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MeSH Review

Anemia, Hemolytic

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  1. Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Clinical experience in 108 patients. Bell, W.R., Braine, H.G., Ness, P.M., Kickler, T.S. N. Engl. J. Med. (1991) [Pubmed]
  2. Hemolytic anemia and erythroleukemia, two distinct pathogenic effects of Friend MuLV: mapping of the effects to different regions of the viral genome. Sitbon, M., Sola, B., Evans, L., Nishio, J., Hayes, S.F., Nathanson, K., Garon, C.F., Chesebro, B. Cell (1986) [Pubmed]
  3. Type-I interferon receptor deficiency reduces lupus-like disease in NZB mice. Santiago-Raber, M.L., Baccala, R., Haraldsson, K.M., Choubey, D., Stewart, T.A., Kono, D.H., Theofilopoulos, A.N. J. Exp. Med. (2003) [Pubmed]
  4. Biochemical heterogeneity in glutathione synthetase deficiency. Spielberg, S.P., Garrick, M.D., Corash, L.M., Butler, J.D., Tietze, F., Rogers, L., Schulman, J.D. J. Clin. Invest. (1978) [Pubmed]
  5. Variation of erythroid and myeloid precursors in the marrow and peripheral blood of volunteer subjects infected with human parvovirus (B19). Potter, C.G., Potter, A.C., Hatton, C.S., Chapel, H.M., Anderson, M.J., Pattison, J.R., Tyrrell, D.A., Higgins, P.G., Willman, J.S., Parry, H.F. J. Clin. Invest. (1987) [Pubmed]
  6. Splenic accumulation of Tc-99m HMDP in a patient with severe alcoholic cirrhosis of the liver. Kawamura, E., Kawabe, J., Hayashi, T., Oe, A., Kotani, J., Torii, K., Habu, D., Shiomi, S. Clinical nuclear medicine. (2005) [Pubmed]
  7. The role of metabolite-specific antibodies in nomifensine-dependent immune hemolytic anemia. Salama, A., Mueller-Eckhardt, C. N. Engl. J. Med. (1985) [Pubmed]
  8. Hemolytic anemia after tetracycline therapy. Simpson, M.B., Pryzbylik, J., Innis, B., Denham, M.A. N. Engl. J. Med. (1985) [Pubmed]
  9. Positive direct antiglobulin tests and immune hemolytic anemia in patients receiving procainamide. Kleinman, S., Nelson, R., Smith, L., Goldfinger, D. N. Engl. J. Med. (1984) [Pubmed]
  10. Letter: ESR and Coombs-positive hemolytic anemia. Ballas, S.K. N. Engl. J. Med. (1975) [Pubmed]
  11. Role of CD47 as a marker of self on red blood cells. Oldenborg, P.A., Zheleznyak, A., Fang, Y.F., Lagenaur, C.F., Gresham, H.D., Lindberg, F.P. Science (2000) [Pubmed]
  12. Thiazide-induced immune hemolytic anemia. Vila, J.M., Blum, L., Dosik, H. JAMA (1976) [Pubmed]
  13. Long-term administration of massive doses of Sn-protoporphyrin in anemic mutant mice (sphha/sphha). Sassa, S., Drummond, G.S., Bernstein, S.E., Kappas, A. J. Exp. Med. (1985) [Pubmed]
  14. Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemia. Baronciani, L., Beutler, E. J. Clin. Invest. (1995) [Pubmed]
  15. A rabbit reticulocyte model for the role of hemin-controlled repressor in hypochromic anemias. Freedman, M.L., Rosman, J. J. Clin. Invest. (1976) [Pubmed]
  16. Spectrofluorescent detection of in vivo red cell lipid peroxidation in patients treated with diaminodiphenylsulfone. Goldstein, B.D., McDonagh, E.M. J. Clin. Invest. (1976) [Pubmed]
  17. Features associated with, and the impact of, hemolytic anemia in patients with systemic lupus erythematosus: LX, results from a multiethnic cohort. Durán, S., Apte, M., Alarcón, G.S., Marion, M.C., Edberg, J.C., Kimberly, R.P., Zhang, J., Langefeld, C.D., Vilá, L.M., Reveille, J.D. Arthritis Rheum. (2008) [Pubmed]
  18. Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease. Tutois, S., Montagutelli, X., Da Silva, V., Jouault, H., Rouyer-Fessard, P., Leroy-Viard, K., Guénet, J.L., Nordmann, Y., Beuzard, Y., Deybach, J.C. J. Clin. Invest. (1991) [Pubmed]
  19. Drosophila development requires spectrin network formation. Deng, H., Lee, J.K., Goldstein, L.S., Branton, D. J. Cell Biol. (1995) [Pubmed]
