-
1
-
-
43049090537
-
Narrative review. Paroxysmal nocturnal hemoglobinuria: The physiology of complement-related hemolytic anemia
-
Brodsky RA. Narrative review. Paroxysmal nocturnal hemoglobinuria: the physiology of complement-related hemolytic anemia. Ann Intern Med. 2008;148:587-595.
-
(2008)
Ann Intern Med
, vol.148
, pp. 587-595
-
-
Brodsky, R.A.1
-
2
-
-
0036223611
-
Historical aspects of paroxysmal nocturnal haemoglobinuria: "defining the disease."
-
Parker CJ. Historical aspects of paroxysmal nocturnal haemoglobinuria: "defining the disease." Br J Haematol. 2002;117:3-22.
-
(2002)
Br J Haematol
, vol.117
, pp. 3-22
-
-
Parker, C.J.1
-
3
-
-
28444483571
-
Diagnosis and management of paroxysmal nocturnal hemoglobinuria
-
DOI 10.1182/blood-2005-04-1717
-
Parker C, Omine M, Richards S, et al. Diagnosis and management of paroxysmal nocturnal hemoglobinuria. Blood. 2005;106:3699-3709. (Pubitemid 41739003)
-
(2005)
Blood
, vol.106
, Issue.12
, pp. 3699-3709
-
-
Parker, C.1
Omine, M.2
Richards, S.3
Nishimura, J.-I.4
Bessler, M.5
Ware, R.6
Hillmen, P.7
Luzzatto, L.8
Young, N.9
Kinoshita, T.10
Rosse, W.11
Socie, G.12
-
4
-
-
0027412627
-
The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis
-
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;259:1318-1320. (Pubitemid 23100269)
-
(1993)
Science
, vol.259
, Issue.5099
, pp. 1318-1320
-
-
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
-
5
-
-
0028057618
-
Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria
-
DOI 10.1056/NEJM199401273300404
-
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;330:249-255. (Pubitemid 24034137)
-
(1994)
New England Journal of Medicine
, vol.330
, Issue.4
, pp. 249-255
-
-
Miyata, T.1
Yamada, N.2
Iida, Y.3
Nishimura, J.4
Takeda, J.5
Kitani, T.6
Kinoshita, T.7
-
6
-
-
0021713655
-
Inhibition of complement activation on the surface of cells after incorporation of decay-accelerating factor (DAF) into their membranes
-
DOI 10.1084/jem.160.5.1558
-
Medof ME, Kinoshita T, Nussenzweig V. Inhibition of complement activation on the surface of cells after incorporation of decay-accelerating factor (DAF) into their membranes. J Exp Med. 1984; 160:1558-1578. (Pubitemid 15220783)
-
(1984)
Journal of Experimental Medicine
, vol.160
, Issue.5
, pp. 1558-1578
-
-
Medof, M.E.1
Kinoshita, T.2
Nussenzweig, V.3
-
7
-
-
0025233715
-
The complement-inhibitory activity of CD59 resides in its capacity to block incorporation of C9 into membrane C5b-9
-
Rollins SA, Sims PJ. The complement-inhibitory activity of CD59 resides in its capacity to block incorporation of C9 into membrane C5b-9. J Immunol. 1990;144:3478-3483.
-
(1990)
J Immunol
, vol.144
, pp. 3478-3483
-
-
Rollins, S.A.1
Sims, P.J.2
-
8
-
-
15944398355
-
The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: A novel mechanism of human disease
-
DOI 10.1001/jama.293.13.1653
-
Rother RP, Bell L, Hillmen P, Gladwin MT. The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: a novel mechanism of human disease. JAMA. 2005;293:1653-1662. (Pubitemid 40471796)
-
(2005)
Journal of the American Medical Association
, vol.293
, Issue.13
, pp. 1653-1662
-
-
Rother, R.P.1
Bell, L.2
Hillmen, P.3
Gladwin, M.T.4
-
9
-
-
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;333:1253-1258.
