Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Xianqing, Ren"'
Autor:
Qingyin Guo, Xiaolei Hu, Chundong Song, Xianqing Ren, Wensheng Zhai, Ying Ding, Xia Zhang, Meng Yang, Jian Zhang, Miao Jiang
Publikováno v:
Annals of Medicine, Vol 53, Iss 1, Pp 2315-2320 (2021)
AbstractBackground IgA vasculitis (IgAV) is a common small vessel vasculitis in children. Gastrointestinal perforation (GP) rarely presents as a complication of IgAV and is not well characterized. This study is aimed to investigate the clinical featu
Externí odkaz:
https://doaj.org/article/ccab31355e95420da2faad26a84db776
Autor:
Ying Ding, Xia Zhang, Xianqing Ren, Wensheng Zhai, Liyun He, Jianping Liu, Chen Yao, Shanshan Han, Long Wang
Publikováno v:
Trials, Vol 20, Iss 1, Pp 1-11 (2019)
Abstract Background Henoch-Schönlein purpura nephritis (HSPN) is the most common secondary glomerular disease in children. Currently, the treatment for HSPN is always selected based on the Kidney Disease Improving Global Outcomes guidelines; however
Externí odkaz:
https://doaj.org/article/73051b5d0451489dbf2d9ede07875aaa
Autor:
Ping, Rong, Li, Li, Xilian, Zhang, Quanhui, Liu, Huimin, Yan, Deli, Xin, Zheng, Xue, Xianqing, Ren, Zhenqi, Wu, Rong, Ma, Junhua, Zhang
Publikováno v:
In Journal of Traditional Chinese Medicine August 2018 38(4):504-510
Autor:
Xiaoqing Yang, Qian Shen, Jiaojiao Liu, Yueli Yang, Xianqing Ren, Wensheng Zhai, Ying Ding, Xia Zhang, Meng Yang, Jian Zhang, Bo Liu, Hong Xu, Yanjie Huang
Background X-linked Alport syndrome (XLAS) has been poorly studied in girls. The aim of this study was to investigate the clinicopathological features of XLAS in girls, and find out whether α5(IV) chain immunofluorescence staining on paraffin sectio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76bf730597ef4a0ee9b51abd4dc831f4
https://doi.org/10.21203/rs.3.rs-2919799/v1
https://doi.org/10.21203/rs.3.rs-2919799/v1
Autor:
Jingjing Wu, Yingying Wen, Yuying Sun, Hang Su, Leying Xi, Shuang Xu, Xianqing Ren, Yingying Jiang
Publikováno v:
International Journal of General Medicine
Leying Xi,1 Shuang Xu,2 Yingying Jiang,2 Hang Su,2 Yuying Sun,2 Yingying Wen,2 Jingjing Wu,2 Xianqing Ren2 1Department of Pediatrics, Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, People
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a40509c65f899aa3ee7117715c962fd1
https://doi.org/10.2147/ijgm.s337437
https://doi.org/10.2147/ijgm.s337437
Publikováno v:
European journal of medical genetics. 65(12)
WT1 disorder is caused by a heterozygous variant in the gene WT1 (Wilms' tumor suppressor gene 1), and is clinically diagnosed as Denys-Drash, Meacham, or Frasier syndrome, on a phenotypic continuum that presents as abnormalities of the urogenital sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9adf0b3450529b203e2af0abed69c17d
https://pubmed.ncbi.nlm.nih.gov/36341869
https://pubmed.ncbi.nlm.nih.gov/36341869
Autor:
Chundong Song, Caiyun Wang, Dan Song, Xiaoqing Yang, Bo Zhang, Fengyang Duan, Xia Zhang, Meng Yang, Ying Ding, Xianqing Ren, Wensheng Zhai
(1) Background: To investigate the application value of Oxford pathological classification in children with henoch schonlein purpura nephritis (HSPN); (2) Methods: The clinical and pathological data of 341 children with HSPN diagnosed by renal biopsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7dbd048f39af70a980a6cf782d3f46b
https://doi.org/10.21203/rs.3.rs-1467291/v1
https://doi.org/10.21203/rs.3.rs-1467291/v1
Autor:
Xiaowei Zhang, Yingying Yan, Xianqing Ren, Weiwei He, Chaoyuan Hu, Jun-Jin Yin, Chuang Liu, Yuanyang Mao
Publikováno v:
Nanoscale. 12:3068-3075
The emerging properties of mimicking enzymes open up new horizons for nanomaterials. Regulating their enzyme-like activity and exploiting their applications are currently the hot topics for nanozymes. Among their activities, the pro-oxidant and antio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46ab4bd8d2f8f590ad28d57a450d45e2
https://doi.org/10.1039/c9nr10135g
https://doi.org/10.1039/c9nr10135g
Autor:
Panpan, Zhai, Weigang, Lv, Xiaoqing, Yang, Yanjie, Huang, Wensheng, Zhai, Xianqing, Ren, Xia, Zhang, Meng, Yang, Jian, Zhang, Ting, Guo, Minghui, Bai, Yueli, Yang, Ying, Ding, Yanshi, Huang
Publikováno v:
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. 25(4)
The study aims to explore the clinicopathological features and whether the nonsense mutations of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0758673699cc0c890386dcb3465636af
https://pubmed.ncbi.nlm.nih.gov/35100899
https://pubmed.ncbi.nlm.nih.gov/35100899
Autor:
Yanjie Huang, Wensheng Zhai, Jinghui Luo, Xiaoqing Yang, Shangsai Yue, Xiaoke Zheng, Yingbao Yang, Panpan Zhai, Xianqing Ren, Xiaofeng Mei, Tatsuo Yamamoto, Yanan Zhang, Liangliang Bi
Publikováno v:
International urology and nephrology. 54(6)
The aim was to investigate the diagnostic efficacy of urinary protein/creatinine ratio (UPCR) and factors influencing its substitutability of 24-h urine protein (24hUP) in children with proteinuria. A total of 356 children were recruited, including 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c811bae1ec978e985e7df842c0d78257
https://pubmed.ncbi.nlm.nih.gov/34668110
https://pubmed.ncbi.nlm.nih.gov/34668110