Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Yo Tsen Liu"'
Autor:
Yan-Ting Lu, Chung-Yao Hsu, Yo-Tsen Liu, Chung-Kin Chan, Yao-Chung Chuang, Chih-Hsiang Lin, Kai-Ping Chang, Chen-Jui Ho, Ching-Ching Ng, Kheng-Seang Lim, Meng-Han Tsai
Publikováno v:
Biomedical Journal, Vol 45, Iss 3, Pp 542-548 (2022)
Background: Periventricular nodular heterotopia (PVNH) is caused by abnormal neuronal migration, resulting in the neurons accumulate as nodules along the surface of the lateral ventricles. PVNH often cause epilepsy, psychomotor development or cogniti
Externí odkaz:
https://doaj.org/article/22ca7cdfa34d4817a703a5af7b78f1bf
Improving Executive Function and Dual-Task Cost in Parkinson Disease: A Randomized Controlled Trial.
Publikováno v:
Journal of Neurologic Physical Therapy; Oct2024, Vol. 48 Issue 4, p188-197, 10p
Autor:
Yo‐Tsen Liu, Yueh‐Jung Yen, Frans Ricardo, Yu Chang, Pei‐Hao Wu, Shing‐Jong Huang, Kon‐Ping Lin, Tsyr‐Yan Yu
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 10, Pp 1961-1970 (2019)
Abstract Objective Ala97Ser (A97S) is the major transthyretin (TTR) mutation in Taiwanese patients of familial amyloid polyneuropathy (FAP), characterized by a late‐onset but rapidly deteriorated neuropathy. Tafamidis can restore the stability of s
Externí odkaz:
https://doaj.org/article/7ca68388ed9c4c9599b91b584413d27f
Autor:
Hua‐Chuan Chao, Yi‐Chu Liao, Yo‐Tsen Liu, Yuh‐Cherng Guo, Fu‐Pang Chang, Yi‐Chung Lee, Kon‐Ping Lin
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 5, Pp 913-922 (2019)
Abstract Objective The clinical and genetic profiles of hereditary transthyretin amyloidosis (ATTR) in Chinese populations remain elusive. We aim to characterize the features of ATTR in a Taiwanese cohort of Han Chinese descent. Methods Seventy‐nin
Externí odkaz:
https://doaj.org/article/801a296b9e69416b84e888d92784b63f
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Transthyretin amyloidosis (ATTR amyloidosis) is a fatal systemic disease caused by amyloid deposits of misfolded transthyretin, leading to familial amyloid polyneuropathy and/or cardiomyopathy, or a rare oculoleptomeningeal amyloidosis. A good model
Externí odkaz:
https://doaj.org/article/49f484de64394bc5ae95880dad011bb3
Autor:
Yo-Tsen Liu, Yi-Chieh Chen, Shang-Yeong Kwan, Chien-Chen Chou, Hsiang-Yu Yu, Der-Jen Yen, Kwong-Kum Liao, Wei-Ta Chen, Yung-Yang Lin, Rou-Shayn Chen, Kang-Yang Jih, Shu-Fen Lu, Yu-Te Wu, Po-Shan Wang, Fu-Jung Hsiao
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Paroxysmal kinesigenic dyskinesia (PKD) is conventionally regarded as a movement disorder (MD) and characterized by episodic hyperkinesia by sudden movements. However, patients of PKD often have sensory aura and respond excellently to antiepileptic a
Externí odkaz:
https://doaj.org/article/e32a9c85c4744c668407e1f30f6ed904
Publikováno v:
PLoS ONE, Vol 13, Iss 2, p e0192866 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0187503.].
Externí odkaz:
https://doaj.org/article/2349c98bb1594a51bad1fdfdc4279be4
Autor:
Li-Hsin Chang, Nai-Fang Chi, Chun-Yu Chen, Yung-Shuan Lin, Shao-Lun Hsu, Jui-Yao Tsai, Hui-Chi Huang, Chun-Jen Lin, Chih-Ping Chung, Chien-Yi Tung, Chung-Jiuan Jeng, Yi-Chung Lee, Yo-Tsen Liu, I-Hui Lee
Publikováno v:
Cellular and Molecular Neurobiology.
Whole exome sequencing (WES) has been used to detect rare causative variants in neurological diseases. However, the efficacy of WES in genetic diagnosis of clinically heterogeneous familial stroke remains inconclusive. We prospectively searched for d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2badf3e39bb8d177c6051272f00b72
https://doi.org/10.1007/s10571-022-01315-3
https://doi.org/10.1007/s10571-022-01315-3
Publikováno v:
2022 14th Biomedical Engineering International Conference (BMEiCON).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c51f7f3164d0f191aa2ee1efcc60df0
https://doi.org/10.1109/bmeicon56653.2022.10012114
https://doi.org/10.1109/bmeicon56653.2022.10012114
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0187503 (2017)
The inositol 1,4,5-triphosphate (IP3) receptor type 1 gene (ITPR1) encodes the IP3 receptor type 1 (IP3R1), which modulates intracellular calcium homeostasis and signaling. Mutations in ITPR1 have been implicated in inherited cerebellar ataxias. The
Externí odkaz:
https://doaj.org/article/6383560f4a11444c90dac7e42e0ec8b4