-
(1995)
N Engl J Med
, vol.333
, pp. 1253-1258
-
-
Hillmen, P.1
Lewis, S.M.2
Bessler, M.3
Luzzatto, L.4
Dacie, J.V.5
-
10
-
-
54049098831
-
Paroxysmal nocturnal hemoglobinuria: Natural history of disease subcategories
-
de Latour RP, Mary JY, Salanoubat C, et al. Paroxysmal nocturnal hemoglobinuria: natural history of disease subcategories. Blood. 2008;112: 3099-3106.
-
(2008)
Blood
, vol.112
, pp. 3099-3106
-
-
De Latour, R.P.1
Mary, J.Y.2
Salanoubat, C.3
-
11
-
-
3042789125
-
Natural history of paroxysmal nocturnal hemoglobinuria using modern diagnostic assays
-
Moyo VM, Mukhina GL, Garrett ES, Brodsky RA. Natural history of paroxysmal nocturnal hemoglobinuria using modern diagnostic assays. Br J Haematol. 2004;126:133-138.
-
(2004)
Br J Haematol
, vol.126
, pp. 133-138
-
-
Moyo, V.M.1
Mukhina, G.L.2
Garrett, E.S.3
Brodsky, R.A.4
-
12
-
-
2442532784
-
Clinical course and flow cytometric analysis of paroxysmal nocturnal hemoglobinuria in the United States and Japan
-
DOI 10.1097/01.md.0000126763.68170.46
-
Nishimura J, Kanakura Y, Ware RE, et al. Clinical course and flow cytometric analysis of paroxysmal nocturnal hemoglobinuria in the United States and Japan. Medicine (Baltimore). 2004;83: 193-207. (Pubitemid 38649949)
-
(2004)
Medicine
, vol.83
, Issue.3
, pp. 193-207
-
-
Nishimura, J.-I.1
Kanakura, Y.2
Ware, R.E.3
Shichishima, T.4
Nakakuma, H.5
Ninomiya, H.6
Decastro, C.M.7
Hall, S.8
Kanamaru, A.9
Sullivan, K.M.10
Mizoguchi, H.11
Omine, M.12
Kinoshita, T.13
Rosse, W.F.14
-
13
-
-
0035724869
-
Multilineage glycosylphosphatidylinositol anchor deficient hematopoiesis in untreated aplastic anemia
-
Mukhina GL, Buckley JT, Barber JP, Jones RJ, Brodsky RA. Multilineage glycosylphosphatidylinositol anchor deficient hematopoiesis in untreated aplastic anemia. Br J Haematol. 2001; 115:476-482.
-
(2001)
Br J Haematol
, vol.115
, pp. 476-482
-
-
Mukhina, G.L.1
Buckley, J.T.2
Barber, J.P.3
Jones, R.J.4
Brodsky, R.A.5
-
14
-
-
0033592318
-
Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes
-
Dunn DE, Tanawattanacharoen P, Boccuni P, et al. Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes. Ann Intern Med. 1999;131:401-408. (Pubitemid 29444429)
-
(1999)
Annals of Internal Medicine
, vol.131
, Issue.6
, 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.A.7
Rosenfeld, S.8
Young, N.S.9
-
15
-
-
0035058599
-
Relative increase of granulocytes with a paroxysmal nocturnal haemoglobinuria phenotype in aplastic anaemia patients: The high prevalence at diagnosis
-
DOI 10.1034/j.1600-0609.2001.00376.x
-
Wang H, Chuhjo T, Yamazaki H, et al. Relative increase of granulocytes with a paroxysmal nocturnal haemoglobinuria phenotype in aplastic anaemia patients: the high prevalence at diagnosis. Eur J Haematol. 2001;66:200-205. (Pubitemid 32324587)
-
(2001)
European Journal of Haematology
, vol.66
, Issue.3
, pp. 200-205
-
-
Wang, H.1
Chuhjo, T.2
Yamazaki, H.3
Shiobara, S.4
Teramura, M.5
Mizoguchi, H.6
Nakao, S.7
-
17
-
-
33750628439
-
Current concepts in the pathophysiology and treatment of aplastic anemia
-
DOI 10.1182/blood-2006-03-010777
-
Young NS, Calado RT, Scheinberg P. Current concepts in the pathophysiology and treatment of aplastic anemia. Blood. 2006;108:2509-2519. (Pubitemid 44776983)
-
(2006)
Blood
, vol.108
, Issue.8
, pp. 2509-2519
-
-
Young, N.S.1
Calado, R.T.2
Scheinberg, P.3
-
18
-
-
0028802885
-
Genetic defects underlying paroxysmal nocturnal hemoglobinuria that arises out of aplastic anemia
-
Nagarajan S, Brodsky RA, Young NS, Medof ME. Genetic defects underlying paroxysmal nocturnal hemoglobinuria that arises out of aplastic anemia. Blood. 1995;86:4656-4661.
