Zobrazeno 1 - 10
of 224
pro vyhledávání: '"Yi‐Chung Lee"'
Autor:
Kon-Ping Lin, Chih-Chao Yang, Yi-Chung Lee, Ming-Jen Lee, John Vest, Marianne T. Sweetser, Matthew T. White, Prajakta Badri, Sung-Tsang Hsieh, Chi-Chao Chao
Publikováno v:
Journal of the Formosan Medical Association, Vol 123, Iss 9, Pp 975-984 (2024)
Background: To examine the efficacy and safety of patisiran, an RNA interference therapeutic, in patients from Taiwan with hereditary transthyretin-mediated (hATTR) amyloidosis with polyneuropathy. Methods: The APOLLO phase 3 trial included patients
Externí odkaz:
https://doaj.org/article/dab5699cac1045209b1a2938728fe680
Autor:
Hsiang-Ting Hsu, Hui-Chen Cheng, Tsung-Wei Hou, Yi-Shiang Tzeng, Jong-Ling Fuh, Shih-Pin Chen, Wei-Ta Chen, Wei-Ju Lee, Yen-Wei Pai, Yi-Chung Lee, Jiing-Feng Lirng, Shuu-Jiun Wang, Yen-Feng Wang
Publikováno v:
The Journal of Headache and Pain, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background There have been limited data on idiopathic intracranial hypertension (IIH) in Asians and there remain uncertainties whether a cerebrospinal fluid (CSF) pressure of 250 mm CSF is an optimum diagnostic cutoff. The aims of the presen
Externí odkaz:
https://doaj.org/article/0c0ab929731e4aa7b85e2dc389dc86dd
Autor:
Cheng‐Tsung Hsiao, Tzu‐Yun Tsai, Ting‐Yi Shen, Yu‐Shuen Tsai, Yi‐Chu Liao, Yi‐Chung Lee, Pei‐Chien Tsai
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 7, Pp 1909-1920 (2024)
Abstract Objective TFG mutations have previously been implicated in autosomal recessive hereditary spastic paraplegia (HSP), also known as SPG57. This study aimed to investigate the clinical and molecular features of TFG mutations in a Taiwanese HSP
Externí odkaz:
https://doaj.org/article/283eded396fc435b9379fe01b6dea680
Autor:
Yu-Ju Liu, Chia-Wei Lee, Yi-Chu Liao, Joseph Jen-Tse Huang, Hung-Chih Kuo, Kang-Yang Jih, Yi-Chung Lee, Yijuang Chern
Publikováno v:
Neurobiology of Disease, Vol 202, Iss , Pp 106715- (2024)
Hypermetabolism is a prominent characteristic of ALS patients. Aberrant activation of AMPK, an energy sensor regulated by adiponectin, is known to cause TDP-43 mislocalization, an early event in ALS pathogenesis. This study aims to evaluate the assoc
Externí odkaz:
https://doaj.org/article/c59dd19c6624414084bc7bcefe65906f
Autor:
Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 5, Pp 1091-1114 (2024)
Abstract PAR3/INSC/LGN form an evolutionarily conserved complex required for asymmetric cell division in the developing brain, but its post-developmental function and disease relevance in the peripheral nervous system (PNS) remains unknown. We mapped
Externí odkaz:
https://doaj.org/article/5359f09eb23c4e93a0c5ca897d7a0804
Publikováno v:
Journal of Stroke, Vol 26, Iss 1, Pp 112-115 (2024)
Externí odkaz:
https://doaj.org/article/4210a7b8e62642059e5c3ff9bc5cc374
Autor:
Ying‐Tsen Chou, Shao‐Lun Hsu, Yu‐Shuen Tsai, Yi‐Jiun Lu, Kai‐Wei Yu, Hsiu‐Mei Wu, Yi‐Chu Liao, Yi‐Chung Lee
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 9, Pp 1603-1612 (2023)
Abstract Objective Hereditary spastic paraplegias (HSPs) are a group of inherited neurodegenerative disorders characterized by slowly progressive lower limb spasticity and weakness. HSP type 54 (SPG54) is autosomal recessively inherited and caused by
Externí odkaz:
https://doaj.org/article/54fb5979efc84d9ba071e5980d4e8893
Autor:
Satoshi Saito, Soichiro Abe, Kunihiro Nishimura, Toshiki Mizuno, Osamu Onodera, Sung-Chun Tang, Yi-Chung Lee, Jay Chol Choi, Masafumi Ihara
Publikováno v:
Cerebral Circulation - Cognition and Behavior, Vol 6, Iss , Pp 100336- (2024)
Introduction: Recent advancements in genomic research have revealed that 9 individuals per 1,000 population in East Asia and 3.4 individuals per 1,000 population worldwide carry cysteine-altering NOTCH3 variants in the epidermal growth factor-like re
Externí odkaz:
https://doaj.org/article/8ecdc396b8eb4fec89344800d91fa4ed
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Clopidogrel is the most-widely used platelet P2Y12-inhibitor for secondary-prevention of ischemic stroke. Platelet P2Y12 reactivity before and after inhibitors can be measured with blood sampling by commercialized system. We aimed to evaluat
Externí odkaz:
https://doaj.org/article/41fc3eb655284bf797517608c995d9ac
Autor:
Shih‐Yu Fang, Ying‐Tsen Chou, Kuo‐Chou Hsu, Shao‐Lun Hsu, Kai‐Wei Yu, Yu‐Shuen Tsai, Yi‐Chu Liao, Pei‐Chien Tsai, Yi‐Chung Lee
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 3, Pp 353-362 (2023)
Abstract Objective NIPA1 mutations have been implicated in hereditary spastic paraplegia (HSP) as the cause of spastic paraplegia type 6 (SPG6). The aim of this study was to investigate the clinical and genetic features of SPG6 in a Taiwanese HSP coh
Externí odkaz:
https://doaj.org/article/512e80aa1e98488187e6baa056a3fd06