Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yue-Huan Zuo"'
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 19, Iss 6, Pp 405-410 (2019)
Objective To investigate the clinical and neuropathological features of N-hexane toxic peripheral neuropathy which was misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Methods and Results Two patients presented with s
Externí odkaz:
https://doaj.org/article/2260b16206b449b2afa94ee3be6868f0
Autor:
Hui-Ting Lin, Xiao Liu, Wei Zhang, Jing Liu, Yue-Huan Zuo, Jiang-Xi Xiao, Ying Zhu, Yun Yuan, Zhao-Xia Wang
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 12, Pp 1472-1479 (2018)
Background: LMNA-related muscular dystrophy can manifest in a wide variety of disorders, including Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle muscular dystrophy (LGMD), and LMNA-associated congenital muscular dystrophy (L-CMD). Muscle magn
Externí odkaz:
https://doaj.org/article/39971d612d9146178be702486c978e5a
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 9, Pp 1049-1054 (2017)
Background: X-linked Charcot-Marie-Tooth type 1 (CMT1X) disease is one of the most common forms of inherited neuropathy caused by mutations in the gap junction beta-1 protein (GJB1) gene (also known as connexin 32). This study presented the clinical
Externí odkaz:
https://doaj.org/article/1b7d00fef45b41b09d7702f948cbd30e
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 16, Iss 10, Pp 689-695 (2016)
Objective To investigate the clinical manifestations and auxiliary examination features of necrotizing autoimmune myopathy (NAM). Methods According to the inclusion criteria from European Neuromuscular Center (ENMC) International Workshop on idiopath
Externí odkaz:
https://doaj.org/article/b4a4b2db5e654e60b0c2b52682282065
Autor:
Meng Yu, Zhe Zhang, Qing-Qing Wang, Jing Liu, Yue-Huan Zuo, Lei Yu, Jiang-Xi Xiao, Wei Zhang, Yun Yuan, Zhao-Xia Wang
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 12, Pp 1419-1424 (2016)
Background: Kearns-Sayre syndrome (KSS) is a mitochondrial DNA (mtDNA) deletion disorder characterized by a triad of onset before 20 years of age, ophthalmoplegia, and pigmentary retinopathy. The heart and central nervous system are commonly involved
Externí odkaz:
https://doaj.org/article/1f425eb9079c4ff28df1ea3bc09c0c3d
Autor:
Qian, Gao, Qing, Peng, Jing, Chen, Wei, Zhang, Zhao-xia, Wang, Yun, Yuan, Yue-huan, Zuo, Jing, Liu
Publikováno v:
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 47(5)
To evaluate the endothelial functions and autoregulation capacity of cerebral blood flow in patients with Fabry disease.Brachial artery vasodilation was assessed in 8 patients with Fabry disease and 14 healthy controls by means of flow-mediated dilat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::874b9fdd4e4032412d5fd82376d1f459
https://pubmed.ncbi.nlm.nih.gov/26474618
https://pubmed.ncbi.nlm.nih.gov/26474618