Red cell aplasia responsive to immunoglobulin therapy as initial manifestation of human immunodeficiency virus infection
- 31 March 1992
- journal article
- case report
- Published by Elsevier in The American Journal of Medicine
- Vol. 92 (3) , 331-333
- https://doi.org/10.1016/0002-9343(92)90085-p
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Human ParvovirusesThe Journal of Infectious Diseases, 1990
- 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
- Childhood transient erythroblastopenia complicated by thrombocytopenia and neutropeniaEuropean Journal of Haematology, 1989
- Hematologic aspects of human immunodeficiency virus infection: Laboratory and clinical considerationsAmerican Journal of Hematology, 1988
- Human T cell leukemia virus-I-associated T-suppressor cell inhibition of erythropoiesis in a patient with pure red cell aplasia and chronic T gamma-lymphoproliferative disease.Journal of Clinical Investigation, 1988
- Haematologic manifestations of the human immune deficiency virus (HIV)British Journal of Haematology, 1987
- Hematologic abnormalities in the acquired immune deficiency syndromeThe American Journal of Medicine, 1984
- Pure Red-Cell AplasiaNew England Journal of Medicine, 1974
- Bone-Marrow Failure Due to Relative Nutritional Deficiency in Cooley's Hemolytic AnemiaNew England Journal of Medicine, 1959