-
(1995)
Blood
, vol.86
, pp. 4656-4661
-
-
Nagarajan, S.1
Brodsky, R.A.2
Young, N.S.3
Medof, M.E.4
-
19
-
-
0001194004
-
Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria: A study of the mechanism of hemolysisin relation to acid-base equilibrium
-
Ham T. Chronic hemolytic anemia with paroxysmal nocturnal hemoglobinuria: a study of the mechanism of hemolysisin relation to acid-base equilibrium. N Engl J Med. 1937;217:915-917.
-
(1937)
N Engl J Med
, vol.217
, pp. 915-917
-
-
Ham, T.1
-
20
-
-
0014024266
-
The "sugar-water" test for paroxysmal nocturnal hemoglobinuria
-
Hartmann RC, Jenkins DE. The "sugar-water" test for paroxysmal nocturnal hemoglobinuria. N Engl J Med. 1966;275:155-157.
-
(1966)
N Engl J Med
, vol.275
, pp. 155-157
-
-
Hartmann, R.C.1
Jenkins, D.E.2
-
21
-
-
0013911413
-
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
-
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;45:736-748.
-
(1966)
J Clin Invest
, vol.45
, pp. 736-748
-
-
Rosse, W.F.1
Dacie, J.V.2
-
22
-
-
0025866225
-
Fc III receptors (FcRIII) on granulocytes: A specific and sensitive diagnostic test for paroxysmal nocturnal hemoglobinuria (PNH)
-
Bessler M, Fehr J. Fc III receptors (FcRIII) on granulocytes: a specific and sensitive diagnostic test for paroxysmal nocturnal hemoglobinuria (PNH). Eur J Haematol. 1991;47:179-184.
-
(1991)
Eur J Haematol
, vol.47
, pp. 179-184
-
-
Bessler, M.1
Fehr, J.2
-
23
-
-
0029981029
-
The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria
-
Hall SE, Rosse WF. The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria. Blood. 1996; 87:5332-5340. (Pubitemid 26189877)
-
(1996)
Blood
, vol.87
, Issue.12
, pp. 5332-5340
-
-
Hall, S.E.1
Rosse, W.F.2
-
24
-
-
0024333970
-
The Inab phenotype: Characterization of the membrane protein and complement regulatory defect
-
Telen MJ, Green AM. The Inab phenotype: characterization of the membrane protein and complement regulatory defect. Blood. 1989;74: 437-441.