  20. Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice. Peters, L.L., Birkenmeier, C.S., Bronson, R.T., White, R.A., Lux, S.E., Otto, E., Bennett, V., Higgins, A., Barker, J.E. J. Cell Biol. (1991) [Pubmed]
  21. Resistance to apoptosis caused by PIG-A gene mutations in paroxysmal nocturnal hemoglobinuria. Brodsky, R.A., Vala, M.S., Barber, J.P., Medof, M.E., Jones, R.J. Proc. Natl. Acad. Sci. U.S.A. (1997) [Pubmed]
  22. Targeted disruption of Nrf2 causes regenerative immune-mediated hemolytic anemia. Lee, J.M., Chan, K., Kan, Y.W., Johnson, J.A. Proc. Natl. Acad. Sci. U.S.A. (2004) [Pubmed]
  23. Crystal structure of the repetitive segments of spectrin. Yan, Y., Winograd, E., Viel, A., Cronin, T., Harrison, S.C., Branton, D. Science (1993) [Pubmed]
  24. ATP depletion as a consequence of adenosine deaminase inhibition in man. Siaw, M.F., Mitchell, B.S., Koller, C.A., Coleman, M.S., Hutton, J.J. Proc. Natl. Acad. Sci. U.S.A. (1980) [Pubmed]
  25. Erythropoiesis in ha/ha and sph/sph mice, mutants which produce spectrin-deficient erythrocytes. Brookoff, D., Maggio-Price, L., Bernstein, S., Weiss, L. Blood (1982) [Pubmed]
  26. Sucrose density gradient analysis of erythrocyte membranes in hemolytic anemias. Flynn, T.P., Johnson, G.J., Allen, D.W. Blood (1981) [Pubmed]
  27. Generalized hexokinase deficiency in the blood cells of a patient with nonspherocytic hemolytic anemia. Rijksen, G., Akkerman, J.W., van den Wall Bake, A.W., Hofstede, D.P., Staal, G.E. Blood (1983) [Pubmed]
  28. Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia. Beutler, E., Carson, D., Dannawi, H., Forman, L., Kuhl, W., West, C., Westwood, B. J. Clin. Invest. (1983) [Pubmed]
  29. Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia. Vulliamy, T.J., D'Urso, M., Battistuzzi, G., Estrada, M., Foulkes, N.S., Martini, G., Calabro, V., Poggi, V., Giordano, R., Town, M. Proc. Natl. Acad. Sci. U.S.A. (1988) [Pubmed]
  30. Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man. Birkenmeier, C.S., McFarland-Starr, E.C., Barker, J.E. Proc. Natl. Acad. Sci. U.S.A. (1988) [Pubmed]
  31. Evidence for a susceptibility gene (SLEH1) on chromosome 11q14 for systemic lupus erythematosus (SLE) families with hemolytic anemia. Kelly, J.A., Thompson, K., Kilpatrick, J., Lam, T., Nath, S.K., Gray-McGuire, C., Reid, J., Namjou, B., Aston, C.E., Bruner, G.R., Scofield, R.H., Harley, J.B. Proc. Natl. Acad. Sci. U.S.A. (2002) [Pubmed]
  32. Thrombosis and secondary hemochromatosis play major roles in the pathogenesis of jaundiced and spherocytic mice, murine models for hereditary spherocytosis. Kaysser, T.M., Wandersee, N.J., Bronson, R.T., Barker, J.E. Blood (1997) [Pubmed]
  33. Thrombotic microangiopathy and renal failure associated with antineoplastic chemotherapy. Jackson, A.M., Rose, B.D., Graff, L.G., Jacobs, J.B., Schwartz, J.H., Strauss, G.M., Yang, J.P., Rudnick, M.R., Elfenbein, I.B., Narins, R.G. Ann. Intern. Med. (1984) [Pubmed]
  34. Glucose-6-phosphate isomerase deficiency associated with nonspherocytic hemolytic anemia in the mouse: an animal model for the human disease. Merkle, S., Pretsch, W. Blood (1993) [Pubmed]
  35. Diethylstilbestrol-associated hemolytic anemia with a positive direct antiglobulin test result. Rosenfeld, C.S., Winters, S.J., Tedrow, H.E. Am. J. Med. (1989) [Pubmed]
  36. Microangiopathic hemolytic anemia in renal allotransplantation. Repart of a successfully treated case and review of the literature. Magalhaes, R.L., Braun, W.E., Straffon, R.A., Hoffman, G.C., Shainoff, J.R., Osborne, G., Deodhar, S.D. Am. J. Med. (1975) [Pubmed]
  37. Sensitive enzymatic assay for erythrocyte creatine with production of methylene blue. Okumiya, T., Jiao, Y., Saibara, T., Miike, A., Park, K., Kageoka, T., Sasaki, M. Clin. Chem. (1998) [Pubmed]
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