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Frontiers in Pediatrics|October 17, 2022
Novel compound heterozygous CCDC40 mutations in a familial case of primary ciliary dyskinesiaLiqing Zhao, Suqiu Huang, Wei Wei, et al.
Frontiers in Pediatrics|October 17, 2022
Preoperative complications in children with mesenteric lymphatic malformations: Incidence, risk factors and outcomesJiayu Yan, Li Wang, Chuanping Xie, et al.
Frontiers in Pediatrics|October 17, 2022
Administrative data in pediatric critical care research-Potential, challenges, and future directionsNora Bruns, Anna-Lisa Sorg, Ursula Felderhoff-Müser, et al.
Frontiers in Pediatrics|October 17, 2022
Caries prevalence of the first permanent molar and associated factors among second-grade students in Xiangyun of Yunnan, China: A cross-sectional studyMingshan Liu, Xiaoqin Xu, Qianqian Song, et al.
Frontiers in Pediatrics|October 17, 2022
Antenatal care utilization and nutrition counseling are strongly associated with infant and young child feeding knowledge among rural/semi-urban women in Harari region, Eastern EthiopiaAklilu Abrham Roba, Assefa Tola, Desta Dugassa, et al.
Frontiers in Pediatrics|October 17, 2022
Supporting the diagnosis of infantile colic by a point of care measurement of fecal calprotectinHenning Sommermeyer, Malgorzata Bernatek, Marcin Pszczola, et al.
Frontiers in Pediatrics|October 17, 2022
Outcomes of endovascular embolization for Vein of Galen malformations: An individual participant data meta-analysisCody Savage, Andrew T Hale, Matthew S Parr, et al.
Frontiers in Pediatrics|October 17, 2022
A population-based study on prevalence and predisposing risk factors of infant functional gastrointestinal disorders in a single center in Southern FujianHuanhuan Huang, Caiyun Wang, Wei Lin, et al.
Frontiers in Pediatrics|October 17, 2022
Activated CD4 + T lymphocyte is a potential biomarker for acute graft-vs.-host disease after hematopoietic stem cell transplantation in children with transfusion-dependent β-thalassemiaKen Huang, Jianming Luo
Frontiers in Pediatrics|October 17, 2022
Infantile-onset Pompe disease complicated by sickle cell anemia: Case report and management considerationsRodrigo Tzovenos Starosta, Ying-Chen Claire Hou, Katelyn Leestma, et al.
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