-
(1989)
Blood
, vol.74
, pp. 437-441
-
-
Telen, M.J.1
Green, A.M.2
-
25
-
-
0025053264
-
Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria
-
Yamashina M, Ueda E, Kinoshita T, et al. 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. (Pubitemid 20347405)
-
(1990)
New England Journal of Medicine
, vol.323
, Issue.17
, pp. 1184-1189
-
-
Yamashina, M.1
Ueda, E.2
Kinoshita, T.3
Takami, T.4
Ojima, A.5
Ono, H.6
Tanaka, H.7
Kondo, N.8
Orii, T.9
Okada, N.10
Okada, H.11
Inoue, K.12
Kitani, T.13
-
26
-
-
0034502010
-
Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin
-
Brodsky RA, Mukhina GL, Li S, et al. Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin. Am J Clin Pathol. 2000;114:459-466. (Pubitemid 33049682)
-
(2000)
American Journal of Clinical Pathology
, vol.114
, Issue.3
, pp. 459-466
-
-
Brodsky, R.A.1
Mukhina, G.L.2
Li, S.3
Nelson, K.L.4
Chiurazzi, P.L.5
Buckley, J.T.6
Borowitz, M.J.7
-
27
-
-
0030043134
-
Aerolysin: The ins and outs of a model channel-forming toxin
-
Parker MW, van der Goot FG, Buckley JT. Aerolysin: the ins and outs of a model channel-forming toxin. Mol Microbiol. 1996;19:205-212.
-
(1996)
Mol Microbiol
, vol.19
, pp. 205-212
-
-
Parker, M.W.1
Van Der Goot, F.G.2
Buckley, J.T.3
-
28
-
-
0030978914
-
The glycosylphosphatidylinositol-anchored surface glycoprotein Thy-1 is a receptor for the channel-forming toxin aerolysin
-
DOI 10.1074/jbc.272.18.12170
-
Nelson KL, Raja SM, Buckley JT. The glycosylphosphatidylinositol-anchored surface glycoprotein Thy-1 is a receptor for the channelforming toxin aerolysin. J Biol Chem. 1997;272: 12170-12174. (Pubitemid 27202800)
-
(1997)
Journal of Biological Chemistry
, vol.272
, Issue.18
, pp. 12170-12174
-
-
Nelson, K.L.1
Raja, S.M.2
Buckley, J.T.3
-
29
-
-
0033105696
-
Resistance of paroxysmal nocturnal hemoglobinuria cells to the glycosylphosphatidylinositol-binding toxin aerolysin
-
Brodsky RA, Mukhina GL, Nelson KL, et al. Resistance of paroxysmal nocturnal hemoglobinuria cells to the glycosylphosphatidylinositol-binding toxin aerolysin. Blood. 1999;93:1749-1756. (Pubitemid 29102504)
-
(1999)
Blood
, vol.93
, Issue.5
, pp. 1749-1756
-
-
Brodsky, R.A.1
Mukhina, G.L.2
Nelson, K.L.3
Lawrence, T.S.4
Jones, R.J.5
Buckley, J.T.6
-
30
-
-
18544381754
-
PIG-A mutations in normal hematopoiesis
-
Hu R, Mukhina GL, Piantadosi S, et al. PIG-A mutations in normal hematopoiesis. Blood. 2005; 105:3848-3854.
-
(2005)
Blood
, vol.105
, pp. 3848-3854
-
-
Hu, R.1
Mukhina, G.L.2
Piantadosi, S.3
-
31
-
-
0033609114
-
Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals
-
DOI 10.1073/pnas.96.9.5209
-
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 U S A. 1999;96:5209-5214. (Pubitemid 29214562)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.9
, pp. 5209-5214
-
-
Araten, D.J.1
Nafa, K.2
Pakdeesuwan, K.3
Luzzatto, L.4
-
32
-
-
0035655579
-
Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes
-
Ware RE, Pickens CV, DeCastro CM, Howard TA. Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes. Exp Hematol. 2001;29:1403-1409.
