-
1
-
-
33947227491
-
The pathophysiology of paroxysmal nocturnal hemoglobinuria
-
Parker C.J. The pathophysiology of paroxysmal nocturnal hemoglobinuria. Exp Hematol 35 (2007) 523-533
-
(2007)
Exp Hematol
, vol.35
, pp. 523-533
-
-
Parker, C.J.1
-
2
-
-
0028802581
-
Defective glycosyl phosphatidylinositol anchor synthesis and paroxysmal nocturnal hemoglobinuria
-
Kinoshita T., Inoue N., and Takeda J. Defective glycosyl phosphatidylinositol anchor synthesis and paroxysmal nocturnal hemoglobinuria. Adv Immunol 60 (1995) 57-103
-
(1995)
Adv Immunol
, vol.60
, pp. 57-103
-
-
Kinoshita, T.1
Inoue, N.2
Takeda, J.3
-
3
-
-
28444483571
-
Diagnosis and management of paroxysmal nocturnal hemoglobinuria
-
Parker C., Omine M., Richards S., et al. Diagnosis and management of paroxysmal nocturnal hemoglobinuria. Blood 106 (2005) 3699-3709
-
(2005)
Blood
, vol.106
, pp. 3699-3709
-
-
Parker, C.1
Omine, M.2
Richards, S.3
-
4
-
-
0033230376
-
Different roles of glycosylphosphatidylinositol in various hematopoietic cells as revealed by a mouse model of paroxysmal nocturnal hemoglobinuria
-
Murakami Y., Kinoshita T., Maeda Y., Nakano T., Kosaka H., and Takeda J. Different roles of glycosylphosphatidylinositol in various hematopoietic cells as revealed by a mouse model of paroxysmal nocturnal hemoglobinuria. Blood 94 (1999) 2963-2970
-
(1999)
Blood
, vol.94
, pp. 2963-2970
-
-
Murakami, Y.1
Kinoshita, T.2
Maeda, Y.3
Nakano, T.4
Kosaka, H.5
Takeda, J.6
-
5
-
-
33845494914
-
Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH)
-
Inoue N., Izui-Sarumaru T., Murakami Y., et al. Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH). Blood 108 (2006) 4232-4236
-
(2006)
Blood
, vol.108
, pp. 4232-4236
-
-
Inoue, N.1
Izui-Sarumaru, T.2
Murakami, Y.3
-
6
-
-
33748904355
-
The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria
-
Hillmen P., Young N.S., Schubert J., et al. The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria. N Engl J Med 355 (2006) 1233-1243
-
(2006)
N Engl J Med
, vol.355
, pp. 1233-1243
-
-
Hillmen, P.1
Young, N.S.2
Schubert, J.3
-
7
-
-
35948962168
-
Effect of the complement inhibitor eculizumab on thromboembolism in patients with paroxysmal nocturnal hemoglobinuria
-
Hillmen P., Muus P., Dührsen U., et al. Effect of the complement inhibitor eculizumab on thromboembolism in patients with paroxysmal nocturnal hemoglobinuria. Blood 110 (2007) 4123-4128
-
(2007)
Blood
, vol.110
, pp. 4123-4128
-
-
Hillmen, P.1
Muus, P.2
Dührsen, U.3
-
8
-
-
32644434385
-
Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia
-
Sugimori C., Chuhjo T., Feng X., et al. Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia. Blood 107 (2006) 1308-1314
-
(2006)
Blood
, vol.107
, pp. 1308-1314
-
-
Sugimori, C.1
Chuhjo, T.2
Feng, X.3
-
9
-
-
0041737643
-
Polyclonal hematopoiesis maintained in patients with bone marrow failure harboring a minor population of paroxysmal nocturnal hemoglobinuria-type cells
-
Ishiyama K., Chuhjo T., Wang H., Yachie A., Omine M., and Nakao S. Polyclonal hematopoiesis maintained in patients with bone marrow failure harboring a minor population of paroxysmal nocturnal hemoglobinuria-type cells. Blood 102 (2003) 1211-1216
-
(2003)
Blood
, vol.102
, pp. 1211-1216
-
-
Ishiyama, K.1
Chuhjo, T.2
Wang, H.3
Yachie, A.4
Omine, M.5
Nakao, S.6
-
10
-
-
0029899213
-
Syngeneic bone marrow transplantation without conditioning in a patient with paroxysmal nocturnal hemoglobinuria: in vivo evidence that the mutant stem cells have a survival advantage
-
Endo M., Beatty P.G., Vreeke T.M., Wittwer C.T., Singh S.P., and Parker C.J. Syngeneic bone marrow transplantation without conditioning in a patient with paroxysmal nocturnal hemoglobinuria: in vivo evidence that the mutant stem cells have a survival advantage. Blood 88 (1996) 742-750
-
(1996)
Blood
, vol.88
, pp. 742-750
-
-
Endo, M.1
Beatty, P.G.2
Vreeke, T.M.3
Wittwer, C.T.4
Singh, S.P.5
Parker, C.J.6
-
11
-
-
0032897237
-
Bone marrow transplantation for paroxysmal nocturnal haemoglobinuria
-
Bemba M., Guardiola P., Garderet L., et al. Bone marrow transplantation for paroxysmal nocturnal haemoglobinuria. Br J Haematol 105 (1999) 366-368
-
(1999)
Br J Haematol
, vol.105
, pp. 366-368
-
-
Bemba, M.1
Guardiola, P.2
Garderet, L.3
-
12
-
-
0033951380
-
Bone marrow transplantation for paroxysmal nocturnal hemoglobinuria
