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期刊名:Archives of disease in childhood

缩写:ARCH DIS CHILD

ISSN:0003-9888

e-ISSN:1468-2044

IF/分区:3.2/Q1

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共收录本刊相关文章索引19414
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Dean Robinson,Catherine Rennie,Claire Hogg et al. Dean Robinson et al.
Objective: This retrospective observational study aimed to examine the associations among genetic mutations, demographic characteristics and hearing outcomes in children diagnosed with primary ciliary dyskinesia (PCD). By...
Sophie T Brouard,Yaël Pinhas,Jérémie F Cohen et al. Sophie T Brouard et al.
Objective: To assess the proportion of pictures of sleeping infants or infant sleep environments that are inconsistent with safe infant sleep recommendations (SISRs) in the visual exposome of infant caretakers. ...
Laura Ojanperä,Lauri Lehtimäki,Balázs Kelemen et al. Laura Ojanperä et al.
Background: Research on spacers for paediatric breathing patterns is limited, especially for disposable types, which may be a practical alternative to reusable valved holding chambers (VHC) in certain clinical settings. ...
Chandrika Bhat,Florence Martin,Devika Chennakeshava et al. Chandrika Bhat et al.
Objective: Severe dengue in children may present with a hyperinflammatory phenotype resembling cytokine storm or secondary haemophagocytic lymphohistiocytosis, characterised by refractory shock, hepatic dysfunction and mu...
Hannah Vennard,Anna Selby,Menaga Ananthamoorthy et al. Hannah Vennard et al.
Background and objective: Cardiorespiratory polygraphy (CRP) is the predominant technology used to diagnose obstructive sleep apnoea (OSA) in tertiary centres in the UK. Nocturnal pulse oximetry (NPO) is cheaper and more ...
Anouk Olthof,Marelle J Bouva,Hedi L Claahsen-van der Grinten et al. Anouk Olthof et al.
Objective: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is an inherited adrenal steroid synthesis disorder included in Dutch newborn screening (NBS) since 2002. Screening involves measuring 17-hyd...