Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Fei-Hong Luo"'
Autor:
Wei Wu, Jian-Wei Zhang, Yangxi Li, Ke Huang, Rui-Min Chen, Mireguli Maimaiti, Jing-Si Luo, Shao-Ke Chen, Di Wu, Min Zhu, Chun-Lin Wang, Zhe Su, Yan Liang, Hui Yao, Hai-Yan Wei, Rong-Xiu Zheng, Hong-Wei Du, Fei-Hong Luo, Pin Li, Ergang Wang, Constantin Polychronakos, Jun-Fen Fu
Publikováno v:
The Lancet Regional Health. Western Pacific, Vol 52, Iss , Pp 101206- (2024)
Summary: Background: The worldwide geographical and temporal variation in the prevalence of diabetes represents a challenge, but also an opportunity for gaining etiological insights. Encompassing the bulk of East Asians, a large and distinct proporti
Externí odkaz:
https://doaj.org/article/bcbb8c01e55740928dc4c30223fdd7c5
Autor:
Guo-Hua Li, Ke Huang, Guan-Ping Dong, Jian-Wei Zhang, Chun-Xiu Gong, Fei-Hong Luo, Xiao-Ping Luo, Chun-Lin Wang, Min Zhu, Pin Li, Ling Wang, Jun-Fen Fu, The T1DM China Study Group for Children Adolescents
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ObjectiveTo investigate the clinical incidence and characteristics of type 1 diabetes mellitus (T1DM) of children and adolescents at the time of initial diagnosis in China.MethodsData on all pediatric patients with newly diagnosed T1DM were retrospec
Externí odkaz:
https://doaj.org/article/8a5729a679f5405da8b2ab25c399ed25
Autor:
Zhen-Ran Xu, Xiao-Yi Zhu, Wei Lu, Wei-Hua Sun, Ruo-Qian Cheng, Jin-Wen Ni, Li Xi, Khalid Hussain, Fei-Hong Luo, Miao-Ying Zhang
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
BackgroundIn addition to inborn metabolic disorders, altered metabolic profiles were reported to be associated with the risk and prognosis of some non-metabolic diseases, while as a rare metabolic disease, the overall secondary metabolic spectrum in
Externí odkaz:
https://doaj.org/article/95a22a06cd104f51be33f56255dcf101
Autor:
Yang-Li, Dai1 (AUTHOR), Fei-Hong, Luo2 (AUTHOR), Hui-Wen, Zhang3 (AUTHOR), Ming-Sheng, Ma4 (AUTHOR), Xiao-Ping, Luo5 (AUTHOR), Li, Liu6 (AUTHOR), Yi, Wang2 (AUTHOR), Qing, Zhou7 (AUTHOR), Yong-Hui, Jiang8 (AUTHOR) yong-hui.jiang@yale.edu, Chao-Chun, Zou1 (AUTHOR) zcc14@zju.edu.cn, PWS Cooperation Group of Rare Diseases Branch of Chinese Pediatric Society (AUTHOR), Xiao-Ou, Shan (AUTHOR), Yu, Yang (AUTHOR), Hui-Feng, Zhang (AUTHOR), Zhi-Liang, Tian (AUTHOR), Bo, Sun (AUTHOR), Mei, Lu (AUTHOR), Ya-Ying, Cheng (AUTHOR), Ying, Yang (AUTHOR), Xiong-Ying, Yu (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 6/13/2022, Vol. 17 Issue 1, p1-13. 13p.
Autor:
Ruo-Qian Cheng, Yan-Qin Ying, Zheng-Qing Qiu, Jun-Fen Fu, Chun-Xiu Gong, Yan-Ling Yang, Wei Shi, Hui Li, Ming-Sheng Ma, Chang-Yan Wang, Min Liu, Jia-Jia Chen, Chang Su, Xiao-Ping Luo, Fei-Hong Luo, Wei Lu
Publikováno v:
World Journal of Pediatrics. 19:438-449
Background Recombinant human growth hormone (rhGH) therapy has shown to improve height and body composition in children with Prader–Willi syndrome (PWS), the evidence of early rhGH treatment on motor and mental development is still accumulating. Th
Autor:
Zhen-Ran Xu, Xiao-Xiao Yuan, Rui-Min Chen, Hai-Yan Wei, Lin-Qi Chen, Hong-Wei Du, Gui-Mei Li, Yu Yang, Xiao-Juan Chen, Xin Fang, Fei-Hong Luo
Publikováno v:
World journal of pediatrics : WJP. 18(10)
Background The real-world exposure levels of non-therapeutic antibiotics and neonicotinoids in type 1 diabetes (T1D) children and their associations as environmental triggers through gut microbiota shifts remained unknown. We thus investigated the an
Autor:
Junfen Fu, jianwei zhang, Wei Wu, Ke Huang, Ruimin Chen, Mireguli Maimaiti, Jing-Si Luo, Shao-Ke Chen, Jieming Zhong, Di Wu, Min Zhu, Chun-Lin Wang, Zhe Su, Yan Liang, Hui Yao, Haiyan Wei, Rongxiu Zheng, Hong-Wei Du, Fei-Hong Luo, Pin Li, MinJia Mo, Yun-Xian Yu, Er-Gang Wang, Robert A. Vigersky
Publikováno v:
SSRN Electronic Journal.
Autor:
Shaoke Chen, Xia Liu, Xiu Zhao, Ruimin Chen, Yi Wang, Linqi Chen, Chunxiu Gong, Yu Yang, Jin Wang, Zhe Su, Baoheng Gui, Fei-Hong Luo, Xiumin Wang, Lijun Fan, Yanning Song
Publikováno v:
Journal of Medical Genetics. 56:685-692
BackgroundThe 5α-reductase type 2 (5α-RD2) deficiency caused by mutations in the steroid 5α-reductase 2 (SRD5A2) gene results in variable degrees of undervirilisation in patients with 46,XY disorders of sex development. This study aims to profile
Autor:
Ling-Xiao, Wang, Ruo-Qian, Cheng, Miao-Ying, Zhang, Xiao-Jing, Li, Li, Xi, Zhang-Qian, Zheng, Fei-Hong, Luo
Publikováno v:
Zhongguo Dang Dai Er Ke Za Zhi
OBJECTIVE: To study the association of body fat ratio with precocious puberty in girls. Previous studies have shown that body mass index (BMI) is associated with the girls' age of puberty but have not revealed the association of body fat ratio with a
Autor:
Baoheng, Gui, Yanning, Song, Zhe, Su, Fei-Hong, Luo, Linqi, Chen, Xiumin, Wang, Ruimin, Chen, Yu, Yang, Jin, Wang, Xiu, Zhao, Lijun, Fan, Xia, Liu, Yi, Wang, Shaoke, Chen, Chunxiu, Gong
Publikováno v:
Journal of medical genetics. 56(10)
The 5α-reductase type 2 (5α-RD2) deficiency caused by mutations in the steroid 5α-reductase 2 (190 subjects diagnosed with 5α-RD2 deficiency were consecutively enrolled from eight medical centres in China. Their clinical manifestations and geneti