PURE RED CELL APLASIA IN CHILDHOOD AND ADOLESCENCE: PATHOGENESIS AND APPROACHES TO DIAGNOSIS
- 1 October 1993
- journal article
- review article
- Published by Wiley in British Journal of Haematology
- Vol. 85 (2) , 246-253
- https://doi.org/10.1111/j.1365-2141.1993.tb03163.x
Abstract
No abstract availableThis publication has 81 references indexed in Scilit:
- Increase of CALLA-positive stimulated lymphoid cells in transient erythroblastopenia of childhoodEuropean Journal of Pediatrics, 1990
- Reduced neutrophil counts in children with transient erythroblastopenia of childhoodThe Journal of Pediatrics, 1989
- Pure Red-Cell Aplasia of 10 Years' Duration Due to Persistent Parvovirus B19 Infection and Its Cure with Immunoglobulin TherapyNew England Journal of Medicine, 1989
- Treatment of Antibody-Mediated Pure Red-Cell Aplasia with High-Dose Intravenous Gamma GlobulinNew England Journal of Medicine, 1987
- Chronic Bone Marrow Failure Due to Persistent B19 Parvovirus InfectionNew England Journal of Medicine, 1987
- Elevated Erythrocyte Adenosine Deaminase Activity in Congenital Hypoplastic AnemiaNew England Journal of Medicine, 1983
- Severe anemia in childhood presenting as transient ischemic attacks.Stroke, 1983
- Control of Antibody-Mediated Pure Red-Cell Aplasia by PlasmapheresisNew England Journal of Medicine, 1981
- Bone-Marrow Microenvironment Defect in Congenital Hypoplastic AnemiaNew England Journal of Medicine, 1980
- Normal Erythropoietic Helper T Cells in Congenital Hypoplastic (Diamond-Blackfan) AnemiaNew England Journal of Medicine, 1978