-
(2001)
Exp Hematol
, vol.29
, pp. 1403-1409
-
-
Ware, R.E.1
Pickens, C.V.2
Decastro, C.M.3
Howard, T.A.4
-
33
-
-
37349071491
-
On the origin of multiple mutant clones in paroxysmal nocturnal hemoglobinuria
-
DOI 10.1634/stemcells.2007-0427
-
Traulsen A, Pacheco JM, Dingli D. On the origin of multiple mutant clones in paroxysmal nocturnal hemoglobinuria. Stem Cells. 2007;25:3081-3084. (Pubitemid 350294433)
-
(2007)
Stem Cells
, vol.25
, Issue.12
, pp. 3081-3084
-
-
Traulsen, A.1
Pacheco, J.M.2
Dingli, D.3
-
34
-
-
0036893544
-
Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome
-
DOI 10.1182/blood-2002-03-0799
-
Wang H, Chuhjo T, Yasue S, Omine M, Nakao S. Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome. Blood. 2002;100: 3897-3902. (Pubitemid 35396854)
-
(2002)
Blood
, vol.100
, Issue.12
, pp. 3897-3902
-
-
Wang, H.1
Chuhjo, T.2
Yasue, S.3
Omine, M.4
Nakao, S.5
-
35
-
-
33644505823
-
Quantitative analysis of bone marrow CD34 cells in aplastic anemia and hypoplastic myelodysplastic syndromes
-
Matsui WH, Brodsky RA, Smith BD, Borowitz MJ, Jones RJ. Quantitative analysis of bone marrow CD34 cells in aplastic anemia and hypoplastic myelodysplastic syndromes. Leukemia. 2006;20: 458-462.
-
(2006)
Leukemia
, vol.20
, pp. 458-462
-
-
Matsui, W.H.1
Brodsky, R.A.2
Smith, B.D.3
Borowitz, M.J.4
Jones, R.J.5
-
36
-
-
35948959015
-
Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria
-
DOI 10.1038/nbt1344, PII NBT1344
-
Rother RP, Rollins SA, Mojcik CF, Brodsky RA, Bell L. Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria. Nat Biotechnol. 2007;25:1256-1264. (Pubitemid 350076509)
-
(2007)
Nature Biotechnology
, vol.25
, Issue.11
, pp. 1256-1264
-
-
Rother, R.P.1
Rollins, S.A.2
Mojcik, C.F.3
Brodsky, R.A.4
Bell, L.5
-
37
-
-
70449503797
-
Paroxysmal nocturnal hemoglobinuria
-
Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Philadelphia, PA: Churchill Livingstone
-
Brodsky RA. Paroxysmal nocturnal hemoglobinuria. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. Philadelphia, PA: Churchill Livingstone; 2009: 385-394.
-
(2009)
Hematology: Basic Principles and Practice
, pp. 385-394
-
-
Brodsky, R.A.1
-
38
-
-
33748904355
-
The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria
-
DOI 10.1056/NEJMoa061648
-
Hillmen P, Young NS, Schubert J, et al. The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria. N Engl J Med. 2006; 355:1233-1243. (Pubitemid 44427447)
-
(2006)
New England Journal of Medicine
, vol.355
, Issue.12
, pp. 1233-1243
-
-
Hillmen, P.1
Young, N.S.2
Schubert, J.3
Brodsky, R.A.4
Socie, G.5
Muus, P.6
Roth, A.7
Szer, J.8
Elebute, M.O.9
Nakamura, R.10
Browne, P.11
Risitano, A.M.12
Hill, A.13
Schrezenmeier, H.14
Fu, C.-L.15
Maciejewski, J.16
Rollins, S.A.17
Mojcik, C.F.18
Rother, R.P.19
Luzzatto, L.20
more..
-
39
-
-
41349089713
-
Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria
-
Brodsky RA, Young NS, Antonioli E, et al. Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria. Blood. 2008; 111:1840-1847.
-
(2008)
Blood
, vol.111
, pp. 1840-1847
-
-
Brodsky, R.A.1
Young, N.S.2
Antonioli, E.3
-
40
-
-
35948962168
-
Effect of the complement inhibitor eculizumab on thromboembolism in patients with paroxysmal nocturnal hemoglobinuria
-
DOI 10.1182/blood-2007-06-095646
-
Hillmen P, Muus P, Duhrsen U, et al. Effect of the complement inhibitor eculizumab on thromboembolism in patients with paroxysmal nocturnal hemoglobinuria. Blood. 2007;110:4123-4128. (Pubitemid 350248472)
-
(2007)
Blood
, vol.110
, Issue.12
, pp. 4123-4128
-
-
Hillmen, P.1
Muus, P.2
Duhrsen, U.3
Risitano, A.M.4
Schubert, J.5
Luzzatto, L.6
Schrezenmeier, H.7
Szer, J.8
Brodsky, R.A.9
Hill, A.10
Socie, G.11
Bessler, M.12
Rollins, S.A.13
Bell, L.14
Rother, R.P.15
Young, N.S.16
-
41
-
-
18744411547
-
Aplastic anaemia
-
Brodsky RA, Jones RJ. Aplastic anaemia. Lancet. 2005;365:1647-1656.
