Department of Paediatrics & Adolescent Medicine
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Recent Submissions
Congenital and Paediatric Acquired Heart Disease in Practice
Transcriptomic features of systemic lupus erythematosus patients in flare and changes during acute in-hospital treatment
Association of vitamin D-binding protein polymorphisms and serum 25(OH)D concentration varies among Chinese healthy infants of different VDR-FokI genotypes: A multi-centre cross-sectional study
Identifying a possible mechanism for Sudden Infant Death with Dysgenesis of Testes Syndrome (SIDDT)
Building a baby-friendly community: Development, strategy, implementation and evaluation of a BFCI program
Effect of a Mobile Game–Based Intervention to Enhance Child Safety: Randomized Controlled Trial
Benefits v. risks of COVID-19 vaccination: an examination of vaccination policy impact on the occurrence of myocarditis and pericarditis
Maternal diabetes and risk of attention-deficit/hyperactivity disorder in offspring in a multinational cohort of 3.6 million mother–child pairs
The central role of natural killer cells in mediating acute myocarditis after mRNA COVID-19 vaccination
Early social experiences and later psychopathology: the role of OXTR rs53576 genotype
Oxytocin receptor gene polymorphism (rs53576) and depressive symptoms: a systematic review and meta-analysis
A systematic review on the applicability of cell-free DNA level as an obesity biomarker
Prospective associations of maternal stressors with child psychosocial problems through the occurrence of child physical abuse and changes in family dynamics
Longitudinal associations between child discipline methods and physical growth patterns across preschool years
Early-life family and school impacts on adolescent conduct problems: A path analysis
Identification and functional analysis of first heterozygous frameshift mutation in the GHRH gene in a Chinese boy with isolated growth hormone deficiency
Association of genetic variation on X chromosome with systemic lupus erythematosus in both Thai and Chinese populations
Functional investigation of a novel ANKRD11 frameshift variant identified in a Chinese family with KBG syndrome
Molecular diagnosis is an important indicator for response to growth hormone therapy in children with short stature
Genome-wide association study of BNT162b2 vaccine-related myocarditis identifies potential predisposing functional areas in Hong Kong adolescents