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HIV-associated autoimmune hemolytic anemia: report of a case and review of the literature.
Telen MJ, Roberts KB, Bartlett JA. Telen MJ, et al. J Acquir Immune Defic Syndr (1988). 1990;3(10):933-7. J Acquir Immune Defic Syndr (1988). 1990. PMID: 2204697 Review.
Laboratory and clinical findings of severe hemolysis were present, including anhaptoglobinemia, microspherocytosis, splenomegaly, and transfusion dependence. Azidothymidine (AZT) therapy may have exacerbated this patient's anemia. ...
Laboratory and clinical findings of severe hemolysis were present, including anhaptoglobinemia, microspherocytosis, splenomegaly, and …
Acute intravascular haemolysis with massive microspherocytosis in a 75-year-old woman.
Perseghin P, Epis R, Pastorini A, Camerone G. Perseghin P, et al. Recenti Prog Med. 1997 Oct;88(10):459-60. Recenti Prog Med. 1997. PMID: 9401430 Review.
Blood and stool cultures were repeatedly negative, but the massive microspherocytosis, typically observed in clostridia infections, oriented our diagnosis. ...
Blood and stool cultures were repeatedly negative, but the massive microspherocytosis, typically observed in clostridia infections, o …
Altered spectrin dimer-dimer association and instability of erythrocyte membrane skeletons in hereditary pyropoikilocytosis.
Liu SC, Palek J, Prchal J, Castleberry RP. Liu SC, et al. J Clin Invest. 1981 Sep;68(3):597-605. doi: 10.1172/jci110293. J Clin Invest. 1981. PMID: 7276161 Free PMC article.
Hereditary pyropoikilocytosis (HPP) is a hemolytic anemia characterized by microspherocytosis, poikilocytosis, and an unusual thermal sensitivity of erythrocytes. ...
Hereditary pyropoikilocytosis (HPP) is a hemolytic anemia characterized by microspherocytosis, poikilocytosis, and an unusual thermal …