Skip to main content
The Western Journal of Medicine logoLink to The Western Journal of Medicine
. 1980 Mar;132(3):219–228.

Paroxysmal nocturnal hemoglobinuria--present status and future prospects.

W F Rosse
PMCID: PMC1272021  PMID: 7376658

Full text

PDF
227

Selected References

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

  1. Aster R. H., Enright S. E. A platelet and granulocyte membrane defect in paroxysmal nocturnal hemoglobinuria: usefulness for the detection of platelet antibodies. J Clin Invest. 1969 Jul;48(7):1199–1210. doi: 10.1172/JCI106084. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brubaker L. H., Essig L. J., Mengel C. E. Neutrophil life span in paroxysmal nocturnal hemoglobinuria. Blood. 1977 Oct;50(4):657–662. [PubMed] [Google Scholar]
  3. COHEN P., GARDNER F. H., BARNETT G. O. Reclassification of the thrombocytopenias by the Cr51-labeling method for measuring platelet life span. N Engl J Med. 1961 Jun 22;264:1294–contd. doi: 10.1056/NEJM196106222642506. [DOI] [PubMed] [Google Scholar]
  4. Charache S. Prolonged survival in paroxysmal nocturnal hemoglobinuria. Blood. 1969 Jun;33(6):877–883. [PubMed] [Google Scholar]
  5. Craddock P. R., Fehr J., Jacob H. S. Complement-mediated granulocyte dysfunction in paroxysmal nocturnal hemoglobinuria. Blood. 1976 Jun;47(6):931–939. [PubMed] [Google Scholar]
  6. DACIE J. V. Paroxysmal nocturnal haemoglobinuria. Proc R Soc Med. 1963 Jul;56:587–596. [PMC free article] [PubMed] [Google Scholar]
  7. Dameshek W. Foreword and a proposal for considering paroxysmal nocturnal hemoglobinuria (PNH) as a "candidate" myeloproliferative disorder. Blood. 1969 Feb;33(2):263–264. [PubMed] [Google Scholar]
  8. Dixon R. H., Rosse W. F. Mechanism of complement-mediated activation of human blood platelets in vitro: comparison of normal and paroxysmal nocturnal hemoglobinuria platelets. J Clin Invest. 1977 Feb;59(2):360–368. doi: 10.1172/JCI108648. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Fefer A., Freeman H., Storb R., Hill J., Singer J., Edwards A., Thomas E. Paroxysmal nocturanal hemoglobinuria and marrow failure treated by infusion of marrow from an identical twin. Ann Intern Med. 1976 Jun;84(6):692–695. doi: 10.7326/0003-4819-84-6-692. [DOI] [PubMed] [Google Scholar]
  10. Firkin F., Goldberg H., Firkin B. G. Glucocorticoid management of paroxysmal nocturnal haemoglobinuria. Australas Ann Med. 1968 May;17(2):127–134. doi: 10.1111/imj.1968.17.2.127. [DOI] [PubMed] [Google Scholar]
  11. Greenberg P., Mara B., Bax I., Brossel R., Schrier S. The myeloproliferative disorders. Correlation between clinical evolution and alterations of granulopoiesis. Am J Med. 1976 Dec;61(6):878–891. doi: 10.1016/0002-9343(76)90412-5. [DOI] [PubMed] [Google Scholar]
  12. Ham T. H., Dingle J. H. STUDIES ON DESTRUCTION OF RED BLOOD CELLS. II. CHRONIC HEMOLYTIC ANEMIA WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA: CERTAIN IMMUNOLOGICAL ASPECTS OF THE HEMOLYTIC MECHANISM WITH SPECIAL REFERENCE TO SERUM COMPLEMENT. J Clin Invest. 1939 Nov;18(6):657–672. doi: 10.1172/JCI101081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hansen N. E., Killmann S. A. Paroxysmal nocturnal haemoglobinuria. A clinical study. Acta Med Scand. 1968 Dec;184(6):525–541. [PubMed] [Google Scholar]
  14. Hartmann R. C., Jenkins D. E., Jr, McKee L. C., Heyssel R. M. Paroxysmal nocturnal hemoglobinuria: clinical and laboratory studies relating to iron metabolism and therapy with androgen and iron. Medicine (Baltimore) 1966 Sep;45(5):331–363. doi: 10.1097/00005792-196609000-00001. [DOI] [PubMed] [Google Scholar]
  15. Holden D., Lichtman H. Paroxysmal nocturnal hemoglobinuria with acute leukemia. Blood. 1969 Feb;33(2):283–286. [PubMed] [Google Scholar]
