References
- Men, S. and larva, H. (1998) "Complement regulation", Vox Sang. 2\(Suppl. 2 , 291–302.
- Frank, M.M. (1987) "Complement in the pathophysiology of human disease", N. Engl. J. Med. 316, 1525–1530.
- Lublin, D.M. and Atkinson, J.P. (1989) "Decay accelerating factor: biochemistry, molecular biology and function", Ann. Rev. Immunol. 7, 35–58.
- Walport, M.J. (2001) "Complement. First of two parts", N. Engl. J. Med. 344, 1058–1066.
- Luzzatto, L. and Bessler, M. (1996) "The dual pathogenesis of PNH", Curr. Opin. Hematol. 3, 101–110.
- Karadimitris, A. and Luzzatto, L. (2001) "The cellular pathogenesis of paroxysmal nocturnal haemoglobinuria", Leukemia 15, 1148–1152.
- Tremml, G., Karadimitris, A. and Lizzatto, L. (1998) "Paroxysmal nocturnal hemoglobinuria: learning about PNH cells from patients and mice", Haema 1, 12–20.
- Holt, D.S., Botto, M., Bygrave, A.E., Hanna, S.M., Walport, M.J. and Morgan, B.P. (2001) "Targeted deletion of the CD59 gene causes spontaneous intravascular hemolysis and hemoglobinuria", Blood 98, 442–449.
- Rosse, W.F. (2001) "New insights into paroxysmal nocturnal hemoglobinuria", Curr. Opin. Hematol. 8, 61–67.
- Dunn, D.E., Tanawattanacharoen, P., Boccuni, P., Nagakura, S., Green, S.W., Kirby, M.R., Rosenfeld, S. and Young, N.S. (1999) "Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes", Ann. Intern. Med. 131, 401–408.
- Meletis, J. and Terpos, E. (2001) "Paroxysmal nocturnal haemoglobinuria: clinical presentation and association with other haematological disorders", Haema 4, 79–88.
- Meletis, J., Terpos, E., Samarkos, M., Meletis, C., Konstantopoulos, K., Komninaka, V., Apostolidou, E., Benopoulou, O., Korovesis, K., Mavrogianni, D., Variami, E., Yataganas, X. and Loukopoulos, D. (2001) "Detection of CD55 and/or CD59 deficient red cell populations in patients with aplastic anemia, myelodysplastic syndromes and myeloproliferative disorders", Haematologia 31, 7–16.
- Meletis, J., Terpos, E., Samarkos, M., Meletis, C., Apostolidou, E., Komninaka, V, Korovesis, K., Mavrogianni, D., Boutsis, D., Variami, E., Viniou, N., Konstantopoulos, K. and Loukopoulos, D. (2001) "Detection of CD55 and/or CD59 deficient red cell populations in patients with lymphoproliferative syndromes", Hematol. J. 2, 33–37.
- Meletis, J., Terpos, E., Samarkos, M., Meletis, C., Apostolidu, E., Komninaka, V, Korovesis, K., Anargyrou, K., Benopoulou, O., Mavrogianni, D., Variami, E., Viniou, N. and Konstantopoulos, K. (2002) "Detection of CD55 and/or CD59 deficient red cell populations in patients with plasma cell dyscrasias", Int. J. Hematol., 75, 40–44.
- Hara, T., Kojima, A., Fukuda, H., Masaoka, T., Fukumori, Y., Matsumoto, M. and Seya, T. (1992) "Levels of complement regulatory proteins, CD35 (CR1), CD46 (MCP) and CD55 (DAF) in human haematological malignancies", Br. J. Haematol. 82, 368–373.
- Seya, T., Tejima, H., Fukuda, H., Hara, T., Matsumoto, M., Hatanaka, M., Sugita, Y. and Masaoka, T. (1993) "Acute promyelocytic leukaemia with CD59 deficiency", Leuk. Res. 17, 895–896.
