廖翊筑醫師詳細介紹

高雄醫學大學醫學研究所博士

高雄醫學大學醫學遺傳所碩士

國立陽明大學醫學系畢業

-迄今臺北榮民總醫院神經醫學中心周邊神經科 科主任

-迄今國立陽明交通大學醫學院神經學科 教授

-迄今台灣神經免疫醫學會常務理事

-臺北榮民總醫院神經醫學中心周邊神經科 主治醫師

-高雄義大醫院神經科主治醫師

-台中榮總神經醫學中心主治醫師

-台灣頭痛學會第二屆至第五屆理事

-台灣神經學學會第十九屆理事

-臺北榮民總醫院神經內科住院醫師

遺傳性腦部小血管疾病

多發性硬化症

泛視神經脊髓炎

週邊神經病變

肌無力症

Chi-Ju Lin, Shih-Chieh Lin, Kai-Wei Yu, Wen-Yu Ou Yang, Yi-Chung Lee, Yi- Chu Liao (2023, Dec). Tumefactive Demyelination Lesions: Report on three cases. Acta Neurol Taiwan. 2024 Dec 30:33(4):195-200.

Yi-Chu Liao, Cheng-Yu Wei, Fu-Pang Chang, Ying-Tsen Chou, Shao-Lun Hsu, Chih-Ping Chung, Takeshi Mizuguchi, Naomichi Matsumoto,; Shaw-Fang Yet, Yi-Chung Lee (2023, May). NOTCH2NLC GGC Repeat Expansion in Patients With Vascular Leukoencephalopathy. Stroke, 54;1236-1245. (SCI, 16/212, Clinical Neurology).

Yumi Yamamoto*, Yi-Chu Liao*, Yi-Chung Lee, Masafumi Ihara, Jay Chol Choi (2023, Jan). Update on the Epidemiology, Pathogenesis, and Biomarkers of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy. J Clin Neurol. 2023 Jan;19(1):12-27. (SCI, 107/212, Clinical Neurology).

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*. (2022, Apr). Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy. Brain, 145;3010-3021. (SCI, 6/208, clnical neurology).

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. (2022, Jan). GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies. Neurology, 98(2):e199-e206.. (SCI, 12/208, clinical neurology)

Hsu SL, Chen YH, Chou CT, Chou YT, Tsai YS, Hsiao CT, Liao YC*, Lee YC*. (2021, Nov). Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype. Parkinsonism Relat Disord, 92:7-12. (SCI, 51/208, clinical neurology).

Liu YH, Guo YC, Lin LY, Tsai CP, Fuh JL, Wang YF, Chen SP, Wu HM, Yu KW, Lin KP, Wang SJ, Liao YC*, Lee YC*. (2021, Nov). Treatment response, risk of relapse and clinical characteristics of Taiwanese patients with neuromyelitis optica spectrum disorder. J Formos Med Assoc. 2022 Sep;121(9):1647-1656.

Tsai PC, Fuh JL, Yang CC, Chang A, Lien LM, Wang PN, Lai KL, Tsai YS, Lee YC*, Liao YC*. (2021, Nov). Clinical and genetic characterization of adult-onset leukoencephalopathy caused by CSF1R mutations. Ann Clin Transl Neurol., 8(11):2121-2131. (SCI, 59/208, clinical neurology).

Yi-Chu Liao, Yu-Chen Hu,* Chih-Ping Chung,Yen-Feng Wang, Yuh-Cherng Guo, Yu-Shuen Tsai, Yi-Chung Lee (2021, Mar). Intracerebral hemorrhage in CADASIL: prevalence, clinical and neuroimaging features and risk factors. Stroke, 52(3):985-993. (SCI, 16/204, Clinical Neurology).

Chung CP, Chen JW, Chang FC, Li WC, Lee YC, Chen LF*, Liao YC*. (2020, Jun). Cerebral Microbleed Burdens in Specific Brain Regions Are Associated With Disease Severity of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy. J Am Heart Assoc. 2020 Jul 7;9(13):e016233.. (SCI, 34/136, cardiac and cardiovascular diseases).

Lee YC, Chung CP, Chang MH, Wang SJ, Liao YC. (2020, Jan). NOTCH3 cysteine-altering variant is an important risk factor for stroke in the Taiwanese population. Neurology, 2020 Jan 7;94(1):e87-e96. (SCI, 10/199, clinical neurology).

Liao YC, Lee YC. (2019, Sep). Reply: A novel WARS mutation causes distal hereditary motor neuropathy in a Chinese family. Brain, 2019 Sep 1;142(9):e50. (SCI, 6/199, clinical neurology).

Hsu YH, Lin KP, Guo YC, Tsai YS, Liao YC*, Lee YC*. (2019, May). Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in Taiwan. Ann Clin Transl Neurol., 2019 May 27;6(6):1090-1101.

Lin YC, Lee YC, Hsu TY, Liao YC*, Soong BW*. (2019, May). Comparable progression of spinocerebellar ataxias between Caucasians and Chinese. Parkinsonism Relat Disord, 2019 May;62:156-162. (SCI, 37/199, clinical neurology).

Lee YC, Chung CP, Chao NC, Fuh JL, Chang FC, Soong BW, Liao YC (2018, Jul). Characterization of Heterozygous HTRA1 Mutations in Taiwanese Patients With Cerebral Small Vessel Disease. Stroke, 49(7):1593-1601. (SCI, 16/197, clinical neurology).