Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Xiang-xue ZHOU"'
Autor:
Xiang‐xue Zhou, Xun‐hua Li, Ding‐bang Chen, Chao Wu, Li Feng, Hao‐lin Qin, Xiao‐Yong Pu, Xiu‐ling Liang
Publikováno v:
Brain and Behavior, Vol 9, Iss 12, Pp n/a-n/a (2019)
Abstract Objective To evaluate different injury factors and pathological characteristics of the brain at different disease stages in toxic milk (TX) mice, an animal model of Wilson's disease (WD). Methods Thirty TX mice (10 each at 3, 6 and 12 months
Externí odkaz:
https://doaj.org/article/934656f1bb3b48708226b1291c85877e
Autor:
Ying-yin LIANG, Gui-dian LI, Rong-xing HE, Wei-wei QI, Xue XU, Xiang-xue ZHOU, Rong-lan1 ZHU, Lu YAO, Cheng ZHANG
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 18, Iss 7, Pp 501-505 (2018)
Objective To summarize the characteristics of fatty infiltration and edema of muscle MRI in Duchenne muscular dystrophy (DMD) patients. Methods A total of 70 DMD patients underwent Clinical Functional Scale and muscle MRI of the pelvic (gluteus maxim
Externí odkaz:
https://doaj.org/article/edc428847eab4ca8b871a09e63aa2a3b
Objective: To evaluate the changes of extrapyramidal network in Wilson disease (WD) patients after 5 years of copper excluding treatment using diffusion tensor imaging (DTI). Methods: 50 patients with WD, including 41 with cerebral type and 9 with he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::397209c1ec9b8010764457a06254c967
https://doi.org/10.21203/rs.3.rs-1190627/v1
https://doi.org/10.21203/rs.3.rs-1190627/v1
Publikováno v:
World Journal of Clinical Cases
BACKGROUND Mitochondrial diseases are a heterogenous group of multisystemic disorders caused by genetic mutations affecting mitochondrial oxidation function. Brain involvement is commonly found in most cases but rarely as the unique clinical manifest
Autor:
Guidian Li, Xue Xu, Cheng Zhang, Yingyin Liang, Ronglan Zhu, Songlin Chen, Xiang-xue Zhou, Rongxing He, Yingming Chen
Publikováno v:
Biomedical Reports. 7:193-196
The objective of the present study was to characterize the muscle magnetic resonance imaging (MRI) features of a 1-year-old girl with merosin-deficient congenital muscular dystrophy type 1A (MDC1A). Beginning as an infant, this patient exhibited seve
Autor:
Xiang-Xue Zhou1 1397880617@qq.com, Hao-Lin Qin2, Xun-Hua Li3, Hai-Wei Huang3, Ying-Ying Liang1, Xiu-Ling Liang3, Xiao-Yong Pu4
Publikováno v:
Neurology India. Jul/Aug2014, Vol. 62 Issue 4, p362-366. 5p.
Autor:
Yu-Kun, Song, Xin-Bei, Li, Xiao-Long, Huang, Jing, Zhao, Xiang-Xue, Zhou, Yu-Liang, Wang, Xu, Yan, Jing-Yan, Wang, Jian-Ping, Chu
Publikováno v:
Journal of magnetic resonance imaging : JMRI. 48(2)
Previous studies have indicated that neurite orientation dispersion and density imaging (NODDI) could be used as a biomarker for detecting microstructural changes of brain.To quantitatively evaluate the changes in basal ganglia (BG) and thalamus in W
Autor:
Dingbang Chen, Li Feng, Chao Wu, Jiwei Zhang, Xiang-xue Zhou, Xiu-Ling Liang, Huajing You, Zhong Pei, Xun-hua Li
Publikováno v:
CNS neurosciencetherapeutics. 23(4)
AIMS: To detect specific oculomotor deficits in preclinical stage of spinocerebellar ataxia type 3 (SCA3) and evaluate whether these abnormalities prove useful as potential biomarkers of disease progression. METHODS: A Chinese cohort of 56 patients w
Autor:
Li Feng, Xiang-xue Zhou, Haiman Hou, Chao Wu, Zhong Pei, Xiu-Ling Liang, Jun-Xiu Liu, Xiao-Pu Lin, Yinyin Liang, Ji-Wei Zhang, Xun-hua Li, Dingbang Chen
Publikováno v:
Therapeutic Advances in Neurological Disorders, Vol 9 (2016)
Objectives: There are limited pharmacological treatments for patients with neurological Wilson’s disease (WD) and a history of copper-chelating treatment failure. Methods: We retrospectively evaluated the clinical records of 38 patients with WD who
Autor:
Hao-Lin Qin, Xiang-xue Zhou, Xiu-Ling Liang, Gui-dian Li, Xiao-Yong Pu, Ying-Ying Liang, Haiwei Huang, Xun-hua Li
Publikováno v:
Journal of the neurological sciences. 362
Objective To evaluate damage to the extracorticospinal tract in Wilson disease (WD) patients using diffusion tensor imaging (DTI). Methods 70 patients with WD, including 50 with cerebral type and 20 with hepatic type, and 20 age-matched healthy contr