Schubert J, Vogt HG, Zielinska-Skowronek M, et al. Development of the glycosylphosphatidylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia. Blood 1994;83:2323-8.10.1182/blood.V83.8.2323.2323Search in Google Scholar
Griscelli-Bennaceur A, Gluckman E, Scrobohaci ML, et al. Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic link. Blood 1995;85:1354-63.10.1182/blood.V85.5.1354.bloodjournal8551354Search in Google Scholar
Hillmen P, Lewis SM, Bessler M, Luzzatto L, Dacie JV. Natural history of paroxysmal nocturnal hemoglobinuria. N Engl J Med 1995;333:1253-8.10.1056/NEJM199511093331904Search in Google Scholar
Socie G, Mary JY, Gramont A, et al. Paroxysmal nocturnal haemoglobinuria: long-term follow-up and prognostic factors. Lancet 1996;348:573-7.10.1016/S0140-6736(95)12360-1Search in Google Scholar
Zupanska B, Bogdanik I, Fabijanska-Mitek J, Pyl H. Autoimmune haemolytic anaemia with a paroxysmal nocturnal haemoglobinuria-like defect. Eur J Haematol 1999;62:346-9.10.1111/j.1600-0609.1999.tb01914.xSearch in Google Scholar
Rosse WF. Phosphatidylinositol-linked proteins and paroxysmal nocturnal hemoglobinuria. Blood 1990;75:1595-1601.10.1182/blood.V75.8.1595.1595Search in Google Scholar
Wilcox LA, Ezzell JL, Bernshaw NJ, Parker ChJ. Molecular basis of the enhanced susceptibility of the erythrocytes of paroxysmal nocturnal hemoglobinuria to hemolysis in acidified serum. Blood 1991;78:820-9.10.1182/blood.V78.3.820.820Search in Google Scholar
Yomtovian R, Prince GM, Medof ME. The molecular basis for paroxysmal nocturnal hemoglobinuria. Transfusion 1993;33:852-73.10.1046/j.1537-2995.1993.331094054626.xSearch in Google Scholar
Miyata T, Takeda J, Iida Y, et al. Cloning of PIG-A, a component in the early step of PGI-anchor biosynthesis. Science 1993;259:1318-20.10.1126/science.7680492Search in Google Scholar
Nishimura JI,Smith CA, Phillips KL, Warere EW, Rosse WF. Paroxysmal nocturnal hemoglobinuria: Molecular pathogenesis and molecular therapeutic approaches. Hematopathol Molecular Hematol 1998;11:119-46.Search in Google Scholar
Navenot JM, Bernard D, Petit-Frioux Y, et al. Diagnostic rapide des hemoglobinuries nocturnes paroxystiques par agglutination en gel. Rev Fr Transfus Hemobiol 1993;36:135-47.10.1016/S1140-4639(05)80230-8Search in Google Scholar
Nilsson B, Hagstrom U, Englund A, Safwenberg 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.Search in Google Scholar
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. Leukemia Lymphoma 1997;28:177-8210.3109/104281997090583449498717Search in Google Scholar
Beutler E. Sucrose hemolysis and acidified-serum lysis test. In: Williams Hematology. McGraw-Hill, Inc., 1995;L48-L49.Search in Google Scholar
Schubert J, Alvarado M, Uciechowski P, et al. Diagnosis of paroxysmal nocturnal haemoglo-binuria using immunophenotyping of peripheral blood cells. Br J Haematol 1991;79:487-92.10.1111/j.1365-2141.1991.tb08060.x1751377Search in Google Scholar
Bogdanik I, Pyl H, Zupanska B, Robak T. Flow cytometric analysis of erythrocyte and granulocyte defects in patients with paroxysmal nocturnal hemoglobinuria. Acta Haematologica Polonica 1998;29:69-75.Search in Google Scholar
van der Schoot CE, Huizinga TWJ, van t’Veer-Korthof ET, Wijams R, Pinkster J, von dem Borne AEGKr. Deficiency of glycosyl-phosphatidylinositol-linked membrane glycoproteins of leukocytes in paroxysmal nocturnal haemoglobinuria; description of a new diagnostic cytofluorometric assay. Blood 1990;76:1853-9.10.1182/blood.V76.9.1853.1853Search in Google Scholar
Marilyn B, Telen J, Green AM. The Inab phenotype: characterization of the membrane protein and complement regulatory defect. Blood 1989;74:437-41.10.1182/blood.V74.1.437.437Search in Google Scholar
