References
- Crosby WH. Paroxysmal nocturnal hemoglobinuria: a classic description by Paul Strübing in 1882, and a bibliography of the disease. Blood 1951;6:270–84.
- Sirchia G, Lewis S.M. Paroxysmal nocturnal haemoglobinuria. Clin Haematol 1975;4:199–229.
- Rosse WE Paroxysmal nocturnal hemoglobinuria as a molecular disease. Medicine 1997;76:63–93.
- Rosse WF, Ware RE. The molecular basis of paroxysmal noctural hemoglobinuria. Blood 1995; 86:3277–86.
- Ware RE, Hall SE, Rosse WE Paroxysmal nocturnal hemoglobinuria with onset in childhood and adolescence. N Engl J Med 1991;325:991–6.
- Ware RE, Rosse WF, Howard TA. Mutations within, the PIG-A gene in patients with paroxysmal nocturnal hemoglobinuria. Blood 1994;83:2418-22.
- Dacie JV, Lewis SM. Paroxysmal nocturnal hemoglobinuria: clinical manifestations, haematology, and nature of the disease. Sem Haematol 1972;5:3-23
- Blum SF, Sullivan JM, Gardner FH.The exacerbation of hemolysis in paroxysmal nocturnal hemoglobinuria by strenuous exercise. Blood 1967;30:513-7.
- Clark DA, Butler SA, Braren V Hartmann. RC, Jenkins DE Jr. The kidneys in paroxysmal nocturnal hemoglobinuria. Blood 1981;57:83–9.
- Parker CJ, Lee GR. Paroxysmal nocturnal hemoglobinuria. In: Lee GR, Foerster J, Lukens J, Wintrobe MM, eds. Wintrobe’s clinical hematology. Baltimore, MD: Williams and Wilkins, 1999:1264–88.
- Socie G, Mary JY, de Gramont A, et al. Paroxysmal nocturnal haemoglobinuria: long-term follow-up and. prognostic factors. French Society of Haematology. Lancet 1996;348:573–7.
- Rosse WF, Dacie JV 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;45:736–48.
- Rosse WF, Dacie JV Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. II. The role of complement components in the increased sensitivity of PNH red cells to immune lysis. J Clin Invest 1966;45:749–57.
- Hillmen P, Lewis SM, Bessler M, Luzzatto L, Dacie JV Natural history of paroxysmal nocturnal hemoglobinuria. N Engl J Med 1995;333:1253–8.
- Rosse WF, Hoffman S, Campbell M, Borowitz M, Moore JO, Parker CJ. The erythrocytes in paroxysmal nocturnal haemoglobinuria of intermediate sensitivity to complement lysis. Br J Haematol 1991; 79:99–107.
- Rosse WF. The life-span of complement-sensitive and-insensitive red cells in paroxysmal nocturnal hemoglobinuria. Blood. 1971;37:556–62.
- Luzzatto L, Bessler M, Rotoli B. Somatic mutations in paroxysmal nocturnal hemoglobinuria: a blessing in disguise? Cell 1997:88:1–4.
- Rotoli B,Robledo R,Luzzatto L. Decreased number of circulating BFU-Es in paroxysmal nocturnal hemoglobinuria. Blood 1982;60: 157–9
- Young NS. The problem of clonality in aplastic anemia: Dr Dameshek’s riddle, restated. Blood 1992; 79:1385–92.
- Araten DJ, Nafa K, Pakdeesuwan K, Luzzatto L. Clonal populations of hematopoietic cells with, paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals. Proc Natl Acad Sci USA 1999;96:5209-14.
- Rotoli B, Luzzatto L. Paroxysmal nocturnal haemoglobinuria. Baillieres Clin Haematol 1989; 2:113–38.
- Telen MJ, Rosse WF, Parker CJ, Moulds MK, Moulds JJ. Evidence that several high-frequency human blood group antigens reside on phosphatidylinositol-linked erythrocyte membrane proteins. Blood 1990; 75:1404–7.
- Miyata T, Yamada N, Iida Y, et al. Abnormalities of PIG-A transcripts in granulocytes from, patients with paroxysmal nocturnal hemoglobinuria. N Engl J Med 1994;330:249–55.
- Miyata T, Takeda J, Iida Y et al. The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis. Science 1993;259:1318–20.
