Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Danqun Jin"'
Autor:
Xin Ding, Gang Liu, Suyun Qian, Jiansheng Zeng, Ying Wang, Jianping Chu, Qing Chen, Jianli Chen, Yuanyuan Duan, Danqun Jin, Jiaotian Huang, Xiulan Lu, Yanmei Guo, Xiaona Shi, Ximin Huo, Jun Su, Yibing Cheng, Yi Yin, Xiaowei Xin, Zhengyun Sun, Shaodong Zhao, Hongjun Miao, Zixuan Lou, Jun Li, Jinghui Jiang, Shengying Dong
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ObjectiveTo investigate the epidemiology and the effectiveness of resuscitation from cardiopulmonary arrest (CPA) among critically ill children and adolescents during pediatric intensive care unit (PICU) stay across China.MethodsA prospective multice
Externí odkaz:
https://doaj.org/article/5e8a240fec4d43d79c9980475aaa1a4c
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-3 (2021)
Abstract Background Community-acquired infections of Pseudomonas aeruginosa (P. aeruginosa) occur very rarely. Case presentation P. aeruginos was detected in cultures of venous blood and peritoneal exudate of a newborn with 58 perforations in the sma
Externí odkaz:
https://doaj.org/article/f211c93775654628af4bdafb118acd05
Autor:
Merel A. Post, Isis de Wit, Fokje S. M. Zijlstra, Udo F. H. Engelke, Arno van Rooij, John Christodoulou, Tiong Yang Tan, Anna Le Fevre, Danqun Jin, Joy Yaplito‐Lee, Beom Hee Lee, Karen J. Low, Andrew A. Mallick, Katrin Õunap, James Pitt, William Reardon, Mari‐Anne Vals, Saskia B. Wortmann, Hans J. C. T. Wessels, Melissa Bärenfänger, Clara D. M. van Karnebeek, Dirk J. Lefeber
Publikováno v:
Journal of Inherited Metabolic Disease, 46, 2, pp. 313-325
Post, M A, De Wit, I, Zijlstra, F, Low, K J, Van Karnebeek, C, Lefeber, D & et, A 2023, ' MOGS-CDG : quantitative analysis of the diagnostic Glc3Man tetrasaccharide and clinical spectrum of six new cases ', Journal of Inherited Metabolic Disease, vol. 46, no. 2, pp. 313-325 . https://doi.org/10.1002/jimd.12588, https://doi.org/10.1002/jimd.12588
Journal of Inherited Metabolic Disease, 46, 313-325
Post, M A, De Wit, I, Zijlstra, F, Low, K J, Van Karnebeek, C, Lefeber, D & et, A 2023, ' MOGS-CDG : quantitative analysis of the diagnostic Glc3Man tetrasaccharide and clinical spectrum of six new cases ', Journal of Inherited Metabolic Disease, vol. 46, no. 2, pp. 313-325 . https://doi.org/10.1002/jimd.12588, https://doi.org/10.1002/jimd.12588
Journal of Inherited Metabolic Disease, 46, 313-325
Contains fulltext : 290862.pdf (Publisher’s version ) (Open Access) Congenital disorders of glycosylation (CDG) are a clinically and biochemically heterogeneous subgroup of inherited metabolic disorders. Most CDG with abnormal N-glycosylation can b
Publikováno v:
Transl Pediatr
BACKGROUND: The high affinity immunoglobulin-Fc fragment receptor I CD64 on neutrophils is widely assumed to be a useful biomarker in the early identification of sepsis, and it improves outcomes. We aimed to determine its ability to diagnose sepsis a
Publikováno v:
Journal of Human Genetics. 65:627-631
Herein, we present a Chinese infant with an early-onset intellectual developmental disorder with cardiac arrhythmia syndrome. A 6-month-old boy visited our hospital because of convulsions and paroxysmal cyanosis for 1 day. Mental development analysis
Autor:
Wei Zou, Hao Ding, Yang Shen, Rongqiang Yang, Sheng Yao, Xiaole Li, Jing Shan, Yuanyuan Xu, Danqun Jin
Background One of the surgical treatments for necrotising enterocolitis (NEC) is to resect the necrotic bowel and defunction the gut by stoma, which can come with severe complications impacting infant growth. Human breastmilk feeding has been proved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afb6d0cfc4b9e73451c7e9b776f12146
https://doi.org/10.21203/rs.3.rs-842262/v1
https://doi.org/10.21203/rs.3.rs-842262/v1
Publikováno v:
Journal of Human Genetics. 64:265-268
This study is to present two Chinese siblings who were diagnosed with congenital disorders of glycosylation (CDG) IIb because of mannosyl-oligosaccharide glucosidase (MOGS) deficiency. The siblings visited our hospital due to “pulmonary infection
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-3 (2021)
BMC Pediatrics
BMC Pediatrics
Background Community-acquired infections of Pseudomonas aeruginosa (P. aeruginosa) occur very rarely. Case presentation P. aeruginos was detected in cultures of venous blood and peritoneal exudate of a newborn with 58 perforations in the small intest
Publikováno v:
Journal of Molecular Neuroscience. 62:255-261
Multiple mitochondrial dysfunctions syndrome (MMDS) is an autosomal recessive disorder of systemic energy metabolism. This study is to present the diagnosis of two MMDS Chinese sufferers. Physical and auxiliary examination was performed. Next generat
Publikováno v:
Zhonghua wei zhong bing ji jiu yi xue. 31(8)
To investigate the risk factors and prognosis of acute kidney injury (AKI) in children with sepsis in pediatric intensive care unit (PICU).A retrospective analysis of clinical data of PICU sepsis children in Anhui Children's Hospital from May 2015 to