中国科技期刊卓越行动计划推介:《世界儿科杂志(英文)》20卷11期

科创中国 2024-12-10 13:44:31

World Journal of Pediatrics2024年第20卷第十一期,扫描二维码可跳转至官网阅读全文;

官网:

springer.com/journal/12519

01

Editorial

儿童单基因狼疮的早期临床检测模型:对数字医学未来的影响

A model for early clinical detection of pediatric monogenic lupus: implications for the future of digital medicine

CiteYang W. A model for early clinical detection of pediatric monogenic lupus: implications for the future of digital medicine. World J Pediatr. 2024 Nov;20(11):1103-1104. doi: 10.1007/s12519-024-00842-x.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00842-x

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02

Review article

疑似缺氧缺血性脑病引起的新生儿脑病:病理生理学,当前和新兴的治疗方法

Neonatal encephalopathy due to suspected hypoxic ischemic encephalopathy: pathophysiology, current, and emerging treatments

CiteBabbo CC, Mellet J, van Rensburg J, Pillay S, Horn AR, Nakwa FL, Velaphi SC, Kali GTJ, Coetzee M, Masemola MYK, Ballot DE, Pepper MS. Neonatal encephalopathy due to suspected hypoxic ischemic encephalopathy: pathophysiology, current, and emerging treatments. World J Pediatr. 2024 Nov;20(11):1105-1114. doi: 10.1007/s12519-024-00836-9.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00836-9

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癫痫基因治疗的最新进展和现状

Recent advances and current status of gene therapy for epilepsy

CiteCai AJ, Gao K, Zhang F, Jiang YW. Recent advances and current status of gene therapy for epilepsy. World J Pediatr. 2024 Nov;20(11):1115-1137. doi: 10.1007/s12519-024-00843-w.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00843-w

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03

Original article

早期随访与新生儿再入院率降低的关系:一项基于法国人口的数据关联研究

Association of early follow-up visits with reduced hospital readmissions of newborns: a French population-based data-linkage study

CiteRavel C, Nimal M, Nauleau S, Lapalus D, Bernard O, Gras E, Tardieu S, Boubred F. Association of early follow-up visits with reduced hospital readmissions of newborns: a French population-based data-linkage study. World J Pediatr. 2024 Nov;20(11):1138-1144. doi: 10.1007/s12519-024-00841-y.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00841-y

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中国重大出生缺陷患病率的时间趋势:2007年至2021年全国人口基础研究

Temporal trends in the prevalence of major birth defects in China: a nationwide population-based study from 2007 to 2021

CiteLi WY, Chen ZY, Xu WL, Gao YY, Liu Z, Li Q, Dai L. Temporal trends in the prevalence of major birth defects in China: a nationwide population-based study from 2007 to 2021. World J Pediatr. 2024 Nov;20(11):1145-1154. doi: 10.1007/s12519-024-00844-9.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00844-9

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LASSO衍生线图用于儿童单基因狼疮的早期识别

LASSO-derived nomogram for early identification of pediatric monogenic lupus

CiteZhang TY, Wang W, Gao SH, Yu ZX, Wang W, Zhou Y, Wang CY, Jian S, Wang L, Gou LJ, Li J, Ma MS, Song HM. LASSO-derived nomogram for early identification of pediatric monogenic lupus. World J Pediatr. 2024 Nov;20(11):1155-1167. doi: 10.1007/s12519-024-00817-y.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00817-y

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母亲患病与后代肾脏和泌尿道先天性异常:一项队列研究

Maternal diseases and congenital anomalies of the kidney and urinary tract in offspring: a cohort study

CiteMa Q, Li YQ, Meng QT, Yang B, Zhang HT, Shi H, Liu CY, Xiang TC, Zhao N, Rao J. Maternal diseases and congenital anomalies of the kidney and urinary tract in offspring: a cohort study. World J Pediatr. 2024 Nov;20(11):1168-1178. doi: 10.1007/s12519-024-00822-1.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00822-1

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基于全基因测序的女性生殖道先天畸形的遗传变异和分子谱系

Genetic variation and molecular profiling of congenital malformations of the female genital tract based on whole-genome sequencing

CiteQiu JJ, Chang XY, Zhang N, Guo LP, Wang S, Gu WY, Yin YM, Shi ZW, Hua KQ. Genetic variation and molecular profiling of congenital malformations of the female genital tract based on whole-genome sequencing. World J Pediatr. 2024 Nov;20(11):1179-1195. doi: 10.1007/s12519-024-00839-6.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00839-6

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04

Commentaries

产妇保健与胎儿发育:调查产妇疾病与子代肾脏和泌尿道先天性异常之间的关系

Maternal health and fetal development: investigating the connection between maternal diseases and congenital anomalies of the kidneys and urinary tract

CiteTang WZ, Huang KJ, Liu TH. Maternal health and fetal development: investigating the connection between maternal diseases and congenital anomalies of the kidneys and urinary tract. World J Pediatr. 2024 Nov;20(11):1196-1197. doi: 10.1007/s12519-024-00847-6.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00847-6

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回复“产妇保健与胎儿发育:调查产妇疾病与子代肾脏和泌尿道先天性异常之间的关系

Reply to “maternal health and fetal development: investigating the connection between maternal diseases and congenital anomalies of the kidneys and urinary tract”

CiteMa Q, Li YQ, Meng QT, Yang B, Zhang HT, Shi H, Liu CY, Xiang TC, Zhao N, Rao J. Reply to "maternal health and fetal development: investigating the connection between maternal diseases and congenital anomalies of the kidneys and urinary tract". World J Pediatr. 2024 Nov;20(11):1198-1199. doi: 10.1007/s12519-024-00851-w.

原文链接:

https://link.springer.com/article/10.1007/s12519-024-00847-6

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