-
1
-
-
0014832992
-
Paroxysmal nocturnal hemoglobinuria: Evidence for monoclonal origin of abnormal red cells
-
Oni S, Osunkoya B, 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
-
2
-
-
0001802499
-
Hemolysis in PNH
-
Young NS, Moss J (eds). Academic Press: San Diego
-
Parker CJ. Hemolysis in PNH. In: Young NS, Moss J (eds). PNH and the GPI-linked Proteins. Academic Press: San Diego, 2000, pp. 49-100.
-
(2000)
PNH and the GPI-linked Proteins
, pp. 49-100
-
-
Parker, C.J.1
-
3
-
-
0028884057
-
The molecular basis of paroxysmal nocturnal hemoglobinuria
-
Rosse WF, Ware R. The molecular basis of paroxysmal nocturnal hemoglobinuria. Blood 1995; 9: 3277-3286.
-
(1995)
Blood
, vol.9
, pp. 3277-3286
-
-
Rosse, W.F.1
Ware, R.2
-
4
-
-
0033974579
-
The molecular basis of paroxysmal nocturnal hemoglobinuria
-
Rosti V. The molecular basis of paroxysmal nocturnal hemoglobinuria. Haematologica 2000; 85: 82-87.
-
(2000)
Haematologica
, vol.85
, pp. 82-87
-
-
Rosti, V.1
-
5
-
-
0027412627
-
The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis
-
Miyata T, Takeda J, Iida Y, Yamada N, Inoue N, Takahashi M. Maeda K, Kitani T, Kinoshita T. The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis. Science 1993; 2591: 318-320.
-
(1993)
Science
, vol.2591
, pp. 318-320
-
-
Miyata, T.1
Takeda, J.2
Iida, Y.3
Yamada, N.4
Inoue, N.5
Takahashi, M.6
Maeda, K.7
Kitani, T.8
Kinoshita, T.9
-
6
-
-
0027198876
-
Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphaticylinositol 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 glycosylphosphaticylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuria. Proc Natl Acad Sci USA 1993; 90: 5272-5276.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 5272-5276
-
-
Hillmen, P.1
Bessler, M.2
Mason, P.J.3
Watkins, W.M.4
Luzzatto, L.5
-
7
-
-
0028057618
-
Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria
-
Miyata T, Yamada N, Iida Y, Nishimura J, Takeda J, Kitani T, Kinoshita T. 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
Nishimura, J.4
Takeda, J.5
Kitani, T.6
Kinoshita, T.7
-
8
-
-
0033609114
-
Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals
-
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: 5209-5214.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 5209-5214
-
-
Araten, D.J.1
Nafa, K.2
Pakdeesuwan, K.3
Luzzatto, L.4
-
9
-
-
0015457605
-
Paroxysmal nocturnal hemoglobinuria; clinical manifestations, haematology, and nature of the disease. 1
-
Dacie JV, Lewis SM. Paroxysmal nocturnal hemoglobinuria; clinical manifestations, haematology, and nature of the disease. 1. Series Haematologica 1972; 5: 2-23.
-
(1972)
Series Haematologica
, vol.5
, pp. 2-23
-
-
Dacie, J.V.1
Lewis, S.M.2
-
10
-
-
0011447889
-
Paroxysmal nocturnal hemoglobinuria
-
Young, NS (ed). WB Saunders: Philadelphia
-
Dunn DE, Liu JM, Young NS. Paroxysmal nocturnal hemoglobinuria. In: Young, NS (ed). Bone Marrow Failure Syndromes. WB Saunders: Philadelphia, 2000, pp. 99-121.
-
(2000)
Bone Marrow Failure Syndromes
, pp. 99-121
-
-
Dunn, D.E.1
Liu, J.M.2
Young, N.S.3
-
11
-
-
0030932540
-
Somatic mutations in paroxysmal nocturnal hemoglobinuria: A blessing in disguise?
-
Luzzatto L, Bessler M, Rotoli B. Somatic mutations in paroxysmal nocturnal hemoglobinuria: a blessing in disguise? Cell 1997; 88: 1-4.
