Works matching IS 03406199 AND DT 2010 AND VI 169 AND IP 2
Results: 22
DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Long-term treatment with recombinant insulin-like growth factor 1 (IGF-1) in a child with IGF-1 gene mutation.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Programmed death-1 (PD-1) gene polymorphisms lodged in the genetic predispositions of Kawasaki Disease.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Rupture of the papillary muscle of the tricuspid valve - echocardiographic diagnosis of a rare anomaly leading to critical tricuspid valve regurgitation in the newborn.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Characteristics associated with maltreatment types in children referred to a hospital protection team.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Does lack of routine postnatal examination on maternity unit increase the risk of hospital admission in the first week of life?
- Published in:
- 2010
- By:
- Publication type:
- journal article
Fulminant hepatitis B and acute hepatitis B due to intrafamilial transmission of HBV after chemotherapy for non-Hodgkin's lymphoma in an HBV carrier.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Titration of betaine therapy to optimize therapy in an infant with 5,10-methylenetetrahydrofolate reductase deficiency.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Increased type 3 iodothyronine deiodinase activity in a regrown hepatic hemangioma with consumptive hypothyroidism.
- Published in:
- 2010
- By:
- Publication type:
- journal article
A heritable cause of cleft lip and palate--Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Clinical practice: an approach to stridor in infants and children.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Reply to correspondence letter by M. Das et al.: WHO Child Growth Standards.
- Published in:
- 2010
- By:
- Publication type:
- Letter
A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Clinical practice: the hip from birth to adolescence.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Maternal bariatric surgery: adverse outcomes in neonates.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Surveillance study of apparent life-threatening events (ALTE) in the Netherlands.
- Published in:
- 2010
- By:
- Publication type:
- journal article
A 4-year-old boy presenting with recurrent croup.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Favourable long-term outcome after immediate treatment of neonatal hyperammonemia due to N-acetylglutamate synthase deficiency.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Pneumococcal pneumonia--is it underdiagnosed?
- Published in:
- 2010
- By:
- Publication type:
- commentary
WHO child growth standards.
- Published in:
- 2010
- By:
- Publication type:
- commentary
Significance of long-chain polyunsaturated fatty acids (PUFAs) for the development and behaviour of children.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Streptococcus pneumoniae-associated haemolytic uremic syndrome following influenza A virus infection.
- Published in:
- 2010
- By:
- Publication type:
- journal article