Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Xuguang, Gao"'
Publikováno v:
BMC Musculoskeletal Disorders, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background The underlying mechanism of muscle atrophy in sarcopenia is still not fully understood; branched chain aminotransferase 1(BCAT1) isocitrate dehydrogenase-1 encodes an evolutionarily conserved cytoplasmic aminotransferase for gluta
Externí odkaz:
https://doaj.org/article/ea79d233fb1b4ce5a551a7540ac5a17a
Features of hyperintense white matter lesions and clinical relevance in systemic lupus erythematosus
Autor:
Qian Guo, Yang He, Xia Liu, Xuguang Gao, Jing Xu, Xue Li, Yue Sun, Yajuan Xiang, Ru Li, Zhanguo Li, Lishao Guo
Publikováno v:
Chinese Medical Journal, Vol 135, Iss 8, Pp 962-970 (2022)
Abstract. Background:. Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease characterized by complex and various clinical manifestations. The study aimed to analyze clinical features and cerebral magnetic resonance imaging (MRI) cha
Externí odkaz:
https://doaj.org/article/3144e6346bfe4b6cb73aa3e749ea390f
Publikováno v:
Italian Journal of Pediatrics, Vol 47, Iss 1, Pp 1-9 (2021)
Abstract Purpose This study aimed to provide a summary of the measures to assess narcoleptic symptoms or complications in pediatric narcolepsy patients. Methods We searched in the National Center for Biotechnology Information (NCBI) for measures of n
Externí odkaz:
https://doaj.org/article/b74e42a447514e52bd2d7ac525300445
Publikováno v:
Particuology. 83:50-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c9eab647e6c0ee34367077da7061531
https://doi.org/10.1016/j.partic.2023.02.006
https://doi.org/10.1016/j.partic.2023.02.006
Autor:
Jing Shi, Mingqing Wei, Jingnian Ni, Feng Sun, Li Sun, Junfu Wang, Tao Yu, Kai Wang, Peiyuan Lv, Yunfu Wang, Yulian Zhang, Xuguang Gao, Xuanzhao Gao, Benyan Luo, Shanping Mao, Baorong Zhang, Xiangyang Ren, Fengchun Yu, Wenli Hu, Ping Yin, Nanjin Wu, Xianfeng Liu, Qi Bi, Yongyan Wang, Jinzhou Tian, The CHASE Study Group
Publikováno v:
Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-10 (2020)
Abstract Background and purpose Tianzhi granule (TZ) is usually used for patients with vascular dementia (VaD) in China. The aim was to assess the effect of TZ by a randomized clinical trial (RCT). Methods A 24-week RCT was conducted in 16 centres. P
Externí odkaz:
https://doaj.org/article/25d07f83120b4bc49013d8fad6390123
Publikováno v:
Frontiers in Aging Neuroscience, Vol 13 (2021)
Background: Cerebral small vessel disease (cSVD) and neurodegeneration are the two main causes of dementia and are considered distinct pathological processes, while studies have shown overlaps and interactions between the two pathological pathways. M
Externí odkaz:
https://doaj.org/article/837d79c860fe4baab89543f1f380e376
Autor:
Yao Yu, Zhiyi Dong, Yongjie Li, Jun Zhang, Sufeng Yin, Xuguang Gao, Shouling Wu, KaiLuan Study Investigators
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Background: The American Heart Association (AHA) defined cardiovascular health in terms of four behaviors (smoking, diet, physical activity, body weight) and three factors (plasma glucose, cholesterol, blood pressure). By this definition, the prevale
Externí odkaz:
https://doaj.org/article/7dedfcee70ed4f668c4f40488d132ba9
Autor:
Daojun Hong, Pu Fang, Sheng Yao, Juanjuan Chen, Xiaolei Zhang, Shuyun Chen, Jingfen Zhang, Dandan Tan, Li Wang, Xinsheng Han, Ling Xin, Yan Wang, Meige Liu, Lu Cong, Shanshan Zhong, Hui Ouyang, Xuguang Gao, Jun Zhang
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 9, Pp 1728-1738 (2019)
Abstract Objective To identify a new genetic cause in patients segregating distal hereditary motor neuropathy (dHMN) with an autosomal recessive pattern. Methods Whole‐exome sequencing was conducted in two siblings and was combined with segregation
Externí odkaz:
https://doaj.org/article/cb1c344e6e7445da950fdf640c7de357
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Lacunar infarcts, white matter lesions, cerebral microbleed, enlarged perivascular space and brain atrophy are regarded as magnetic resonance imaging (MRI) manifestations of cerebral small vessel disease (cSVD). 24-hour blood pressure var
Externí odkaz:
https://doaj.org/article/fc8bd21c1e614bf1978176379be2651c
Publikováno v:
Clinical Neuropathology. 41:271-276
To report a new genetic cause of distal hereditary motor neuropathy (dHMN), which is likely associated with worsening during pregnancy. We collected the clinical data of a patient with severe weakness of the lower limbs induced by repeated pregnancy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcd8895022e5e9dfd9035d93a5c8820a
https://doi.org/10.5414/np301489
https://doi.org/10.5414/np301489