, Hsu SL, Chung CP, Mizuguchi T, Matsumoto N, Yet SF, Lee YC*. NOTCH2NLC GGC repeat expansion in patients with vascular leukoencephalopathy. Stroke 2023;54(5):1236-45.

Fang SY, Chou YT, Hsu KC, Hsu SL, Yu KW, Tsai YS, Liao YC, Lee YC*. Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia. Ann Clin Transl Neurol 2023;10(3):353-62.

Hsu SL, Liao YC, Lin KP, Lin PY, Yu KW, Tsai YS, Guo YC, Lee YC*. Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia. Parkinsonism Relat Disord 2022 Sep 16;103:144-149.

Liu YH, Chou YT, Chang FP, Lee WJ, Guo YC, Chou CT, Huang HC, Mizuguchi T, Chou CC, Yu HY, Yu KW, Wu HM, Tsai PC, Matsumoto N, Lee YC*, Liao YC*. Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy. Brain 2022 Sep 14;145(9):3010-21.

Wang YF, Liao YC, Tzeng YS, Chen SP, Lirng JF, Fuh JL, Chen WT, Lai KL, Lee YC*, Wang SJ*. Mutation screening and association analysis of NOTCH3 p.R544C in patients with migraine with or without aura. Cephalalgia 2022 Aug;42(9):888-898.

Liao YC, Chang FP, Huang HW, Chen TB, Chou YT, Hsu SL, Jih K, Liu YH, Hsiao CT, Fukukda H, Mizuguchi T, Lin KK, Lin CK, Matsumoto N, Kennerson M, Lee YC*. GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies. Neurology 2022;98(2):e199-206.

Hsu SL, Chen YH, Chou CT, Chou YT, Tsai YS, Hsiao CT, Liao YC*, Lee YC*. Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype. Parkinsonism Relat Disord 2021;92:7-12.

Tsai PC, Fuh JL, Yang CC, Chang A, Lien LM, Wang PN, Lai KL, Tsai YS, Lee YC*, Liao YC. Clinical and genetic characterization of CSF1R-related leukoencephalopathy in a Taiwanese cohort with adult-onset leukoencephalopathy. Ann Clin Transl Neurol; 2021;8(11):2121-31.

Tsai PC, Jih KY, Shen TY, Liu YH, Lin KP, Liao YC, Lee YC*. Genetic and functional analysis of GLT8D1 in Taiwanese patients with amyotrophic lateral sclerosis. Neurol Genet 2021;7(6)e627

Chiang HL, Fuh JL, Tsai YS, Soong BW, Liao YC, Lee YC*. Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxia. J Neurol Sci 2021;428:117600.

Liao YC, Hu YC, Chung CP, Wang YF, Guo YC, Tsai YS, LeeYC*. Intracerebral hemorrhage in CADASIL: prevalence, clinical and neuroimaging features and risk factors. Stroke 2021;52(3):985-93.

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.

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 Jun;7(6):965-971.

Chou CT, Soong BW, Lin KP, Tsai YS, Jih KY, Liao YC, Lee YC*. Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5.Ann Clin Transl Neurol. 2020;7(4):486-496.

Lee YC, Chung CP, Chang MH, Wang SJ, Liao YC*. NOTCH3 cysteine-altering variant is an important risk factor for stroke in Taiwanese population. Neurology 2020;94(1):e87-e96.

Hsu YH, Lin KP, Guo YC, Tsai YS, Liao YC, Lee YC*. Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in Taiwan. Ann Clin Transl Neurol 2019;6(6): 1090-1101.

Chao HC, Liao YC, Liu YT, Guo YC, Chang FP, Lee YC*, KP Lin*. Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan. Ann Clin Transl Neurol 2019;6(5):913-922.