-
(1997)
Cell
, vol.88
, pp. 1-4
-
-
Luzzatto, L.1
Bessler, M.2
Rotoli, B.3
-
13
-
-
0026596863
-
The problem of clonality in aplastic anemia: Dr Dameshek's riddle restated
-
Young NS. The problem of clonality in aplastic anemia: Dr Dameshek's riddle restated. Blood 1992; 79: 1385-1392.
-
(1992)
Blood
, vol.79
, pp. 1385-1392
-
-
Young, N.S.1
-
14
-
-
0019990451
-
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
-
15
-
-
0029933457
-
Correction of aplastic anemia complicating paroxysmal nocturnal hemoglobinuria: Absence of eradication of the PNH clone and dependence of response on cyclosporin A administration
-
Stoppa AM, Vey N, Sainty D, Arnoulet C, Camerlo J, Cappiello MA, Gastaut JA, Maraninchi D. Correction of aplastic anemia complicating paroxysmal nocturnal hemoglobinuria: absence of eradication of the PNH clone and dependence of response on cyclosporin A administration. Br J Haematol 1996; 93: 42-44.
-
(1996)
Br. J. Haematol
, vol.93
, pp. 42-44
-
-
Stoppa, A.M.1
Vey, N.2
Sainty, D.3
Arnoulet, C.4
Camerlo, J.5
Cappiello, M.A.6
Gastaut, J.A.7
Maraninchi, D.8
-
16
-
-
0034307521
-
Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuria
-
Karadimitris A, Manavalan JS, Thaler HT, Notaro, R. Araten DJ, Nafa K. Roberts IA, Weksler ME, Luzzatto L. Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuria. Blood 2000; 96: 2613-2620.
-
(2000)
Blood
, vol.96
, pp. 2613-2620
-
-
Karadimitris, A.1
Manavalan, J.S.2
Thaler, H.T.3
Notaro, R.4
Araten, D.J.5
Nafa, K.6
Roberts, I.A.7
Weksler, M.E.8
Luzzatto, L.9
-
17
-
-
0035726553
-
Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria
-
Araten DJ, Swirsky D, Karadimitris A, Notaro R. Nafa K, Bessler M, Thaler HT, Castro-Malaspina H, Childs BH, Boulad F, Weiss M, Anagnostopoulos N, Kutlar A, Savage DG, Maziarz RT, Jhanwar S, Luzzatto L. Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria. Br J Haematol 2001; 115: 360-368.
-
(2001)
Br. J. Haematol
, vol.115
, pp. 360-368
-
-
Araten, D.J.1
Swirsky, D.2
Karadimitris, A.3
Notaro, R.4
Nafa, K.5
Bessler, M.6
Thaler, H.T.7
Castro-Malaspina, H.8
Childs, B.H.9
Boulad, F.10
Weiss, M.11
Anagnostopoulos, N.12
Kutlar, A.13
Savage, D.G.14
Maziarz, R.T.15
Jhanwar, S.16
Luzzatto, L.17
-
18
-
-
0033592318
-
Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes
-
Dunn DE, Tanawattanacharoen P, Boccuni P, Nagakura S, Green SW, Kirby MR, Kumar MS, Rosenfeld S, Young NS. Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes. Ann Intem Med 1999; 131: 401-408.
-
(1999)
Ann. Intem. Med
, vol.131
, pp. 401-408
-
-
Dunn, D.E.1
Tanawattanacharoen, P.2
Boccuni, P.3
Nagakura, S.4
Green, S.W.5
Kirby, M.R.6
Kumar, M.S.7
Rosenfeld, S.8
Young, N.S.9
-
19
-
-
0031822254
-
Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes
-
Iwanaga M, Furukawa K, Amenomori T, Mori H. Nakamura H, Fuchigami K, Kamihira S, Nakakuma H, Tomonaga M. Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes. Br J Haematol 1998; 102: 465-474.
