Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Yung‐Yee Chang"'
Publikováno v:
BMC Infectious Diseases, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract The neurological complications of influenza affect mainly the pediatric Asian population. In the category of influenza-associated encephalopathy, acute necrotizing encephalopathy (ANE) is a rapidly progressive and fulminant brain disorder as
Externí odkaz:
https://doaj.org/article/637b8c0620ce445fb86d119e765028c9
Autor:
Pin‐Shiuan Chen, Ying‐Fa Chen, Jian‐Ying Chiu, Meng‐Chen Wu, Chun‐Hwei Tai, Yung‐Yee Chang, Min‐Yu Lan, Ni‐Chung Lee, Chin‐Hsien Lin
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 6, Pp 1557-1566 (2024)
Abstract Objective IRF2BPL mutation has been associated with a rare neurodevelopmental disorder with abnormal movements, including dystonia. However, the role of IRF2BPL in dystonia remains elusive. We aimed to investigate IRF2BPL mutations in a Taiw
Externí odkaz:
https://doaj.org/article/850d1fcf49384b5eb997d8255da6a682
Autor:
Meng-Chen Wu, Yung-Yee Chang, Ying-Fa Chen, Min-Yu Lan, Pei-Lung Chen, Chun-Hwei Tai, Chin-Hsien Lin
Publikováno v:
Journal of the Formosan Medical Association, Vol 121, Iss 1, Pp 375-380 (2022)
Background/purpose: A heterozygous three-nucleotide (GAG) in-frame deletion in the TOR1A gene causes the rare disease, dystonia (DYT1), which typically presents as focal limb dystonia during adolescence, then spreads to other limbs. This study invest
Externí odkaz:
https://doaj.org/article/bb487adbcfb942b298acecac7b3ff7ea
Autor:
Mu‐Hui Fu, Chih‐Cheng Huang, Kay L. H. Wu, Ying‐Fa Chen, Yu‐Chih Kung, Cheng‐Chang Lee, Jia‐Shou Liu, Min‐Yu Lan, Yung‐Yee Chang
Publikováno v:
Brain and Behavior, Vol 13, Iss 2, Pp n/a-n/a (2023)
Abstract Objectives The classic triad of idiopathic normal pressure hydrocephalus (NPH) encompass gait disturbance, cognitive impairment, and urinary incontinence. These symptoms overlap with parkinsonism but with distinct treatment. Lacking applicab
Externí odkaz:
https://doaj.org/article/4ca1dde6a62647f5b2f363ad6db089d6
Autor:
Yuan-Pin Lin, Hsing-Yi Liang, Yueh-Sheng Chen, Cheng-Hsien Lu, Yih-Ru Wu, Yung-Yee Chang, Wei-Che Lin
Publikováno v:
Journal of NeuroEngineering and Rehabilitation, Vol 18, Iss 1, Pp 1-12 (2021)
Abstract Background Patients with Parkinson’s disease (PD) can develop impulse control disorders (ICDs) while undergoing a pharmacological treatment for motor control dysfunctions with a dopamine agonist (DA). Conventional clinical interviews or qu
Externí odkaz:
https://doaj.org/article/3a24dac9252a492f9fbad296250607a6
Autor:
Min-Yu Lan, Chin-Song Lu, Shey-Lin Wu, Ying-Fa Chen, Yueh-Feng Sung, Min-Chien Tu, Yung-Yee Chang
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders clinically characterized by progressive lower-limb spasticity. Cerebellar ataxia commonly co-occurs with complicated HSPs. HSP with concurrent cerebellar a
Externí odkaz:
https://doaj.org/article/887b8652f6ba48ceb6c8f36cf95e9b08
Autor:
Yu Lee, Yu-Jie Chiou, Chi-Fa Hung, Yung-Yee Chang, Ying-Fa Chen, Tsu-Kung Lin, Liang-Jen Wang
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Parkinson's disease (PD) is an incapacitating neurodegenerative disease. Patients with PD and their caregivers may have interactive effects on each other’s psychological well-being. This study aimed to assess the dyadic dynamics of resilie
Externí odkaz:
https://doaj.org/article/03f6b1bc939c4a298ee8b56d6758265d
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background Primary familial brain calcification (PFBC) is a rare inherited disease characterized by multiple calcified foci in the brain parenchyma. MYORG is the first gene found to be associated with autosomal recessive PFBC. The precise pa
Externí odkaz:
https://doaj.org/article/09bdef2db0574ec9b0304d5b5b639241
Publikováno v:
BMC Neurology, Vol 17, Iss 1, Pp 1-6 (2017)
Abstract Background Vacuolar protein sorting 35 (VPS35) was recently reported to be a genetic cause for late-onset autosomal dominant Parkinson’s disease (PD). However, VPS35 mutations are rarely reported in Asian populations. Herein, we report the
Externí odkaz:
https://doaj.org/article/88fca56160b1422e85c2aff622389fac
Autor:
Tsu-Kung Lin, Yung-Yee Chang, Hung-Yu Lin, Chia-Wei Liou, Pei-Wen Wang, Jiin-Haur Chuang, Shang-Der Chen, Yao-Chung Chuang, Sheng-Teng Huang, Te-Yao Hsu, Cheng-Huei Peng, Min-Yu Lan
Publikováno v:
PLoS ONE, Vol 14, Iss 10, p e0224173 (2019)
Several inherited human diseases have been linked to mitochondrial aminoacyl-tRNA synthetases (mtARSs). Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) is a leukodystrophy caused by mutations in the DARS2 g
Externí odkaz:
https://doaj.org/article/273559d6f21f4cb3a0459a56e53033f9