[Association between insulin resistance and idiopathic central precocious puberty in girls and the diagnostic value of insulin resistance] [0.03%]
女孩胰岛素抵抗与中枢性早熟的相关性及其诊断价值
Jin-Bo Li,Ya Xiao,Shu-Qin Jiang et al.
Jin-Bo Li et al.
Objectives: To explore the relationship between insulin resistance and idiopathic central precocious puberty (ICPP) in girls and the diagnostic value of insulin resistance. ...
[Efficacy and safety of ibuprofen for the treatment of patent ductus arteriosus in preterm infants of different postnatal ages] [0.03%]
不同胎龄早产儿应用布洛芬治疗动脉导管未闭疗效及安全性分析
Di Wen,Yang Liu,Ping-Ren Chen et al.
Di Wen et al.
Objectives: To evaluate the efficacy and safety of ibuprofen in treating hemodynamically significant patent ductus arteriosus (hsPDA) in preterm infants of different postnatal ages at treatment initiation. ...
[Metabolomic alterations in preterm infants with bronchopulmonary dysplasia] [0.03%]
早产儿支气管肺发育不良的代谢组学变化
Yan-Yan Wu,Qi-Qi Bu,Xin Wang et al.
Yan-Yan Wu et al.
Objectives: To analyze the serum metabolomic changes of preterm infants with bronchopulmonary dysplasia (BPD) at postmenstrual age (PMA) 36 weeks, screen potential biomarkers and associated metabolic pathways, and assess ...
[Development of dynamic multi-time-point clinical prediction models for bronchopulmonary dysplasia in preterm infants with gestational age < 32 weeks] [0.03%]
极早早产儿(
Wen Li,Xue-Fei Zhang,Xiao-Ri He et al.
Wen Li et al.
Objectives: To develop dynamic prediction models based on multiple postnatal time points to support early diagnosis and individualized intervention for bronchopulmonary dysplasia (BPD) in preterm infants with gestational ...
Run-Mei Zou,Cheng Wang
Run-Mei Zou
Vasovagal syncope (VVS) is the most common cause of neurally mediated syncope in children. Recurrent syncope severely affects physical and mental health and may lead to unintentional injury. Based on international and domestic guidelines an...
[Comprehensive considerations for the diagnosis, treatment, and management of osteogenesis imperfecta] [0.03%]
[I型骨质生成不全的诊断、治疗和管理]
Xiang-Hong Lyu,Jian Dong
Xiang-Hong Lyu
Osteogenesis imperfecta (OI) is a rare genetic skeletal disorder most commonly caused by variants in COL1A1 and COL1A2, which encode type I collagen. It is characterized by increased bone fragility, recurrent fractures, and skeletal deformi...
[Expert recommendations on antenatal counseling for extremely preterm infants] [0.03%]
极早产儿的antenatal咨询专家建议
Hunan Neonatal Medical Quality Control Center;Perinatal Committee of Hunan Medical Association
Hunan Neonatal Medical Quality Control Center;Perinatal Committee of Hunan Medical Association
With continuous advancements in neonatal care in China, the survival rate of extremely preterm infants has markedly increased in recent years. However, the proportion of voluntary withdrawal of treatment for extremely preterm infants remain...
[Guidelines for the diagnosis and treatment of common neonatal diseases in primary healthcare institutions: neonatal jaundice (2025)] [0.03%]
基层医疗机构新生儿常见病规范化诊治指南：新生儿黄疸（2025）
Subspecialty Group of Neonatology;Society of Pediatrics, Chinese Medical Association; Editorial Board of ChineseJournal of Contemporary Pediatrics
Subspecialty Group of Neonatology;Society of Pediatrics
To better assist primary healthcare providers in recognizing the importance of postnatal bilirubin monitoring, and in developing the ability to promptly identify neonatal jaundice that requires intervention and to provide appropriate evalua...
[The microbiota-gut-brain axis in childhood attention-deficit/hyperactivity disorder: mechanisms and therapeutic advances] [0.03%]
儿童注意缺陷多动障碍的微生态-肠-脑轴研究：机制和治疗进展
Ying-Lun Yuan,Yong-Mei Lan,Lin-Mei Guo
Ying-Lun Yuan
Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder in children. Growing evidence links ADHD to gut microbiota dysbiosis, positioning the microbiota-gut-brain axis as a new focus of childhood ADHD researc...
[The application of machine learning in the auxiliary diagnosis of specific learning disorder] [0.03%]
基于机器学习的特定学习障碍辅助诊断应用研究
Hao Zhao,Shu-Lan Mei,Jing-Yu Wang et al.
Hao Zhao et al.
Specific learning disorder (SLD) is a common neurodevelopmental disorder in children that significantly affects academic performance and quality of life. At present, diagnosis mainly relies on standardized tests and professional evaluations...