-
(1998)
Br. J. Haematol
, vol.102
, pp. 465-474
-
-
Iwanaga, M.1
Furukawa, K.2
Amenomori, T.3
Mori, H.4
Nakamura, H.5
Fuchigami, K.6
Kamihira, S.7
Nakakuma, H.8
Tomonaga, M.9
-
20
-
-
0032980348
-
Leukemia arising out of paroxysmal nocturnal hemoglobinuria
-
Harris JW, Koscick R, Lazarus HM, Eshleman JR, Medof ME. Leukemia arising out of paroxysmal nocturnal hemoglobinuria. Leuk Lymphoma 1999; 32: 401-426.
-
(1999)
Leuk. Lymphoma
, vol.32
, pp. 401-426
-
-
Harris, J.W.1
Koscick, R.2
Lazarus, H.M.3
Eshleman, J.R.4
Medof, M.E.5
-
21
-
-
0034084440
-
Prolonged response to cyclosporin-A in hypoplastic refractory anemia and correlation with in vitro studies
-
Catalano L, Selleri C, Califano C, Luciano L, Volpicelli M, Rocco S, Varriale G, Ricci P, Rotoli B. Prolonged response to cyclosporin-A in hypoplastic refractory anemia and correlation with in vitro studies. Haematologica 2000; 85: 133-138.
-
(2000)
Haematologica
, vol.85
, pp. 133-138
-
-
Catalano, L.1
Selleri, C.2
Califano, C.3
Luciano, L.4
Volpicelli, M.5
Rocco, S.6
Varriale, G.7
Ricci, P.8
Rotoli, B.9
-
22
-
-
0035673563
-
Relationship between bone marrow failure syndromes and the presence of glycosylphosphatidyl inositol-anchored protein-deficient clones
-
Maciejewski JP, Rivera C, Kook H, Dunn D, Young NS. Relationship between bone marrow failure syndromes and the presence of glycosylphosphatidyl inositol-anchored protein-deficient clones. Br J Haematol. 2001; 115: 1015-1022.
-
(2001)
Br. J. Haematol
, vol.115
, pp. 1015-1022
-
-
Maciejewski, J.P.1
Rivera, C.2
Kook, H.3
Dunn, D.4
Young, N.S.5
-
23
-
-
0028802443
-
Natural history of paroxysmal nocturnal hemoglobinuria
-
Hillmen P, Lewis SM, Bessler M, Luzzatto L, Dacie JV. Natural history of paroxysmal nocturnal hemoglobinuria. N Engl J Med 1995; 33: 1253-1258.
-
(1995)
N. Engl. J. Med
, vol.33
, pp. 1253-1258
-
-
Hillmen, P.1
Lewis, S.M.2
Bessler, M.3
Luzzatto, L.4
Dacie, J.V.5
-
24
-
-
0029096416
-
Decay accelerating factor deficient erythrocytes during the long-term clinical course of patients with paroxysmal nocturnal hemoglobinuria
-
Mahbub B, Nishimura J, Kitani T, Kitano K. Decay accelerating factor deficient erythrocytes during the long-term clinical course of patients with paroxysmal nocturnal hemoglobinuria. Acta Haematol 1995; 93: 91-97.
-
(1995)
Acta Haematol
, vol.93
, pp. 91-97
-
-
Mahbub, B.1
Nishimura, J.2
Kitani, T.3
Kitano, K.4
-
25
-
-
0034096753
-
Paroxysmal nocturnal haemoglobinura: A replacement of haematopoietic tissue?
-
Schrezenmeier H, Hildebrand A, Rojewski M, Hacker H, HH, Raghavachar A. Paroxysmal nocturnal haemoglobinura: a replacement of haematopoietic tissue? Acta Haematol 2000; 103: 41-48.
-
(2000)
Acta Haematol
, vol.103
, pp. 41-48
-
-
Schrezenmeier, H.1
Hildebrand, A.2
Rojewski, M.3
Hacker, H.H.H.4
Raghavachar, A.5
-
26
-
-
0033813333
-
Detection of small populations of CD59-deficient erythrocytes in patients with aplastic anemia or myelodysplastic syndrome and normal individuals
-
Yamaguchi M, Machii T, Azenishi Y, Nishimura J, Shibano M, Kanakura Y, Kitani T. Detection of small populations of CD59-deficient erythrocytes in patients with aplastic anemia or myelodysplastic syndrome and normal individuals. Blood Cells Mol Dis. 2000; 26: 247-254.
