Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Han Yun Hsiao"'
Publikováno v:
American Journal of Physical Medicine & Rehabilitation; Apr2024, Vol. 103 Issue 4, p275-283, 9p
Publikováno v:
European Journal of Physical and Rehabilitation Medicine. 56
Background Most types of robot-assisted training (RT) have been used in Cerebral Palsy (CP) patients only focus on proximal upper extremity. Few of study investigated the effect of distal upper extremity training. Case report Pediatric CP patients (N
Autor:
Yi-Hua Hsu, Chiao-Chi Chen, Yu-Chen Chen, Chen Chang, Hui-Mei Chen, Hung-Chih Kuo, Feng-Lan Chiu, Han-Yun Hsiao, Yijuang Chern, Chien-Hsiang Huang
Publikováno v:
Annals of Neurology. 78:178-192
Objective Huntington disease (HD) is an inherited neurodegenerative disease caused by the mutant huntingtin gene (mHTT), which harbors expanded CAG repeats. We previously reported that the brain vessel density is higher in mice and patients with HD t
Autor:
Han-Yun Hsiao, Hui-Mei Chen, Yijuang Chern, Chien-Yuan Lin, Chiao-Chi Chen, Chen Chang, Tsai-Hui Yang, Yu-Chen Chen, Yi-Hua Hsu, Ming-Huang Lin
Publikováno v:
Experimental Neurology. 250:20-30
Cerebral microvascular aberrations have recently become recognized as a source of pathologies in neurodegenerative disorders, but this concept has not been fully examined with respect to Huntington's disease (HD). A novel in vivo technique, three-dim
Publikováno v:
Human Molecular Genetics. 22:1826-1842
Huntington's disease (HD) is an autosomal disease caused by a CAG repeat expansion in the huntingtin (HTT) gene. The resultant mutant HTT protein (mHTT) forms aggregates in various types of cells, including neurons and glial cells and preferentially
Autor:
Huey Min Yeh, Yi Hsiang Lin, Chung-Huei Hsu, Hung Jung Wang, Ching Huei Kung, Han Yun Hsiao, Pen Yuan Liao, Chun-Yao Huang, Ting-Kai Leung, Yu Ching Ting, Chi-Ming Lee
Publikováno v:
Journal of Experimental & Clinical Medicine. 4:275-279
Objective This study was to investigate the usefulness and limitations of cardiac magnetic resonance imaging (MRI). We compared echocardiography (ECHO) and perfusion scans to evaluate: left ventricular wall scar formation of the myocardium; hypokines
Autor:
Yow-Sien Lin, Ting Chien, Han-Yun Hsiao, Kai-Hsiang Chen, Yijuang Chern, Jun-Tasi Lin, Ching-Yu Chuang, Chiung-Mei Chen, Feng-Lan Chiu, Hung-Chih Kuo
Publikováno v:
Human molecular genetics. 24(21)
Huntington's disease (HD) is an autosomal-dominant degenerative disease caused by a cytosine-adenine-guanine trinucleotide expansion in the Huntingtin (htt) gene. The most vulnerable brain areas to mutant HTT-evoked toxicity are the striatum and cort
Publikováno v:
Glia. 55:214-223
Astrocytes, the most abundant glia in the central nervous system (CNS), produce a large amount of prostaglandin E(2) (PGE(2)) in response to proinflammatory mediators after CNS injury. However, it is unclear whether PGE(2) has a regulatory role in as
Publikováno v:
Current Drug Target -Inflammation & Allergy. 4:335-340
Many brain disorders such as Parkinson's disease, Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Huntington, stroke, head trauma, and infection, are associated with inflammation that is involved in neuropathologenesis and hyperalgesis. Mic
Autor:
Yih-Ru Wu, Hui-Mei Chen, Han-Yun Hsiao, Chiung-Mei Chen, Feng-Lan Chiu, Yu-Chen Chen, Hung-Chih Kuo, Yijuang Chern
Publikováno v:
Human molecular genetics. 23(16)
Neuroinflammation is a common feature of many neurodegenerative diseases, including Huntington's disease (HD). HD is an autosomal dominant genetic disease caused by an expanded CAG repeat in exon 1 of the huntingtin (HTT) gene. Previous studies demon