Zobrazeno 1 - 10
of 146
pro vyhledávání: '"Min‐Yu Lan"'
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:
Min-Yu Lan, Tsu-Kung Lin, Baiba Lace, Algirdas Utkus, Birute Burnyte, Kristina Grigalioniene, Yu-Han Lin, Inna Inashkina, Chia-Wei Liou
Publikováno v:
Cells, Vol 13, Iss 8, p 694 (2024)
Variants of mitochondrial DNA (mtDNA) have been identified as risk factors for the development of Parkinson’s disease (PD). However, the underlying pathogenetic mechanisms remain unclear. Cybrid models carrying various genotypes of mtDNA variants w
Externí odkaz:
https://doaj.org/article/cc2baf2bc8854905bc64071550759ef6
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:
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
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
Autor:
Kai-Jung Lin, Shang-Der Chen, Kai-Lieh Lin, Chia-Wei Liou, Min-Yu Lan, Yao-Chung Chuang, Pei-Wen Wang, Jong-Jer Lee, Feng-Sheng Wang, Hung-Yu Lin, Tsu-Kung Lin
Publikováno v:
Cells, Vol 11, Iss 23, p 3829 (2022)
Parkinson disease (PD) is the second-most common neurodegenerative disease. The characteristic pathology of progressive dopaminergic neuronal loss in people with PD is associated with iron accumulation and is suggested to be driven in part by the nov
Externí odkaz:
https://doaj.org/article/e4d04c2af58b4fbdaec38e3da9af748b
Autor:
Tsu-Kung Lin, Kai-Jung Lin, Hung-Yu Lin, Kai-Lieh Lin, Min-Yu Lan, Pei-Wen Wang, Tzu-Jou Wang, Feng-Sheng Wang, Po-Chin Tsai, Chia-Wei Liou, Jiin-Haur Chuang
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
Parkinson disease (PD) is the second most common neurodegenerative disease without known disease modification therapy to slow down disease progression. This disease has pathological features of Lewy bodies with α-synuclein aggregation being the majo
Externí odkaz:
https://doaj.org/article/c5cc7a3f60464186a247b112e32c9dd4
Autor:
Kai-Jung Lin, Tzu-Jou Wang, Shang-Der Chen, Kai-Lieh Lin, Chia-Wei Liou, Min-Yu Lan, Yao-Chung Chuang, Jiin-Haur Chuang, Pei-Wen Wang, Jong-Jer Lee, Feng-Sheng Wang, Hung-Yu Lin, Tsu-Kung Lin
Publikováno v:
Antioxidants, Vol 10, Iss 12, p 1935 (2021)
Parkinson’s disease (PD) is the second most common neurodegenerative disease after Alzheimer’s disease affecting more than 1% of the population over 65 years old. The etiology of the disease is unknown and there are only symptomatic managements a
Externí odkaz:
https://doaj.org/article/9cffad36f89c4cafbadb824f2c1e9cec