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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1981 | 1 |
1988 | 1 |
1990 | 1 |
1997 | 1 |
2018 | 1 |
2024 | 0 |
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HIV-associated autoimmune hemolytic anemia: report of a case and review of the literature.
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 …
What happens to the microspherocytosis of hereditary spherocytosis in folate deficiency?
Blecher TE.
Blecher TE.
Clin Lab Haematol. 1988;10(4):403-8. doi: 10.1111/j.1365-2257.1988.tb01188.x.
Clin Lab Haematol. 1988.
PMID: 3250788
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Whole-exome sequencing enables correct diagnosis and surgical management of rare inherited childhood anemia.
Khurana M, Edwards D, Rescorla F, Miller C, He Y, Sierra Potchanant E, Nalepa G.
Khurana M, et al.
Cold Spring Harb Mol Case Stud. 2018 Oct 1;4(5):a003152. doi: 10.1101/mcs.a003152. Print 2018 Oct.
Cold Spring Harb Mol Case Stud. 2018.
PMID: 30275003
Free PMC article.
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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 …
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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 …
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