Found: 21
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A novel WT1 gene mutation in a patient with Wilms' tumor and 46, XY gonadal dysgenesis.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Autoimmune thyroid disease in Libyan children and young adults with type 1 diabetes mellitus.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Persistent coagulase-negative staphylococci bacteremia in very-low-birth-weight infants.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Measurements of neonatal bilirubin and albumin concentrations: a need for improvement and quality control.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Respiratory morbidity, healthcare utilisation and cost of care at school age related to home oxygen status.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Neurological complications of pandemic influenza A H1N1 2009 infection: European case series and review.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Palliative care for children and adolescents in Switzerland: a needs analysis across three diagnostic groups.
- Published in:
- 2011
- By:
- Publication type:
- journal article
A novel mutation of LHX3 is associated with combined pituitary hormone deficiency including ACTH deficiency, sensorineural hearing loss, and short neck-a case report and review of the literature.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Adolescent alcohol intoxication in Dutch hospital centers of pediatrics: characteristics and gender differences.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Combination therapy for life-threatening pulmonary hypertension in a premature infant: first report on bosentan use.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Long-term outcomes of pneumococcal meningitis in childhood and adolescence.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Neonatal pulmonary interstitial glycogenosis in a patient with Hunter syndrome.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Reply to the correspondence letter by Hakan N et al. alendronate for the treatment of hypercalcaemia due to neonatal subcutaneous fat necrosis.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Application of the new pediatric criteria and Tel Hashomer criteria in heterozygous patients with clinical features of FMF.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Early diagnosis of cerebral X-linked adrenoleukodystrophy in boys with Addison's disease improves survival and neurological outcomes.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Diagnosis and management of acute pharyngitis in a paediatric population: a cost-effectiveness analysis.
- Published in:
- 2011
- By:
- Publication type:
- journal article
LEOPARD syndrome (PTPN11, T468M) in three boys fulfilling neurofibromatosis type 1 clinical criteria.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Alendronate for the treatment of hypercalcaemia due to neonatal subcutaneous fat necrosis.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Eponym : Grisel syndrome.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Clinical practice : diagnosis and treatment of functional constipation.
- Published in:
- 2011
- By:
- Publication type:
- journal article