  16. Jenkins D. E., Jr, Hartmann R. C. Paroxysmal nocturnal hemoglobinuria terminating in acute myeloblastic leukemia. Blood. 1969 Feb;33(2):274–282. [PubMed] [Google Scholar]
  17. Lewis S. M., Dacie J. V. The aplastic anaemia--paroxysmal nocturnal haemoglobinuria syndrome. Br J Haematol. 1967 Mar;13(2):236–251. doi: 10.1111/j.1365-2141.1967.tb08736.x. [DOI] [PubMed] [Google Scholar]
  18. Moore M. A., Williams N., Metcalf D. In vitro colony formation by normal and leukemic human hematopoietic cells: characterization of the colony-forming cells. J Natl Cancer Inst. 1973 Mar;50(3):603–623. doi: 10.1093/jnci/50.3.603. [DOI] [PubMed] [Google Scholar]
  19. Oni S. B., Osunkoya B. O., Luzzatto L. Paroxysmal nocturnal hemoglobinuria: evidence for monoclonal origin of abnormal red cells. Blood. 1970 Aug;36(2):145–152. [PubMed] [Google Scholar]
  20. Peytremann R., Rhodes R. S., Hartmann R. C. Thrombosis in paroxysmal nocturnal hemoglobinuria (PNH) with particular reference to progressive, diffuse hepatic venous thrombosis. Ser Haematol. 1972;5(3):115–136. [PubMed] [Google Scholar]
  21. Rickard K. A., Brown R. D., Wilkinson T., Kronenberg H. The colony forming cell in the myeloproliferative disorders and aplastic anaemia. Scand J Haematol. 1979 Feb;22(2):121–128. doi: 10.1111/j.1600-0609.1979.tb00412.x. [DOI] [PubMed] [Google Scholar]
  22. Rosse W. F., Adams J. P., Thorpe A. M. The population of cells in paroxysmal nocturnal haemoglobinuria of intermediate sensitivity to complement lysis: significance and mechanism of increased immune lysis. Br J Haematol. 1974 Oct;28(2):181–190. doi: 10.1111/j.1365-2141.1974.tb06652.x. [DOI] [PubMed] [Google Scholar]
  23. Rosse W. F., Dacie J. V. Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. The sensitivity of PNH red cells to lysis by complement and specific antibody. J Clin Invest. 1966 May;45(5):736–748. doi: 10.1172/JCI105388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Rosse W. F., Gutterman L. A. The effect of iron therapy in paroxysmal nocturnal hemoglobinuria. Blood. 1970 Nov;36(5):559–565. [PubMed] [Google Scholar]
  25. Rosse W. F., Logue G. L., Adams J., Crookston J. H. Mechanisms of immune lysis of the red cells in hereditary erythroblastic multinuclearity with a positive acidified serum test and paroxysmal nocturnal hemoglobinuria. J Clin Invest. 1974 Jan;53(1):31–43. doi: 10.1172/JCI107551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Rosse W. F. Paroxysmal nocturnal haemoglobinuria in aplastic anaemia. Clin Haematol. 1978 Oct;7(3):541–553. [PubMed] [Google Scholar]
  27. Rouault T. A., Rosse W. F., Bell S., Shelburne J. Differences in the terminal steps of complement lysis of normal and paroxysmal nocturnal hemoglobinuria red cells. Blood. 1978 Feb;51(2):325–330. [PubMed] [Google Scholar]
  28. Stern M., Rosse W. F. Two populations of granulocytes in paroxysmal nocturnal hemoglobinuria. Blood. 1979 May;53(5):928–934. [PubMed] [Google Scholar]
  29. Storb R., Thomas E. D., Weiden P. L., Buckner C. D., Clift R. A., Fefer A., Fernando L. P., Giblett E. R., Goodell B. W., Johnson F. L. Aplastic anemia treated by allogeneic bone marrow transplantation: a report on 49 new cases from Seattle. Blood. 1976 Dec;48(6):817–841. [PubMed] [Google Scholar]
  30. Sultan C., Marquet M., Joffroy Y. Etude de certaines dysmyélopoièses acquises idiopathiques et secondaires par culture de moelle in vitro. Ann Med Interne (Paris) 1974 Jun-Jul;125(6-7):599–602. [PubMed] [Google Scholar]
  31. Tsevrenis H., Pouggouras P., Simos A., Contopoulou I., Papazacharias A., Dariotis A. Evolution d'une hémoglobinurie nocturne paroxystique, maladie de Marchiafava-Micheli, en leucose aiguë. Nouv Rev Fr Hematol. 1970 Mar-Apr;10(2):274–277. [PubMed] [Google Scholar]

Articles from Western Journal of Medicine are provided here courtesy of BMJ Publishing Group

RESOURCES