-
(2000)
Blood Cells Mol. Dis
, vol.26
, pp. 247-254
-
-
Yamaguchi, M.1
Machii, T.2
Azenishi, Y.3
Nishimura, J.4
Shibano, M.5
Kanakura, Y.6
Kitani, T.7
-
27
-
-
0035058599
-
Relative increase of granulocytes with a paroxysmal nocturnal haemoglobinuria phenotype in aplastic anemia patients: The high prevalence at diagnosis
-
Wang H, Chuhjo T, Yamazaki H, Shiobara S, Teramura M, Mizoguchi H, Nakao S. Relative increase of granulocytes with a paroxysmal nocturnal haemoglobinuria phenotype in aplastic anemia patients: The high prevalence at diagnosis. Eur J Haematol 2001; 66: 200-205.
-
(2001)
Eur. J. Haematol
, vol.66
, pp. 200-205
-
-
Wang, H.1
Chuhjo, T.2
Yamazaki, H.3
Shiobara, S.4
Teramura, M.5
Mizoguchi, H.6
Nakao, S.7
-
28
-
-
0033230899
-
Paroxysmal murine hemoglobinuria (?): A model for human PNH
-
Luzzatto L. Paroxysmal murine hemoglobinuria (?): a model for human PNH. Blood 1999; 94: 2941-2944.
-
(1999)
Blood
, vol.94
, pp. 2941-2944
-
-
Luzzatto, L.1
-
29
-
-
0034882347
-
The cellular pathogeneisis of paroxysmal nocturnal haemoglobinuria
-
Karadimitris A, Luzzatto L. The cellular pathogeneisis of paroxysmal nocturnal haemoglobinuria. Leukemia 2001; I5: 1148-1152.
-
(2001)
Leukemia
, vol.15
, pp. 1148-1152
-
-
Karadimitris, A.1
Luzzatto, L.2
-
30
-
-
0028299834
-
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
-
Bessler M, Mason P, 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
-
31
-
-
0030942613
-
A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clones
-
Nishimura J, Inoue N, Wada H et al. A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clones. Blood 1997; 89: 3470-3476.
-
(1997)
Blood
, vol.89
, pp. 3470-3476
-
-
Nishimura, J.1
Inoue, N.2
Wada, H.3
-
32
-
-
0022410146
-
Bone marrow transplantation for paroxysmal nocturnal hemoglobinuria: Eradication of the PNH clone and documentation of complete lymphohematopoietic engraftment
-
Antin JH, Ginsburg D, Smith BR, Nathan DG, Orkin SH, Rappeport JM. Bone marrow transplantation for paroxysmal nocturnal hemoglobinuria: eradication of the PNH clone and documentation of complete lymphohematopoietic engraftment. Blood 1985; 66: 1247-1250.
-
(1985)
Blood
, vol.66
, pp. 1247-1250
-
-
Antin, J.H.1
Ginsburg, D.2
Smith, B.R.3
Nathan, D.G.4
Orkin, S.H.5
Rappeport, J.M.6
-
33
-
-
0031032545
-
Clinical characteristics predict response to anithymocyte globulin in paroxysmal nocturnal haemoglobinuria
-
Paquette RL, Yoshimura R, Veiseh C, Kunkel L, Gajewski J, Rosen PJ. Clinical characteristics predict response to anithymocyte globulin in paroxysmal nocturnal haemoglobinuria. Br J Haematol 1997; 96: 92-97.
-
(1997)
Br. J. Haematol
, vol.96
, pp. 92-97
-
-
Paquette, R.L.1
Yoshimura, R.2
Veiseh, C.3
Kunkel, L.4
Gajewski, J.5
Rosen, P.J.6
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