Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Min-ting Lin"'
Autor:
Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Fu-ze Zheng, Liang-liang Qiu, Zhi-xian Ye, Hai-zhu Chen, Min-ting Lin, Ning Wang, Zhi-qiang Wang
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-18 (2023)
Abstract Background Limb-girdle muscular dystrophies (LGMDs) are a group of heterogeneous inherited diseases predominantly characterized by limb-girdle muscle weakness and dystrophic changes on histological analysis. The frequency of LGMD subtypes va
Externí odkaz:
https://doaj.org/article/80189a10ec2d46fb8dda201e21e194aa
Autor:
Feng Lin, Kang Yang, Min‐ting Lin, Fu‐ze Zheng, Long Chen, Yuan‐liang Ding, Zhi‐xian Ye, Xin Lin, Ning Wang, Zhi‐qiang Wang
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 3, Pp 426-439 (2023)
Abstract Objective Oculopharyngeal muscular dystrophy (OPMD) is a late‐onset inherited neuromuscular disorder, with progressive ptosis and dysphagia as common manifestations. To date, OPMD has rarely been reported among East Asians. The present stu
Externí odkaz:
https://doaj.org/article/b8c0cd27b3f74d078e647da2b7a48d2d
Autor:
Miao Zhao, Hui-Zhen Su, Yi-Heng Zeng, Yuan Sun, Xin-Xin Guo, Yun-Lu Li, Chong Wang, Zhi-Yuan Zhao, Xue-Jing Huang, Kai-Jun Lin, Zi-Ling Ye, Bi-Wei Lin, Shunyan Hong, Jitan Zheng, Yao-Bin Liu, Xiang-Ping Yao, Dehao Yang, Ying-Qian Lu, Hai-Zhu Chen, Erwei Zuo, Guang Yang, Hong-Tao Wang, Chen-Wei Huang, Xiao-Hong Lin, Zhidong Cen, Lu-Lu Lai, Yan-Ke Zhang, Xi Li, Tianmin Lai, Jingjing Lin, Dan-Dan Zuo, Min-Ting Lin, Chia-Wei Liou, Qing-Xia Kong, Chuan-Zhu Yan, Zhi-Qi Xiong, Ning Wang, Wei Luo, Cui-Ping Zhao, Xuewen Cheng, Wan-Jin Chen
Publikováno v:
Cell Discovery, Vol 8, Iss 1, Pp 1-17 (2022)
Abstract Brain calcification is a critical aging-associated pathology and can cause multifaceted neurological symptoms. Cerebral phosphate homeostasis dysregulation, blood-brain barrier defects, and immune dysregulation have been implicated as major
Externí odkaz:
https://doaj.org/article/9415229f27c04eb299808dca7e144e8f
Publikováno v:
International Journal of Health Policy and Management, Vol 11, Iss 8, Pp 1307-1315 (2022)
Background With the promising outcomes of the pre-ESRD (end-stage renal disease) pay-for-performance (P4P) program, the National Health Insurance Administration (NHIA) of Taiwan launched a P4P program for patients with early chronic kidney disease (C
Externí odkaz:
https://doaj.org/article/3f9df8b37275487e99df3fba29128956
Autor:
Liang-Liang Qiu, Xiao-Dan Lin, Guo-Rong Xu, Li-Li Wang, Zhi-Xian Ye, Feng Lin, Hai-Zhu Chen, Min-Ting Lin, Nai-Qing Cai, Ming Jin, Liu-Qing Xu, Wei Hu, Ning Wang, Zhi-Qiang Wang, Li-Shao Guo
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 22, Pp 2753-2755 (2021)
Externí odkaz:
https://doaj.org/article/eecb6fd1948e4082a8be5b5932908fe6
Autor:
Qi-Fu Guo, Zhi-Xian Ye, Liang-Liang Qiu, Xin Lin, Jia-He Lai, Min-Ting Lin, Zhi-Qiang Wang, Ning Wang, Feng Lin, Jing Ni
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 5, Pp 622-624 (2021)
Externí odkaz:
https://doaj.org/article/b52215d3d64744cf8bbdb87d69380065
Autor:
Hai-Zhu Chen, Ming Jin, Nai-Qing Cai, Xiao-Dan Lin, Xin-Yi Liu, Liu-Qing Xu, Min-Ting Lin, Feng Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu, Yi Cui
Publikováno v:
Chinese Medical Journal, Vol 132, Iss 13, Pp 1615-1618 (2019)
Externí odkaz:
https://doaj.org/article/2fff0e1a423c42e1902353678b37ef51
Autor:
Jin-Shan Yang, Hao-Ling Xu, Ping-Ping Chen, Arif Sikandar, Mei-Zhen Qian, Hui-Xia Lin, Min-Ting Lin, Wan-Jin Chen, Ning Wang, Hua Wu, Shi-Rui Gan
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Spinocerebellar ataxia type 3 (SCA3) is an inherited form of ataxia that leads to progressive neurodegeneration. Fatigue is a common non-motor symptom in SCA3 and other neurodegenerative diseases, such as Parkinson's disease (PD) and amyo
Externí odkaz:
https://doaj.org/article/cd5a74f912dd44feb92786838e3a0484
Autor:
Guo-rong Xu, Wei Hu, Ling-Ling Zhan, Chong Wang, Liu-Qing Xu, Min-Ting Lin, Wan-Jin Chen, Ning Wang, Qi-Jie Zhang
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Amyotrophic lateral sclerosis (ALS) is a devastating motor neuron disease characterized by substantial clinical and genetic heterogeneity. Thus far, only a few TARDBP-ALS families have been reported in China, and no mutation analy
Externí odkaz:
https://doaj.org/article/8bbc57cb79074505866eef6165591f24
Autor:
Xiao-Dan Lin, Jun-Jie He, Feng Lin, Hai-Zhu Chen, Liu-Qing Xu, Wei Hu, Nai-Qing Cai, Min-Ting Lin, Ning Wang, Zhi-Qiang Wang, Guo-Rong Xu
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 18, Pp 2164-2171 (2018)
Background: Facioscapulohumeral muscular dystrophy (FSHD) is characterized by asymmetric muscular deficit of facial, shoulder-girdle muscles, and descending to lower limb muscles, but it exists in several extramuscular manifestations or overlapping s
Externí odkaz:
https://doaj.org/article/e16c5af090ef4ddcb0ee68da2b7a287f