- Maugard C, Margueritte G.Tuffery S,Rabesandratana H, Demaille J, Claustres M. Recurrent PIG-A mutation (IVS5+1G→A) in a paediatric case of paroxysmal nocturnal haemoglobinuria: detection by the protein truncation, test. Br J Haematol 1997;98:21-4.
- Rollinson S, Richards S, Norfolk D, Bibi K, Morgan G, Hillmen P Both paroxysmal nocturnal hemoglobinuria (PNH) type II cells and PNH type III cells can arise from different point mutations involving the same codon of the PIG A gene. Blood 1997; 89:3069-71.
- Endo M, Ware RE, Vreeke TM, et al. Molecular basis of the heterogeneity of expression of glycosyl phosphatidylinositol anchored proteins in paroxysmal nocturnal hemoglobinuria. Blood 1996:87:2546–57.
- Nafa K, Bessler M, Deeg HJ, Luzzatto L, New somatic mutation in the PIG-A gene emerges at relapse of paroxysmal nocturnal hemoglobinuria. Blood 1998; 92:3422–7.
- Nafa K, Bessler M., Castro-Malaspina H, Jhanwar S, Luzzatto L. The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemogiobinuria includes large deletions and small duplications. Blood Cells Mol Dis 1998;24:370–84.
- Ham TH. Studies on destruction of red blood cells. I. Chronic hemolytic anemia with paroxysmal hemoglobinuria: an investigation of the mechanism of hemolysis, with observations on five cases. Archives of Internal Medicine 1939;64:1271.
- Ham TH, Dingle JH. 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; 18:657–72.
- Crookston JH, Crookston MC, Rosse WE Red-cell abnormalities in HEMPAS (hereditary erythroblastic multinuclearity with a positive acidified-serum test). Br J Haematol 1972;23 (Suppl):83–91.
- Dacie JV. Haemolytic anaemias. Vol, 5. Drug and chemical induced haemolytic anaemias; paroyxsmal noctural haemoglobinuria; haemolytic disease of the newborn. London: Churchill Livingstone, 1999.
- May JE, Rosse W, Frank MM, Paroxysmal nocturnal hemoglobinuria. Alternate-complement-pathway-mediated lysis induced by magnesium. N Engl J Med 1973;289:705-9.
- Hartmann RC, Jenkins DE. The “sugar-water” test for paroxysmal nocturnal hemoglobinuria. N Engl J Med 1966;275:155-7.
- Hartmann RC, Jenkins DE Jr, Arnold AB. Diagnostic specificity of sucrose hemolysis test for paroxysmal nocturnal hemoglobinuria. Blood 1970;35:462-75.
- Gotze O, Muller-Eberhard HJ. Paroxysmal nocturnal hemoglobinuria. Hemolysis initiated by the C3 activator system. N Engl J Med 1972;286:180-4.
- Kabakci T, Rosse WF, Logue GL. The lysis of paroxysmal nocturnal haemoglobinuria red cells by serum and cobra factor. Br J Haematol 1972;23:693-705.
- Hall SE, Rosse WE The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria. Blood 1996;87:5332–40.
- Navenot JM, Bernard D, Harousseau JL, Muller JY, Blanchard D, Expression of glycosyl-phosphatidylinositol-linked glycoproteins in blood cells from paroxysmal nocturnal haemoglobinuria patients—a flow cytometry study using CD55, CD58 and CD59 monoclonal antibodies. Leuk Lymphoma 1996; 21:143–51.
- Meletis J, Michali E, Samarkos M, et al. Detection of “PNH red cell” populations in hematological disorders using the Sephacryl Gel Test micro typing system. leuk Lymphoma 1997:28:177–82.
- Nilsson B, Hagström U, England A, Säfwenberg J. A simplified assay for the specific diagnosis of paroxysmal nocturnal hemoglobinuria: detection of DAF(CD55)- and HRF20(CD59)-erythrocytes in microtyping cards. Vox Sang 1993;64:43-6.
- Brodsky RA, Mukhina GL, Nelson KL, Lawrence TS, Jones RJ, Buckley JT. Resistance of paroxysmal nocturnal hemoglobinnria cells to the glycosylphosphatidylinositol-binding toxin aerolysin. Blood 1999;93:1749–56.
- McMullin MF, Hillmen P, Jackson J, Ganly P, Luzzatto L. Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuria. J Intern Med 1994;235:85–9.
- Sloand EM, Maciejewski JP, Dunn D, et al. Correction of the PNH defect by GPl-anchored protein transfer. Blood 1998;92:4439–45.