得獎紀錄：

1. 2026年臺灣神經學學會壁報論文口頭報告優等
2. 2025年臺北市醫師公會青年杏林奬
3. 2025年臺北榮民總醫院住院醫師杏林獎第一名
4. 2025年吳舜⽂基⾦會李良雄教授論⽂獎
5. 2024年臺灣神經罕⾒疾病學會年會暨國際學術研討會，海報發表佳作
6. 2022年度臺北榮民總醫院最佳教學住院醫師
7. 2022年臺灣神經罕見疾病學會年會論文口頭報告金獎

媒體影音報導:

手腳末梢疼痛、皮膚現黑紫疹 竟是遺傳疾病惹禍（自由健康網 2025/4/23）

論文發表：

1. Fang SY , Jih KY , Chao YC, Sytwu HP , Shih YC, Liao YC, Lee YC. Clinical and electrophysiological features for differentiating MMN from hand-onset ALS. J Chin Med Assoc. 2026;89(6):437-444.
2. Sytwu HP, Jih KY, Tsai YS, Fang SY, Liao YC, Lee YC. FUS-associated ALS in Taiwan: genetic spectrum, clinical features, and a founder haplotype of p.H517D. J Neurol. 2026;273(7):387. 
3. Jih KY, Tsai YS, Fang SY, Hsu FC, Sytwu HP, Liao YC, Tsai PC, Lee YC. SOD1 mutations in Taiwanese ALS patients: Clinical characteristics, frequency, and a p.T138R founder effect. Amyotroph Lateral Scler Frontotemporal Degener. 2026;27(3-4):338-347.
4. Jih KY, Fang SY, Lee YC. Advances in ALS genetics and emerging precision therapies. J Formos Med Assoc. 2025;125(1):S48-S54.
5. Jih KY, Hsu TR, Fuh JL, Lee TH, Lin YS, Fang SY, Liao YC, Lee YC. Early presentation of spastic paraparesis in individuals carrying PSEN1 mutations: a clinical and genetic analysis. Alzheimers Res Ther. 2025 Apr 30;17(1):96.
6. Fang SY, Hsiao CT, Jih KY, et al. Investigating ITM2B-associated ataxia in a Taiwanese cerebellar ataxia cohort. Ann Clin Transl Neurol. 2025;12(1):158-168.
7. Jih KY, Fang SY, Tsai YS, Sytwu HP, Liao YC, Lee YC. TARDBP variants in Taiwanese ALS patients: Genetic spectrum, clinical features, and founder effects. J Neurol Sci. 2025;474:123531. 
8. Chen, SC, Chen YH, Fang SY, Hsu HT, Chang FP, Jih KY, Liao YC, Lee YC, Lai KL. Neuronal Intranuclear Inclusion Disease Mimicking Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Case Report. Acta Neurol Taiwan. 2025;34(4):239-244.
9. Fang SY, Tsai PC, Jih KY, Hsu FC, Liao YC, Yang CC, Lee YC. TBK1 p.Y153Qfs*9 variant may associate with young onset, rapidly progressive ALS through a haploinsufficiency mechanism. J Chin Med Assoc. 2024;87(10):920-926.
10. Fang SY, Chou YT, Hsu KC, et al. Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia. Ann Clin Transl Neurol. 2023;10(3):353-362. 
11. Juan CH, Fang SY, Chou CH, Tsai TY, Lin YT. Clinical characteristics of patients with pneumonia caused by Klebsiella pneumoniae in Taiwan and prevalence of antimicrobial-resistant and hypervirulent strains: a retrospective study. Antimicrob Resist Infect Control. 2020;9(1):4.