-
(2005)
Lancet
, vol.365
, pp. 1647-1656
-
-
Brodsky, R.A.1
Jones, R.J.2
-
42
-
-
0037006957
-
Acquired aplastic anemia
-
Young NS. Acquired aplastic anemia. Ann Intern Med. 2002;136:534-546.
-
(2002)
Ann Intern Med
, vol.136
, pp. 534-546
-
-
Young, N.S.1
-
43
-
-
65449188713
-
Complement fraction 3 binding on erythrocytes as additional mechanism of disease in paroxysmal nocturnal hemoglobinuria patients treated by eculizumab
-
Risitano AM, Notaro R, Marando L, et al. Complement fraction 3 binding on erythrocytes as additional mechanism of disease in paroxysmal nocturnal hemoglobinuria patients treated by eculizumab. Blood. 2009;113:4094-4100.
-
(2009)
Blood
, vol.113
, pp. 4094-4100
-
-
Risitano, A.M.1
Notaro, R.2
Marando, L.3
-
44
-
-
47249151012
-
Eculizumab, a terminal complement inhibitor, improves anaemia in patients with paroxysmal nocturnal haemoglobinuria
-
May 22 [Epub ahead of print]
-
Schubert J, Hillmen P, Roth A, et al. Eculizumab, a terminal complement inhibitor, improves anaemia in patients with paroxysmal nocturnal haemoglobinuria. Br J Haematol. 2008 May 22 [Epub ahead of print].
-
(2008)
Br J Haematol
-
-
Schubert, J.1
Hillmen, P.2
Roth, A.3
-
45
-
-
0032936695
-
Bone marrow transplants for paroxysmal nocturnal haemoglobinuria
-
Saso R, Marsh J, Cevreska L, et al. Bone marrow transplants for paroxysmal nocturnal haemoglobinuria. Br J Haematol. 1999;104:392-396.
-
(1999)
Br J Haematol
, vol.104
, pp. 392-396
-
-
Saso, R.1
Marsh, J.2
Cevreska, L.3
-
46
-
-
70349760901
-
Stem cell transplantation for paroxysmal nocturnal hemoglobinuria: An ongoing joint study of the AAWP EBMT group and the French Society of Hematology
-
abstract. Abstract 1181
-
Perfault de Latour R, Schrezenmeier H, Mary JY, et al. Stem cell transplantation for paroxysmal nocturnal hemoglobinuria: an ongoing joint study of the AAWP EBMT group and the French Society of Hematology [abstract]. Blood. 2008;112:Abstract 1181.
-
(2008)
Blood
, vol.112
-
-
De Perfault Latour, R.1
Schrezenmeier, H.2
Mary, J.Y.3
-
47
-
-
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, et al. 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
-
48
-
-
0035194794
-
Conditioning with high-dose cyclophosphamide may not be sufficient to provide a long-term remission of paroxysmal nocturnal hemoglobinuria following syngeneic peripheral blood stem cell transplantation
-
Cho SG, Lim J, Kim Y, et al. Conditioning with high-dose cyclophosphamide may not be sufficient to provide a long-term remission of paroxysmal nocturnal hemoglobinuria following syngeneic peripheral blood stem cell transplantation. Bone Marrow Transplant. 2001;28:987-988.
