Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Tzu Jou Wang"'
Publikováno v:
Biomedical Journal, Vol 46, Iss 2, Pp 100524- (2023)
Background: The precise contribution of each chromosome gene or gene family in achieving male fertility is still the subject of debate. Most studies have examined male populations with heterogeneous causes of infertility, and have therefore reached c
Externí odkaz:
https://doaj.org/article/7a37b690fcfb402f8be193bbbd153905
Publikováno v:
Taiwan Journal of Ophthalmology, Vol 12, Iss 4, Pp 423-429 (2022)
PURPOSE: The purpose of this study was to identify gene mutation and phenotype correlations in a cohort of Taiwanese patients with Stickler syndrome. MATERIALS AND METHODS: Patients clinically diagnosed with Stickler syndrome or suspected Stickler sy
Externí odkaz:
https://doaj.org/article/103ccc097478414a9a0e185f6d98c784
Autor:
Hsiang-Yu Lin, Chung-Lin Lee, Chia-Ying Chang, Pao Chin Chiu, Yin-Hsiu Chien, Dau-Ming Niu, Fuu-Jen Tsai, Wuh-Liang Hwu, Shio Jean Lin, Ju-Li Lin, Mei-Chyn Chao, Tung-Ming Chang, Wen-Hui Tsai, Tzu-Jou Wang, Chih-Kuang Chuang, Shuan-Pei Lin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Mucopolysaccharidoses (MPSs) are a group of inherited metabolic diseases, which are characterized by the accumulation of glycosaminoglycans, and eventually lead to the progressive damage of various tissues and organs. Methods An e
Externí odkaz:
https://doaj.org/article/1a7cb82677974c78a14f127068c04131
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:
Tsu-Kung Lin, Kai-Jung Lin, Kai-Lieh Lin, Chia-Wei Liou, Shang-Der Chen, Yao-Chung Chuang, Pei-Wen Wang, Jiin-Haur Chuang, Tzu-Jou Wang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Parkinson's disease (PD) is a complex neurodegenerative disease with pathological hallmarks including progressive neuronal loss from the substantia nigra pars compacta and α-synuclein intraneuronal inclusions, known as Lewy bodies. Although the etio
Externí odkaz:
https://doaj.org/article/c8ffac486a2f4ab2ae251dd3f8af73a6
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
Publikováno v:
Pediatrics and Neonatology, Vol 51, Iss 6, Pp 326-329 (2010)
Cartilage-hair hypoplasia (MIM 250250) is an autosomal recessive disease with diverse clinical manifestations. The clinical phenotypes include variable degrees of bone and hair dysplasia, deficient cellular and/or humoral immunity, and a predispositi
Externí odkaz:
https://doaj.org/article/655e780ee5c04b0ebc536568b63847a7
Autor:
Yin-Hsiu Chien, Wen-Hui Tsai, Shio Jean Lin, Ju-Li Lin, Dau-Ming Niu, Chih-Kuang Chuang, Chung-Lin Lee, Wuh-Liang Hwu, Tzu-Jou Wang, Pao Chin Chiu, Fuu Jen Tsai, Shuan-Pei Lin, Hsiang-Yu Lin, Tung-Ming Chang, Mei-Chyn Chao, Chia-Ying Chang
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Background Mucopolysaccharidoses (MPSs) are a group of inherited metabolic diseases, which are characterized by the accumulation of glycosaminoglycans, and eventually lead to the progressive damage of various tissues and organs. Methods An epidemiolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28a58c649b7fadc0b767ab2d63fec1d0
https://pubmed.ncbi.nlm.nih.gov/33160388
https://pubmed.ncbi.nlm.nih.gov/33160388
Publikováno v:
Pediatrics and neonatology. 60(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::449f6ef01cb16e73f6855e565d20dad5
https://pubmed.ncbi.nlm.nih.gov/30982524
https://pubmed.ncbi.nlm.nih.gov/30982524
Autor:
Ni-Chung Lee, Chao Szu Wu, Hung-Bin Tsai, Shao Yin Chu, Yin-Hsiu Chien, Chih Hung Chen, Wang-Tso Lee, Tzu Jou Wang, Shio Jean Lin, Chao Ching Huang, Wen-Chin Weng, Kun Long Hung, Pi-Chuan Fan, Pei-Lin Lee, Han Chung Hsiue, Chih-Chao Yang, Wuh-Liang Hwu, Chien Jung Lu
Publikováno v:
Intensive Care Medicine. 41:1493-1495
Dear Editor, Mitochondrial DNA 3243A[G is the most common pathogenic mutation of the tRNA gene, accounting for 80 % of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) [1]. As a result of multi-organ involvement, patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7ddcda0f0881c43cf270100e8f59aba
https://doi.org/10.1007/s00134-015-3879-x
https://doi.org/10.1007/s00134-015-3879-x