Editorial introductions
Direct-to-consumer genetic testing
Holoprosencephaly: recommendations for diagnosis and management
Spinal muscular atrophy: a time for screening
Pharmacogenomics in pediatric leukemia
Mitochondrial genetic diseases
Growing spectrum and relevance of pediatric neuro-immunology
Biomarkers of inflammatory and auto-immune central nervous system disorders
Emerging concepts in pediatric-onset multiple sclerosis and related disorders
Diagnosing central nervous system vasculitis in children
Update on anti-N-methyl-D-aspartate receptor encephalitis in children and adolescents
Update on diagnosis, treatment, and prognosis in opsoclonus–myoclonus–ataxia syndrome
The interplay of infection and genetics in acute necrotizing encephalopathy
Anti-IgE in the treatment of allergic disorders in pediatrics
Oral immunotherapy for food allergy
Treatment of autoinflammatory syndromes
Encouraging healthy beverage intake in child care and school settings
The hospitalist movement in general pediatrics
New treatments for infant colic
Treating uncomplicated malaria in children: comparing artemisinin-based combination therapies
Children's oral health and the role of the pediatrician
Prenatal genetic screening and diagnosis for pediatricians
Endocrine disruptors, travel-associated illness, and media violence: important health considerations for children and adolescents
How to best deliver care to children with chronic illness: cystic fibrosis as a model
Not all rickets is vitamin D deficiency
Current World Literature