1. Assessing the NOTCH2NLC GGC repeat expansion in Taiwanese patients with hereditary spastic paraplegia. (March 2022) Authors: Hsu, Shao-Lun; Jih, Kang-Yang; Lin, Kon-Ping; Liao, Yi-Chu; Lee, Yi-Chung Journal: Parkinsonism & related disorders Issue: Volume 96(2022) Page Start: 43 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Characterization of Heterozygous HTRA1 Mutations in Taiwanese Patients With Cerebral Small Vessel Disease. Issue 7 (July 2018) Authors: Lee, Yi-Chung; Chung, Chih-Ping; Chao, Nai-Chen; Fuh, Jong-Ling; Chang, Feng-Chi; Soong, Bing-Wing; Liao, Yi-Chu Journal: Stroke Issue: Volume 49:Issue 7(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan. (June 2021) Authors: Hsu, Shao-Lun; Hsueh, Hsueh-Wen; Chen, Shih-Ying; Chang, Yung-Yee; Tan, Shennie; Hong, Chien-Tai; Tsai, Yu-Shuen; Yu, Kai-Wei; Wu, Hsiu-Mei; Liao, Yi-Chu; Soong, Bing-Wen; Hu, Chaur-Jong; Lan, Min-Yu; Lee, Yi-Chung Journal: Parkinsonism & related disorders Issue: Volume 87(2021) Page Start: 87 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clinical and Molecular Characterization of PMP22 point mutations in Taiwanese patients with Inherited Neuropathy. Issue 1 (December 2017) Authors: Liao, Yi-Chu; Tsai, Pei-Chien; Lin, Thy-Sheng; Hsiao, Cheng-Tsung; Chao, Nai-Chen; Lin, Kon-Ping; Lee, Yi-Chung Journal: Scientific reports Issue: Volume 7:Issue 1(2017) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Gain of C-Ala enables AlaRS to target the L-shaped tRNAAla. Issue 4 (31st January 2022) Authors: Antika, Titi Rindi; Chrestella, Dea Jolie; Ivanesthi, Indira Rizqita; Rida, Gita Riswana Nawung; Chen, Kuan-Yu; Liu, Fu-Guo; Lee, Yi-Chung; Chen, Yu-Wei; Tseng, Yi-Kuan; Wang, Chien-Chia Journal: Nucleic acids research Issue: Volume 50:Issue 4(2022) Page Start: 2190 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic and Functional Analysis of Glycosyltransferase 8 Domain–Containing Protein 1 in Taiwanese Patients With Amyotrophic Lateral Sclerosis. (3rd December 2021) Authors: Tsai, Pei-Chien; Jih, Kang-Yang; Shen, Ting-Yi; Liu, Yi-Hong; Lin, Kon-Ping; Liao, Yi-Chu; Lee, Yi-Chung Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetic and Functional Analysis of Glycosyltransferase 8 Domain–Containing Protein 1 in Taiwanese Patients With Amyotrophic Lateral Sclerosis. (December 2021) Authors: Tsai, Pei-Chien; Jih, Kang-Yang; Shen, Ting-Yi; Liu, Yi-Hong; Lin, Kon-Ping; Liao, Yi-Chu; Lee, Yi-Chung Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies. (11th January 2022) Authors: Liao, Yi-Chu; Chang, Fu-Pang; Huang, Han-Wei; Chen, Ting-Bing; Chou, Ying-Tsen; Hsu, Shao-Lun; Jih, Kang-Yang; Liu, Yi-Hong; Hsiao, Cheng-Tsung; Fukukda, Hiromi; Mizuguchi, Takeshi; Lin, Kon-Ping; Lin, Chou-Ching K.; Matsumoto, Naomichi; Kennerson, Marina; Lee, Yi-Chung Journal: Neurology Issue: Volume 98:Number 2(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Incidental findings on brain magnetic resonance imaging: systematic review and meta-analysis. (17th August 2009) Authors: Morris, Zoe; Whiteley, William N; Longstreth, W T; Weber, Frank; Lee, Yi-Chung; Tsushima, Yoshito; Alphs, Hannah; Ladd, Susanne C; Warlow, Charles; Wardlaw, Joanna M; Al-Shahi Salman, Rustam Journal: BMJ Issue: Volume 339(2009) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype. (November 2021) Authors: Hsu, Shao-Lun; Chen, Ying-Hao; Chou, Cheng-Ta; Chou, Ying-Tsen; Tsai, Yu-Shuen; Hsiao, Cheng-Tsung; Liao, Yi-Chu; Lee, Yi-Chung Journal: Parkinsonism & related disorders Issue: Volume 92(2021) Page Start: 7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