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Volumn 333, Issue 19, 1995, Pages 1253-1259

Natural history of paroxysmal nocturnal hemoglobinuria

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ANTICOAGULANT THERAPY; ARTICLE; BONE MARROW TRANSPLANTATION; CAUSE OF DEATH; DISEASE COURSE; FLOW CYTOMETRY; HUMAN; HUMAN TISSUE; INTRAVASCULAR HEMOLYSIS; LYMPHOCYTE; MAJOR CLINICAL STUDY; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PRIORITY JOURNAL; REMISSION; SOMATIC MUTATION; SURVIVAL; THROMBOCYTE TRANSFUSION; VEIN THROMBOSIS;

EID: 0028802443     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJM199511093331904     Document Type: Article
Times cited : (725)

References (40)
  • 2
    • 0000035046 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria
    • Dacie JV Paroxysmal nocturnal haemoglobinuria. Proc R Soc Med 1963; 56: 587-596
    • (1963) Proc R Soc Med , vol.56 , pp. 587-596
    • Dacie, J.1
  • 3
    • 0014832992 scopus 로고
    • Paroxysmal nocturnal hemoglobinuria: evidence for monoclonal origin of abnormal red cells
    • Oni SB, Osunkoya BO, Luzzatto L Paroxysmal nocturnal hemoglobinuria: evidence for monoclonal origin of abnormal red cells. Blood 1970; 36: 145-152
    • (1970) Blood , vol.36 , pp. 145-152
    • Oni, S.1    Osunkoya, B.2    Luzzatto, L.3
  • 4
    • 0026856908 scopus 로고
    • Glycosyl-phosphatidylinositol membrane anchors: the tale of a tail
    • Ferguson MAJ Glycosyl-phosphatidylinositol membrane anchors: the tale of a tail. Biochem Soc Trans 1992; 20: 243-256
    • (1992) Biochem Soc Trans , vol.20 , pp. 243-256
    • Ferguson, M.1
  • 5
    • 0025264867 scopus 로고
    • Phosphatidylinositol-linked proteins and paroxysmal nocturnal hemoglobinuria
    • Rosse WF Phosphatidylinositol-linked proteins and paroxysmal nocturnal hemoglobinuria. Blood 1990; 75: 1595-1601
    • (1990) Blood , vol.75 , pp. 1595-1601
    • Rosse, W.1
  • 6
    • 0000579387 scopus 로고
    • Paroxysmal nocturnal hemoglobinuria: a classic description by Paul StrãƒÂ¼bing in 1882, and a bibliography of the disease
    • Crosby WH Paroxysmal nocturnal hemoglobinuria: a classic description by Paul StrãƒÂ¼bing in 1882, and a bibliography of the disease. Blood 1951; 6: 270-284
    • (1951) Blood , vol.6 , pp. 270-284
    • Crosby, W.1
  • 7
    • 0025784355 scopus 로고
    • Dr. Ham's test revisited
    • Rosse WF Dr. Ham's test revisited. Blood 1991; 78: 547-550
    • (1991) Blood , vol.78 , pp. 547-550
    • Rosse, W.1
  • 8
    • 0024411828 scopus 로고
    • Isolation and characterization of a membrane protein from normal human erythrocytes that inhibits reactive lysis of the erythrocytes of paroxysmal nocturnal hemoglobinuria
    • Holguin MH, Fredrick LR, Bernshaw NJ, Wilcox LA, Parker CJ Isolation and characterization of a membrane protein from normal human erythrocytes that inhibits reactive lysis of the erythrocytes of paroxysmal nocturnal hemoglobinuria. J Clin Invest 1989; 84: 7-17
    • (1989) J Clin Invest , vol.84 , pp. 7
    • Holguin, M.1    Fredrick, L.2    Bernshaw, N.3    Wilcox, L.4    Parker, C.5
  • 9
    • 0025053264 scopus 로고
    • Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria
    • Yamashina M, Ueda E, Kinoshita T, Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria. N Engl J Med 1990; 323: 1184-1189
    • (1990) N Engl J Med , vol.323 , pp. 1184-1189
    • Yamashina, M.1    Ueda, E.2    Kinoshita, T.3
  • 10
    • 0026465067 scopus 로고
    • Affected paroxysmal nocturnal hemoglobinuria T lymphocytes harbor a common defect in assembly of N-acetyl-D-glucosamine inositol phospholipid corresponding to that in class A Thy-1- murine lymphoma mutants
    • Armstrong C, Schubert J, Ueda E, Affected paroxysmal nocturnal hemoglobinuria T lymphocytes harbor a common defect in assembly of N-acetyl-D-glucosamine inositol phospholipid corresponding to that in class A Thy-1- murine lymphoma mutants. J Biol Chem 1992; 267: 25347-25351
    • (1992) J Biol Chem , vol.267 , pp. 25347-25351
