How to Approach Neutropenia in Childhood
- 1 April 2013
- journal article
- case report
- Published by American Academy of Pediatrics (AAP) in Pediatrics in Review
- Vol. 34 (4), 173-184
- https://doi.org/10.1542/pir.34-4-173
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Genetic Defects in Severe Congenital Neutropenia: Emerging Insights into Life and Death of Human Neutrophil GranulocytesAnnual Review of Immunology, 2011
- Clinical presentation and management of drug-induced agranulocytosisExpert Review of Hematology, 2011
- Congenital neutropenia: diagnosis, molecular bases and patient managementOrphanet Journal of Rare Diseases, 2011
- Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: Evidence for phenotype determination by modifying genesPediatric Blood & Cancer, 2010
- Duffy (Fy), DARC, and neutropenia among women from the United States, Europe and the CaribbeanBritish Journal of Haematology, 2008
- A molecular classification of congenital neutropenia syndromesPediatric Blood & Cancer, 2007
- Severe chronic neutropenia: Treatment and follow‐up of patients in the Severe Chronic Neutropenia International RegistryAmerican Journal of Hematology, 2003
- Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropeniaBlood, 2000
- A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (filgrastim) for treatment of severe chronic neutropeniaBlood, 1993
- Isoimmune Neonatal NeutropeniaAmerican Journal of Perinatology, 1986