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. 1970 Jun;46(6):397–410.

Hereditary hemolytic disorders.

E R Jaffé
PMCID: PMC1749702  PMID: 5267233

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abel H. R., Bradley T. B., Jr, Ranney H. M. Pathophysiology of the hemoglobinopathies. Clin Obstet Gynecol. 1969 Mar;12(1):15–48. doi: 10.1097/00003081-196903000-00002. [DOI] [PubMed] [Google Scholar]
  2. Benesch R., Benesch R. E. Intracellular organic phosphates as regulators of oxygen release by haemoglobin. Nature. 1969 Feb 15;221(5181):618–622. doi: 10.1038/221618a0. [DOI] [PubMed] [Google Scholar]
  3. Beutler E. Effect of flavin compounds on glutathione reductase activity: in vivo and in vitro studies. J Clin Invest. 1969 Oct;48(10):1957–1966. doi: 10.1172/JCI106162. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. CUTTING H. O., MCHUGH W. J., CONRAD F. G., MARLOW A. A. AUTOSOMAL DOMINANT HEMOLYTIC ANEMIA CHARACTERIZED BY OVALOCYTOSIS; A FAMILY STUDY OF SEVEN INVOLVED MEMBERS. Am J Med. 1965 Jul;39:21–34. doi: 10.1016/0002-9343(65)90242-1. [DOI] [PubMed] [Google Scholar]
  5. Carrell R. W., Lehmann H. The unstable haemoglobin haemolytic anaemias. Semin Hematol. 1969 Apr;6(2):116–132. [PubMed] [Google Scholar]
  6. Chapman R. G. Red cell aldolase deficiency in hereditary spherocytosis. Br J Haematol. 1969 Jan-Feb;16(1):145–156. doi: 10.1111/j.1365-2141.1969.tb00386.x. [DOI] [PubMed] [Google Scholar]
  7. Charache S., Conley C. L., Waugh D. F., Ugoretz R. J., Spurrell J. R. Pathogenesis of hemolytic anemia in homozygous hemoglobin C disease. J Clin Invest. 1967 Nov;46(11):1795–1811. doi: 10.1172/JCI105670. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Fairbanks V. F., Fernandez M. N. The identification of metabolic errors associated with hemolytic anemia. JAMA. 1969 Apr 14;208(2):316–320. [PubMed] [Google Scholar]
  9. LOCK S. P., SMITH R. S., HARDISTY R. M. Stomatocytosis: a hereditary red cell anomally associated with haemolytic anaemia. Br J Haematol. 1961 Jul;7:303–314. doi: 10.1111/j.1365-2141.1961.tb00341.x. [DOI] [PubMed] [Google Scholar]
  10. Oski F. A., Naiman J. L., Blum S. F., Zarkowsky H. S., Whaun J., Shohet S. B., Green A., Nathan D. G. Congenital hemolytic anemia with high-sodium, low-potassium red cells. Studies of three generations of a family with a new variant. N Engl J Med. 1969 Apr 24;280(17):909–916. doi: 10.1056/NEJM196904242801701. [DOI] [PubMed] [Google Scholar]
  11. Taddeini L., Watson C. J. The clinical porphyrias. Semin Hematol. 1968 Oct;5(4):335–369. [PubMed] [Google Scholar]
  12. Valentine W. N., Hsieh H. S., Paglia D. E., Anderson H. M., Baughan M. A., Jaffé E. R., Garson O. M. Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome. N Engl J Med. 1969 Mar 6;280(10):528–534. doi: 10.1056/NEJM196903062801003. [DOI] [PubMed] [Google Scholar]
  13. Zarkowsky H. S., Oski F. A., Sha'afi R., Shohet S. B., Nathan D. G. Congenital hemolytic anemia with high sodium, low potassium red cells. I. Studies of membrane permeability. N Engl J Med. 1968 Mar 14;278(11):573–581. doi: 10.1056/NEJM196803142781101. [DOI] [PubMed] [Google Scholar]

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