    • Armstrong, C.1    Schubert, J.2    Ueda, E.3
  • 11
    • 0027198876 scopus 로고
    • Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuria
    • Hillmen P, Bessler M, Mason PJ, Watkins WM, Luzzatto L Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuria. Proc Natl Acad Sci U S A 1993; 90: 5272-5276
    • (1993) Proc Natl Acad Sci U S A , vol.90 , pp. 5272-5276
    • Hillmen, P.1    Bessler, M.2    Mason, P.3    Watkins, W.4    Luzzatto, L.5
  • 12
    • 0027412005 scopus 로고
    • Deficient biosynthesis of N-acetylglucosaminyl-phosphatidylinositol, the first intermediate of glycosyl phosphatidylinositol anchor biosynthesis, in cell lines established from patients with paroxysmal nocturnal hemoglobinuria
    • Takahashi M, Takeda J, Hirose S, Deficient biosynthesis of N-acetylglucosaminyl-phosphatidylinositol, the first intermediate of glycosyl phosphatidylinositol anchor biosynthesis, in cell lines established from patients with paroxysmal nocturnal hemoglobinuria. J Exp Med 1993; 177: 517-521
    • (1993) J Exp Med , vol.177 , pp. 517-521
    • Takahashi, M.1    Takeda, J.2    Hirose, S.3
  • 13
    • 0027412627 scopus 로고
    • The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis
    • Miyata T, Takeda J, Iida Y, The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis. Science 1993; 259: 1318-1320
    • (1993) Science , vol.259 , pp. 1318-1320
    • Miyata, T.1    Takeda, J.2    Iida, Y.3
  • 14
    • 0027310539 scopus 로고
    • Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
    • Takeda J, Miyata T, Kawagoe K, Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell 1993; 73: 703-711
    • (1993) Cell , vol.73 , pp. 703-711
    • Takeda, J.1    Miyata, T.2    Kawagoe, K.3
  • 15
    • 0028057807 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene
    • Bessler M, Mason PJ, Hillmen P, Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. EMBO J 1994; 13: 110-117
    • (1994) EMBO J , vol.13 , pp. 110-117
    • Bessler, M.1    Mason, P.2    Hillmen, P.3
  • 16
    • 0028057618 scopus 로고
    • Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria
    • Miyata T, Yamada N, Iida Y, Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria. N Engl J Med 1994; 330: 249-255
    • (1994) N Engl J Med , vol.330 , pp. 249-255
    • Miyata, T.1    Yamada, N.2    Iida, Y.3
  • 17
    • 0028299834 scopus 로고
    • Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
    • Bessler M, Mason PJ, Hillmen P, Luzzatto L Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria. Lancet 1994; 343: 951-953
    • (1994) Lancet , vol.343 , pp. 951-953
    • Bessler, M.1    Mason, P.2    Hillmen, P.3    Luzzatto, L.4
  • 18
    • 0015863422 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria and refractory marrow failure treated by marrow transplantation
    • Storb R, Evans RS, Thomas ED, Paroxysmal nocturnal haemoglobinuria and refractory marrow failure treated by marrow transplantation. Br J Haematol 1973; 24: 743-750
    • (1973) Br J Haematol , vol.24 , pp. 743-750
    • Storb, R.1    Evans, R.2    Thomas, E.3
  • 19
    • 0026588963 scopus 로고
    • Marrow transplantation for paroxysmal nocturnal hemoglobinuria
    • Kawahara K, Witherspoon RP, Storb R Marrow transplantation for paroxysmal nocturnal hemoglobinuria. Am J Hematol 1992; 39: 283-288
    • (1992) Am J Hematol , vol.39 , pp. 283-288
    • Kawahara, K.1    Witherspoon, R.2    Storb, R.3
  • 20
    • 0028779536 scopus 로고
    • Bone marrow transplantation
    • Armitage JO Bone marrow transplantation. N Engl J Med 1994; 330: 827-838
    • (1994) N Engl J Med , vol.330 , pp. 827-838
    • Armitage, J.1
  • 21
    • 0001877267 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria
    • In: Dacie JV, Lewis SM, eds. Practical haematology. 8th ed. Edinburgh, Scotland: Churchill Livingstone,
    • Luzzatto L, Hillmen P. Paroxysmal nocturnal haemoglobinuria. In: Dacie JV, Lewis SM, eds. Practical haematology. 8th ed. Edinburgh, Scotland: Churchill Livingstone, 1995:287-96.