- Guc, D., Canpinar, H., Kucukaksu, C. and Kansu, E. (2000) "Expression of complement regulatory proteins CR1, DAF, MCP and CD59 in haematological malignancies", Fur. J. Haematol. 64, 3–9.
- Grimwade, D., Walker, H., Harrison, G., Oliver, F., Chatters, S., Harrison, C.J., Wheatley, K., Burnett, A.K. and Gold-stone, A.H. (2001) "The predictive value of hierarchical cytogenetic classification in older adults with acute myeloid leukaemia (AML): analysis of 1065 patients entered into the UK Medical Research Council AML11 trial", Blood 98, 1312–1320.
- Nilsson, B., Hagstrom, U., Englund, A. and Safwenberg, J. (1993) "A simplified assay for the specific diagnosis of Paroxysmal Nocturnal Hemoglobinuria: Detection of DAF (CD55)- and HRF20 (CD59)- erythrocytes in microtyping cards", Vox Sang. 64, 43–46.
- Meletis, J., Michali, E., Samarkos, M., Konstantopoulos, K., Meletis, C., Terpos, E., Tsimberidou, A., Chandrinou, E., Viniou, N., Rombos, Y., Pangalis, GA., Yataganas, X. and Loukopoulos, D. (1997) "Detection of "PNH Red Cell" populations in hematological disorders using the sepha-cryl gel test micro typing system", Leuk. Lymphoma 28, 177–182.
- Harris, J.W., Koscick, R., Lazarus, H.M., Eshleman, J.R. and Medof, M.E. (1999) "Leukemia arising out of paroxysmal nocturnal hemoglobinuria", Leuk. Lymphoma 32, 401–426.
- Stafford, HA., Nagarajan, S., Weinberg, J.B. and Medof, M.E. (1995) "PIG-A, DAF and proto-oncogene expression in paroxysmal nocturnal haemoglobinuria-associated acute myelogenous leukaemic blasts", Br. J. Haematol. 89, 72–78.
- Kwong, Y.L., Lee, C.P., Chan, T.K. and Chan, T.C. (1994) "Flow cytometric measurement of glycosylphosphatidyl-inositol-linked surface proteins on blood cells of patients with paroxysmal nocturnal hemoglobinuria", Am. J. Clin. Pathol. 102, 30–35.
- Sun, X., Funk, CD., Deng, C., Sahu, A., Lambris, J.D. and Song, W.C. (1999) "Role of decay-accelerating factor in regulating complement activation on the erythrocyte surface as revealed by gene targeting", Proc. Natl Acad. Sci. USA 96, 628–633.
- Hatanaka, M., Seya, T., Matsumoto, M., Hara, T., Nonaka, M., Inoue, N., Takeda, J. and Shimizu, A. (1996) "Mechanisms by which the surface expression of the glycosyl-phosphatidyl-inositol-anchored complement regulatory proteins decay-accelerating factor (CD55) and CD59 is lost in human leukaemia cell lines", Biochem. J. 314, 969–976.
- Seya, T., Hara, T., Matsumoto, M. and Akedo, H. (1990) "Quantitative analysis of membrane cofactor protein (MCP) of complement. High expression of MCP on human leukemia cell lines, which is down regulated during cell differen-tiation", J. Immunol. 145, 238–245.
- Araten, D., Nafa, K., Pakdeesuwan, K. and Luzzatto, L. (1999) "Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals", Proc. Natl Acad. Sci. USA 96, 5209–5214.
- Yamaguchi, M., Machii, T., Azenishi, Y., Nishimura, J., Shibano, M., Kanakura, Y. and Kitani, T. (2000) "Detection of small population of CD59-deficient erythrocytes in patients with aplastic anemia or myelodysplastic syn-dromes and normal individuals", Blood Cells Mol. Dis. 26, 247–254.
- Rawstron, AC., Rollinson, S.J., Richards, S., Short, M.A., English, A., Morgan, G.J., Hale, G. and Hillmen, P. (1999) "The PNH phenotype cells that emerge in most patients after CAMPATH-1H therapy are present prior to treatment", Br. J. Haematol. 107, 148–153.