Goldstein AR , Anderson MJ, Serjeant GRParvovirus associated aplastic crisis in homozygous sickle cell disease. Arch Dis Child.1987;62:585-588.
2.
Saarinen UM, Chorba TL, Tattersail P., et al. Human parvovirus B19-induced epidemic acute red cell aplasia in patients with hereditary hemolytic anemia. Blood. 1986;67:1411-1417.
3.
Mann MC, Votto J., McNamee MJManagement of the severely anemic patient who refuses transfusion: lessons learned during the care of a Jehovah's Witness. Ann Intern Med.1992; 117:1042-1048.
4.
Sherwood JB, Goldwasser E., Chilote R., et al. Sickle cell anemia patients have low erythropoietin levels for their degree of anemia. Blood. 1986;67:46-49.
5.
Nagel RL, Vichinsky W., Shah M., et al. F reticulocyte response in sickle cell anemia treated with recombinant human erythropoietin: a double-blind study. Blood. 1993;81:9-14.
6.
Ozawa K., Kurtzman G., Young N.Replication of the B19 parvovirus in human bone marrow cell cultures. Science. 1986;233:883-886.
7.
Austin T., Uchiyama N., Katz J.Treatment of child with erythropoietin (EPO) and granulocytic colony stimulating factor (G-CSF) presenting with erythroblastopenia and neutropenia secondary to human parvovirus B19 infection and complicated by cellulitis and mastoiditis . Proceedings of American Society of Pediatric Hematology/Oncology . 1992;1:30. Abstract.
8.
Koch WC, Massey G., Russell CE, Adler SPManifestations and treatment ofhuman parvovirus B19 infection in immunocompromised patients. J Pediatr.1990;116:355-359.
9.
Kurtzman G., Frickhofen N., Kimball J., et al. Pure red-cell aplasia of 10 years' duration due to persistent parvovirus B19 infection and its cure with immunoglobulin therapy. N Engl J Med.1989; 321:519-523.
10.
Hanada T., Koike K., Takeya T., et al. Human parvovirus B19-induced transient pancytopenia in a child with hereditary spherocytosis. Br J Haematol.1988;70:113-115.