    • (1995) , pp. 287-296
    • Luzzatto, L.1    Hillmen, P.2
  • 22
    • 0015457605 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria: clinical manifestations, haematology, and nature of the disease
    • Dacie JV, Lewis SM Paroxysmal nocturnal haemoglobinuria: clinical manifestations, haematology, and nature of the disease. Ser Haematol 1972; 5: 3-23
    • (1972) Ser Haematol , vol.5 , pp. 3
    • Dacie, J.1    Lewis, S.2
  • 23
    • 0026537310 scopus 로고
    • Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency in the red cells of patients with paroxysmal nocturnal haemoglobinuria
    • Hillmen P, Hows JM, Luzzatto L Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency in the red cells of patients with paroxysmal nocturnal haemoglobinuria. Br J Haematol 1992; 80: 399-405
    • (1992) Br J Haematol , vol.80 , pp. 399-405
    • Hillmen, P.1    Hows, J.2    Luzzatto, L.3
  • 24
    • 0027492039 scopus 로고
    • Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotype
    • Hillmen P, Bessler M, Crawford DH, Luzzatto L Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotype. Blood 1993; 81: 193-199
    • (1993) Blood , vol.81 , pp. 193-199
    • Hillmen, P.1    Bessler, M.2    Crawford, D.3    Luzzatto, L.4
  • 25
    • 0001082037 scopus 로고
    • Paroxysmal nocturnal hemoglobinuria: relation of the clinical manifestations to underlying pathogenic mechanisms
    • Crosby WH Paroxysmal nocturnal hemoglobinuria: relation of the clinical manifestations to underlying pathogenic mechanisms. Blood 1953; 8: 769-812
    • (1953) Blood , vol.8 , pp. 769-812
    • Crosby, W.1
  • 26
    • 85023418334 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria
    • In: Dacie JV. The haemolytic anaemias. London: J&A Churchill
    • Paroxysmal nocturnal haemoglobinuria. In: Dacie JV. The haemolytic anaemias. London: J&A Churchill, 1954:412-50.
    • (1954) , pp. 412-450
  • 27
    • 0014528928 scopus 로고
    • Prolonged survival in paroxysmal nocturnal hemoglobinuria
    • Charache S Prolonged survival in paroxysmal nocturnal hemoglobinuria. Blood 1969; 33: 877-883
    • (1969) Blood , vol.33 , pp. 877-883
    • Charache, S.1
  • 28
    • 0019268572 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria
    • Dacie J Paroxysmal nocturnal haemoglobinuria. Sangre (Barc) 1980; 25: 890-895
    • (1980) Sangre (Barc) , vol.25 , pp. 890-895
    • Dacie, J.1
  • 29
    • 0001509253 scopus 로고
    • Refractory anaemia (Fanconi type)
    • Dacie JV, Gilpin A Refractory anaemia (Fanconi type). Arch Dis Child 1944; 19: 155-162
    • (1944) Arch Dis Child , vol.19 , pp. 155-162
    • Dacie, J.1    Gilpin, A.2
  • 30
    • 0343093975 scopus 로고
    • Possible paroxysmal nocturnal hemoglobinuria with pronounced pancytopenia, reticulocytopenia, and without hemoglobinuria simulating aplastic anemia
    • Letman H Possible paroxysmal nocturnal hemoglobinuria with pronounced pancytopenia, reticulocytopenia, and without hemoglobinuria simulating aplastic anemia. Blood 1952; 7: 842-849
    • (1952) Blood , vol.7 , pp. 842-849
    • Letman, H.1
  • 31
    • 78651129366 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria: variation in clinical severity and association with bone-marrow hypoplasia
    • Dacie JV, Lewis SM Paroxysmal nocturnal haemoglobinuria: variation in clinical severity and association with bone-marrow hypoplasia. Br J Haematol 1961; 7: 442-457