-
(2001)
Bone Marrow Transplant
, vol.28
, pp. 987-988
-
-
Cho, S.G.1
Lim, J.2
Kim, Y.3
-
49
-
-
0035019054
-
Successful application of nonmyeloablative transplantation for paroxysmal nocturnal hemoglobinuria
-
DOI 10.1016/S0301-472X(01)00632-4, PII S0301472X01006324
-
Suenaga K, Kanda Y, Niiya H, et al. Successful application of nonmyeloablative transplantation for paroxysmal nocturnal hemoglobinuria. Exp Hematol. 2001;29:639-642. (Pubitemid 32463902)
-
(2001)
Experimental Hematology
, vol.29
, Issue.5
, pp. 639-642
-
-
Suenaga, K.1
Kanda, Y.2
Niiya, H.3
Nakai, K.4
Saito, T.5
Saito, A.6
Ohnishi, M.7
Takeuchi, T.8
Tanosaki, R.9
Makimoto, A.10
Miyawaki, S.11
Ohnishi, T.12
Kanai, S.13
Tobinai, K.14
Takaue, Y.15
Mineishi, S.16
-
50
-
-
55549090680
-
Reduced intensity HLA-haploidentical BMT with post transplantation cyclophosphamide in nonmalignant hematologic diseases
-
Brodsky RA, Luznik L, Bolanos-Meade J, et al. Reduced intensity HLA-haploidentical BMT with post transplantation cyclophosphamide in nonmalignant hematologic diseases. Bone Marrow Transplant. 2008;42:523-527.
-
(2008)
Bone Marrow Transplant
, vol.42
, pp. 523-527
-
-
Brodsky, R.A.1
Luznik, L.2
Bolanos-Meade, J.3
-
51
-
-
33746881457
-
Catheter-directed thrombolysis and thrombectomy for the Budd- Chiari syndrome in paroxysmal nocturnal hemoglobinuria in three patients
-
Kuo GP, Brodsky RA, Kim HS. Catheter-directed thrombolysis and thrombectomy for the Budd- Chiari syndrome in paroxysmal nocturnal hemoglobinuria in three patients. J Vasc Interv Radiol. 2006;17:383-387.
-
(2006)
J Vasc Interv Radiol
, vol.17
, pp. 383-387
-
-
Kuo, G.P.1
Brodsky, R.A.2
Kim, H.S.3
-
52
-
-
0242494954
-
Primary prophylaxis with warfarin prevents thrombosis in paroxysmal nocturnal hemoglobinuria (PNH)
-
DOI 10.1182/blood-2003-01-0009
-
Hall C, Richards S, Hillmen P. Primary prophylaxis with warfarin prevents thrombosis in paroxysmal nocturnal hemoglobinuria (PNH). Blood. 2003;102:3587-3591. (Pubitemid 37409375)
-
(2003)
Blood
, vol.102
, Issue.10
, pp. 3587-3591
-
-
Hall, C.1
Richards, S.2
Hillmen, P.3
-
53
-
-
0033808293
-
Paroxysmal nocturnal hemoglobinuria and the risk of venous thrombosis: Review and recommendations for management of the pregnant and nonpregnant patient
-
Ray JG, Burows RF, Ginsberg JS, Burrows EA. Paroxysmal nocturnal hemoglobinuria and the risk of venous thrombosis: review and recommendations for management of the pregnant and nonpregnant patient. Haemostasis. 2000;30:103-117.
-
(2000)
Haemostasis
, vol.30
, pp. 103-117
-
-
Ray, J.G.1
Burows, R.F.2
Ginsberg, J.S.3
Burrows, E.A.4
-
54
-
-
63349111169
-
Paroxysmal nocturnal hemoglobinuria (PNH) and pregnancy in the era of eculizumab
-
Danilov AV, Smith H, Craigo S, et al. Paroxysmal nocturnal hemoglobinuria (PNH) and pregnancy in the era of eculizumab. Leuk Res. 2009;33:e4-e5.
-
(2009)
Leuk Res
, vol.33
-
-
Danilov, A.V.1
Smith, H.2
Craigo, S.3
|