Results 121 to 130 of about 1,235 (149)
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Autoimmune Hemolytic Anemia with Reticulocytopenia and Erythroid Marrow
New England Journal of Medicine, 1982IN the course of a hemolytic disorder, episodes may occur during which reticulocytes virtually disappear from the blood, with the result that uncompensated destruction of red cells leads to progressively severe anemia. "Aplastic crises" were first described in hereditary spherocytosis1 and have been observed in many other hemolytic states, including ...
Paul M Ness, Donald R Branch, C L Conley
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Autoimmune Hemolytic Anemia With Reticulocytopenia
JAMA - Journal of the American Medical Association, 1980In four cases of autoimmune hemolytic disease, rapidly developing anemia was associated with reticulocytopenia despite intensely erythroid bone marrow. Transfusions had been withheld because compatible blood could not be obtained, and each patient was virtually moribund on admission. Type-specific RBCs were administered promptly without reaction.
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Birth Defects Research Part B: Developmental and Reproductive Toxicology, 2011
AbstractThe artemisinin antimalarials cause embryo death and malformations in animals by killing embryonic erythroblasts. Groups of pregnant rats (N = 4) were administered 35 and 48 µmol/kg artesunate and 17.2, 28.7, 48, 96, and 191 µmol/kg artelinic acid as a single oral dose on gestational day (GD) 12. Litters were examined on GD21.
Robert L Clark
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AbstractThe artemisinin antimalarials cause embryo death and malformations in animals by killing embryonic erythroblasts. Groups of pregnant rats (N = 4) were administered 35 and 48 µmol/kg artesunate and 17.2, 28.7, 48, 96, and 191 µmol/kg artelinic acid as a single oral dose on gestational day (GD) 12. Litters were examined on GD21.
Robert L Clark
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Cold Haemagglutinin Disease with Severe Anaemia, Reticulocytopenia and Erythroid Bone Marrow
Scandinavian Journal of Haematology, 1983A quantitative assessment of total, effective and ineffective erythropoiesis, and mean red cell life‐span was performed in 2 patients with idiopathic cold‐haemagglutinin disease (CHAD) who had severe anaemia, reticulocytopenia and erythroid bone marrow.
Mario Cazzola, Giovanni Barosi
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Journal of Pediatric Hematology/Oncology, 2015
In a patient with sickle cell disease receiving chronic transfusion, exacerbation of anemia with reticulocytopenia must prompt consideration of a delayed hemolytic transfusion reaction with hyperhemolysis, as further transfusion may worsen this condition; definitive diagnosis is sometimes difficult.
Madhav Vissa, Scott T Miller
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In a patient with sickle cell disease receiving chronic transfusion, exacerbation of anemia with reticulocytopenia must prompt consideration of a delayed hemolytic transfusion reaction with hyperhemolysis, as further transfusion may worsen this condition; definitive diagnosis is sometimes difficult.
Madhav Vissa, Scott T Miller
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Prolonged reticulocytopenia in autoimmune hemolytic anemia of childhood
Journal of Pediatrics, 1980Jay Greenberg +2 more
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Linezolid-associated reticulocytopenia
Annals of Hematology, 2016Danielle H Oh +2 more
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Profound sustained reticulocytopenia and anaemia in an adult patient with sickle cell disease
Transfusion Medicine, 2014Eva Lee
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Reticulocytopenia in Trichinellosis
The Journal of Parasitology, 1984This study characterizes the peripheral blood, erythrocytic profile of mice experimentally infected per os with three different doses of Trichinella spiralis larvae. Such results have not been previously detailed despite reports of hemorrhagic episodes associated with the disease (Gould, S. E., 1970. In Trichinosis in man and animals, S. E. Gould (ed.).
B Z, Ngwenya, B L, Capaci
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