Works matching IS 03406199 AND DT 2009 AND VI 168 AND IP 3
Results: 23
Saccharomyces boulardii in childhood.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Comment on: Bartter syndrome and cholelithiasis in an infant: is this a mere coincidence? (Eur J Pediatr 2008;167(1):109-110).
- Published in:
- 2009
- By:
- Publication type:
- Case Study
Parental perception of weight and weight-related behaviour in 2- to 4-year-old children in the eastern part of the Netherlands.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Abstracts for the Congress in Goettingen, 19–20 February 2009.
- Published in:
- 2009
- Publication type:
- Abstract
A novel DAX1 gene mutation in a Turkish infant with X-linked adrenal hypoplasia congenita.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Influence of dietary lipids on the erythrocyte antioxidant status of hypercholesterolaemic children.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Parental perception of weight and weight-related behaviour in 2- to 4-year-old children in the eastern part of the Netherlands.
- Published in:
- 2009
- By:
- Publication type:
- Correction Notice
Reply to correspondence letter by Jae Il Shin and Jae Seung Lee: Bartter syndrome and cholelithiasis in an infant: is this a mere coincidence?
- Published in:
- 2009
- By:
- Publication type:
- Letter
Vanishing spleen after Nissen fundoplication: a case report.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Insulin resistance markers in term, normoweight neonates. The Mérida cohort.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Transition from insulin to sulfonylurea in a child with diabetes due to a mutation in KCNJ11 encoding Kir6.2--initial and long-term response to sulfonylurea therapy.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Late-onset adrenal hypoplasia congenita caused by a novel mutation of the DAX-1 gene.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Neonatal pertussis presenting as acute bronchiolitis: direct detection of the Bordetella pertussis genome using loop-mediated isothermal amplification.
- Published in:
- 2009
- By:
- Publication type:
- journal article
A case of Listeria meningoencephalitis complicated by hydrocephalus in an immunocompetent infant.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Tracheobronchial anatomy and the distribution of inhaled foreign bodies in children.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Anomalous ascending aorta causing severe compression of the left bronchus in an infant with ventricular septal defect and pulmonary atresia.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Granulomatous hepatitis, perihepatic lymphadenopathies, and autoantibody positivity: an unusual association in a child with hepatitis C.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Does diagnostic delay result in decreased survival in paediatric brain tumours?
- Published in:
- 2009
- By:
- Publication type:
- journal article
Early neurological impairment and severe anemia in a newborn with Pearson syndrome.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Intractable secretory diarrhea in a Japanese boy with mitochondrial respiratory chain complex I deficiency.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Infantile systemic hyalinosis presenting as intractable infantile diarrhea.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Human papilloma virus (HPV) infection in children and adolescents.
- Published in:
- 2009
- By:
- Publication type:
- journal article