Works matching IS 03406199 AND DT 2003 AND VI 162 AND IP 10
Results: 21
Congenital toxoplasmosis: assessment of risk to newborns in confirmed and uncertain maternal infection.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Chronic eosinophilic ascites in a very young child.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Chronic infantile neurological cutaneous articular syndrome: CD10 over-expression in neutrophils is a possible key to the pathogenesis of the disease.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Solitary thyroid nodule as presenting symptom of Pendred syndrome caused by a novel splice-site mutation in intron 8 of the SLC26A4 gene.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Infant stroke and beta-2-glycoprotein 1 antibodies: six cases.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Chronic illness, life style and emotional health in adolescence: results of a cross-sectional survey on the health of 15-20-year-olds in Switzerland.
- Published in:
- 2003
- By:
- Publication type:
- journal article
The late consequences of anthracycline treatment on left ventricular function after treatment for childhood cancer.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Surfactant therapy in neonates with respiratory failure due to haemorrhagic pulmonary oedema.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Continuous subcutaneous insulin infusion in toddlers.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Acquired angioedema and Helicobacter pylori infection in a child.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Fructose 1,6 diphosphatase deficiency in a Turkish infant.
- Published in:
- 2003
- By:
- Publication type:
- Case Study
Primary Sjögren syndrome in the paediatric age: a multicentre survey.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Paroxetine withdrawal in a neonate with historical and laboratory confirmation.
- Published in:
- 2003
- By:
- Publication type:
- journal article
An unspecific immunostimulating agent and juvenile dermatomyositis: enhanced T-cell proliferation and reverse immunosuppression as a severe adverse drug reaction.
- Published in:
- 2003
- By:
- Publication type:
- journal article
A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Experience of continuous haemodiafiltration in a male neonate with ornithine transcarbamylase deficiency.
- Published in:
- 2003
- By:
- Publication type:
- journal article
An 8-year-old boy with a 4-day history of fever, cough and malaise, and a 2-day history of painful calves and difficulty walking.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Smith OP, Hann IM (eds): Essential paediatric haematology: M. Dunitz, London, 2002. X 241 pp with illustrations and tables (ISBN 90-5823-179-8), US$ 68.
- Published in:
- European Journal of Pediatrics, 2003, v. 162, n. 10, p. 733, doi. 10.1007/s00431-003-1244-5
- By:
- Publication type:
- Article
A4 Integrin Antibody Successful in Adult Crohn Disease.
- Published in:
- European Journal of Pediatrics, 2003, v. 162, n. 10, p. 734, doi. 10.1007/s00431-003-1167-1
- Publication type:
- Article