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ObjectiveThis study examined whether caregivers’ picture book reading styles involving moral narratives are associated with the strength of their belief in a just world.MethodsWe investigated the relationship between c...

IntroductionSTING-associated vasculopathy with onset in infancy (SAVI) is a rare, severe type I interferonopathy caused by gain-of-function mutations in STING1, leading to early-onset systemic inflammation, cutaneous vas...

Introduction:Attention deficit hyperactivity disorder (ADHD) is a neuropsychiatric pathology that has an important prevalence among young people and is difficult to diagnose. It is usually treated with methylphenidate, a...

IntroductionHaploinsufficiency of A20 (HA20) is a monogenic autoinflammatory disorder caused by heterozygous loss-of-function variants in TNFAIP3, resulting in dysregulated NF-κB activation. Clinical presentations are h...

Subjects / keywords: BOWER, T.G.R; W.H. FREEMAN AND COMPANY; 155.4 B786d

Subjects / keywords: KEITH, JOHN; MACMILLAN PUBLISHING; 616.12 K28h3

Subjects / keywords: NATHAN, DAVID G; W. B. SAUNDERS COMPANY; 618.9221 N274h2

Subjects / keywords: BELSKY, JAY; COLUMBIA UNIVERSITY PRESS; 155.422 I35i

Subjects / keywords: BORSTEIN, MARC H; LAWRENCE ERLBAUM ASSOCIATES; 155.4 B736p

Chronic renal failure (CRF) is defined as a serum creatinine above 1mg/dl in the 1st year of life, which corresponds to creatinine clearances below 30ml/min per 1.73m². CRF is rarely seen in the newborn period. Acco...

Neonatal seizures are most commonly attributed to hypoxic-ischaemic injury, metabolic abnormalities, or central nervous system infections; however, an increasing proportion of cases are recognised to have an underlying g...

Abstract Melatonin plays a key role in circadian regulation, and its interaction with the gut microbiota may be critical for early-life development. Beyond its circadian function, melatonin dysregulation is implicated in...

Bullous pemphigoid is an autoimmune blistering disease that very rarely affects children. Clinical differences in locations of skin lesions led to the distinction of infantile versus childhood pemphigoid. Mucous membrane...

The experiences of recent years have tested all public sectors, and society has faced challenges we would not have foreseen. This has transformed our society into one that is more global, resilient and sustainable, and w...

Abstract Objectives This study aimed to examine the clinical characteristics of Chinese patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGLD) and identify the prevalent mutations in the HMGCL gene among t...

Illicit arms trafficking in Ukraine has been a significant issue since the Cold War, with leftover Soviet stockpiles providing lucrative smuggling routes. With over US$100 billion in aid being provided by the West, a siz...

Hoyeraal-Hreidarsson syndrome (HHS) represents the most severe form of dyskeratosis congenita (DC), a telomere biology disorder caused by pathogenic variants in genes involved in telomere maintenance. DKC1 encodes dysker...

West syndrome (WS) is the most common epileptic syndrome in infancy characterised by epileptic spasms, hypsarrhythmia and neurodevelopmental problems. Epileptic spasms remain in many ways a conundrum, and the ideal inter...