    • (1961) Br J Haematol , vol.7 , pp. 442-457
    • Dacie, J.1    Lewis, S.2
  • 32
    • 0019990451 scopus 로고
    • Decreased number of circulating BFU-Es in paroxysmal nocturnal hemoglobinuria
    • Rotoli B, Robledo R, Luzzatto L Decreased number of circulating BFU-Es in paroxysmal nocturnal hemoglobinuria. Blood 1982; 60: 157-159
    • (1982) Blood , vol.60 , pp. 157-159
    • Rotoli, B.1    Robledo, R.2    Luzzatto, L.3
  • 33
    • 0022570411 scopus 로고
    • Characterization of the hematopoietic defect in paroxysmal nocturnal hemoglobinuria
    • Moore JG, Humphries RK, Frank MM, Young N Characterization of the hematopoietic defect in paroxysmal nocturnal hemoglobinuria. Exp Hematol 1986; 14: 222-229
    • (1986) Exp Hematol , vol.14 , pp. 222-229
    • Moore, J.1    Humphries, R.2    Frank, M.3    Young, N.4
  • 34
    • 0015097760 scopus 로고
    • In vitro granulocytic colony-forming potential of bone marrow from patients with granulocytopenia and aplastic anaemia
    • Kurnick JE, Robinson WA, Dickey CA In vitro granulocytic colony-forming potential of bone marrow from patients with granulocytopenia and aplastic anaemia. Proc Soc Exp Med 1971; 137: 917-920
    • (1971) Proc Soc Exp Med , vol.137 , pp. 917-920
    • Kurnick, J.1    Robinson, W.2    Dickey, C.3
  • 36
    • 0024325872 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria
    • Rotoli B, Luzzatto L Paroxysmal nocturnal haemoglobinuria. Semin Hematol 1989; 26: 201-207
    • (1989) Semin Hematol , vol.26 , pp. 201-207
    • Rotoli, B.1    Luzzatto, L.2
  • 37
    • 0023104647 scopus 로고
    • Acute myeloblastic leukemia in paroxysmal nocturnal hemoglobinuria: evidence of evolution from the abnormal paroxysmal nocturnal hemoglobinuria clone
    • Devine DV, Gluck WL, Rosse WF, Weinberg JB Acute myeloblastic leukemia in paroxysmal nocturnal hemoglobinuria: evidence of evolution from the abnormal paroxysmal nocturnal hemoglobinuria clone. J Clin Invest 1987; 79: 314-317
    • (1987) J Clin Invest , vol.79 , pp. 314-317
    • Devine, D.1    Gluck, W.2    Rosse, W.3    Weinberg, J.4
  • 38
    • 0028234052 scopus 로고
    • Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease
    • Longo L, Bessler M, Beris P, Swirsky D, Luzzatto L Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease. Br J Haematol 1994; 87: 401-403
    • (1994) Br J Haematol , vol.87 , pp. 401-403
    • Longo, L.1    Bessler, M.2    Beris, P.3    Swirsky, D.4    Luzzatto, L.5
  • 39
    • 0028229227 scopus 로고
    • Myelodysplasia following paroxysmal nocturnal haemoglobinuria: evidence for the emergence of a separate clone
    • van Kamp H, Smit JW, van den Berg E, Halie MR, Vellenga E Myelodysplasia following paroxysmal nocturnal haemoglobinuria: evidence for the emergence of a separate clone. Br J Haematol 1994; 87: 399-400
    • (1994) Br J Haematol , vol.87 , pp. 399-400
    • van Kamp, H.1    Smit, J.2    van den Berg, E.3    Halie, M.R.4    Vellenga, E.5
  • 40
    • 0028275515 scopus 로고
    • Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuria
    • 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: 85-89
    • (1994) J Intern Med , vol.235 , pp. 85-89
    • McMullin, M.1    Hillmen, P.2    Jackson, J.3    Ganly, P.4    Luzzatto, L.5


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