Vertical transmission of HIV-1 infection and dilemma of infant feeding
Does circadian variation in risk factors for sudden infant death syndrome (SIDS) suggest there are two (or more) SIDS subtypes?
The size of the thymus
Do we need another NSAID instead of indomethacin for treatment of ductus arteriosus in preterm infants?
Identifying children at risk for language impairment
Children and statins
Overnight central and peripheral temperature changes in normal infants
Circadian variations in sudden infant death syndrome
Birth season and environmental influences on patterns of thymic growth in rural Gambian infants
Oesophageal pH monitoring in children
Urinary 8-hydroxydeoxyguanosine excretion in children before and after therapy for eradication of Helicobacter pylori infection
Pubertal growth and development in cystic fibrosis
Improved final height in Turner's syndrome following growth-promoting treatment at a single centre
Longitudinal growth and height velocity of Japanese children with Down's syndrome
Influence of dietary intervention on growth in children with hypercholesterolaemia
Chediak-Higashi syndrome
Glomerular filtration rate
Supraventricular tachycardia
Diaphragm dimensions of the healthy term infant
Haemodynamic features during high-frequency oscillatory ventilation in preterms
Tolerance to early human milk feeding is not compromised by indomethacin in preterm infants with persistent ductus arteriosus
Postnatal adaptation of cerebral blood flow using near infrared spectroscopy in extremely preterm infants undergoing high-frequency oscillatory ventilation
Neonatal hypotonia
Identifying children at risk for language impairment
Quality of life, anxiety and concerns among statin-treated children with familial hypercholesterolaemia and their parents.
Pregnancy and childbirth-related factors associated with recurrent antibiotic use in infants
Pinpoint skin lesions in a familial hypercholesterolaemia homozygote
Growth failure and diabetes in cystic fibrosis
Severe venous thrombosis in an infant heterozygous for the G20210A mutation in the prothrombin gene