-
Raiola A.M., Van Lint M.T., Lamparelli T., et al. Bone marrow transplantation for paroxysmal nocturnal hemoglobinuria. Haematologica 85 (2000) 59-62
-
(2000)
Haematologica
, vol.85
, pp. 59-62
-
-
Raiola, A.M.1
Van Lint, M.T.2
Lamparelli, T.3
-
13
-
-
9144244793
-
Hematopoietic cell transplantation from related and unrelated donors after minimal conditioning as a curative treatment modality for severe paroxysmal nocturnal hemoglobinuria
-
Hegenbart U., Niederwieser D., Forman S., et al. Hematopoietic cell transplantation from related and unrelated donors after minimal conditioning as a curative treatment modality for severe paroxysmal nocturnal hemoglobinuria. Biol Blood Marrow Transplant 9 (2003) 689-697
-
(2003)
Biol Blood Marrow Transplant
, vol.9
, pp. 689-697
-
-
Hegenbart, U.1
Niederwieser, D.2
Forman, S.3
-
14
-
-
0842285673
-
In vitro and in vivo evidence of PNH cell sensitivity to immune attack after nonmyeloablative allogeneic hematopoietic cell transplantation
-
Takahashi Y., McCoy J.P., Carvallo C., et al. In vitro and in vivo evidence of PNH cell sensitivity to immune attack after nonmyeloablative allogeneic hematopoietic cell transplantation. Blood 103 (2004) 1383-1390
-
(2004)
Blood
, vol.103
, pp. 1383-1390
-
-
Takahashi, Y.1
McCoy, J.P.2
Carvallo, C.3
-
15
-
-
0035038581
-
Successful unrelated donor bone marrow transplantation for paroxysmal nocturnal hemoglobinuria
-
Woodard P., Wang W., Pitts N., et al. Successful unrelated donor bone marrow transplantation for paroxysmal nocturnal hemoglobinuria. Bone Marrow Transplant 27 (2001) 589-592
-
(2001)
Bone Marrow Transplant
, vol.27
, pp. 589-592
-
-
Woodard, P.1
Wang, W.2
Pitts, N.3
-
16
-
-
0025999919
-
Paroxysmal nocturnal hemoglobinuria with onset in childhood and adolescence
-
Ware R.E., Hall S.E., and Rosse W.F. Paroxysmal nocturnal hemoglobinuria with onset in childhood and adolescence. N Engl J Med 325 (1991) 991-996
-
(1991)
N Engl J Med
, vol.325
, pp. 991-996
-
-
Ware, R.E.1
Hall, S.E.2
Rosse, W.F.3
-
17
-
-
14144255205
-
Childhood paroxysmal nocturnal haemoglobinuria (PNH), a report of 11 cases in The Netherlands
-
van den Heuvel-Eibrink M.M., Bredius R.G.M., te Winkel M.L., et al. Childhood paroxysmal nocturnal haemoglobinuria (PNH), a report of 11 cases in The Netherlands. Br J Haematol 128 (2005) 571-577
-
(2005)
Br J Haematol
, vol.128
, pp. 571-577
-
-
van den Heuvel-Eibrink, M.M.1
Bredius, R.G.M.2
te Winkel, M.L.3
-
18
-
-
18744411547
-
Aplastic anaemia
-
Brodsky R.A., and Jones R.J. Aplastic anaemia. Lancet 365 (2005) 1647-1656
-
(2005)
Lancet
, vol.365
, pp. 1647-1656
-
-
Brodsky, R.A.1
Jones, R.J.2
-
19
-
-
43049090537
-
Narrative review: paroxysmal nocturnal hemoglobinuria: the physiology of complement-related hemolytic anemia
-
Brodsky R.A. Narrative review: paroxysmal nocturnal hemoglobinuria: the physiology of complement-related hemolytic anemia. Ann Intern. Med 148 (2008) 587-595
-
(2008)
Ann Intern. Med
, vol.148
, pp. 587-595
-
-
Brodsky, R.A.1
-
20
-
-
0034502010
-
Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin
-
Brodsky R.A., Mukhina G.L., Li S., et al. Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin. Am J Clin Pathol 114 (2000) 459-466
-
(2000)
Am J Clin Pathol
, vol.114
, pp. 459-466
-
-
Brodsky, R.A.1
Mukhina, G.L.2
Li, S.3
-
21
-
-
33644505823
-
Quantitative analysis of bone marrow CD34 cells in aplastic anemia and hypoplastic myelodysplastic syndromes
-
Matsui W.H., Brodsky R.A., Smith B.D., Borowitz M.J., and Jones R.J. Quantitative analysis of bone marrow CD34 cells in aplastic anemia and hypoplastic myelodysplastic syndromes. Leukemia 20 (2006) 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
-
22
-
-
0035724869
-
Multilineage glycosylphosphatidylinositol anchor-deficient haematopoiesis in untreated aplastic anaemia
-
Mukhina G.L., Buckley J.T., Barber J.P., Jones R.J., and Brodsky R.A. Multilineage glycosylphosphatidylinositol anchor-deficient haematopoiesis in untreated aplastic anaemia. Br J Haematol 115 (2001) 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
-
23
-
-
0036893544
-
Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome
-
Wang H., Chuhjo T., Yasue S., Omine M., and Nakao S. Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome. Blood 100 (2002) 3897-3902
-
(2002)
Blood
, vol.100
, pp. 3897-3902
-
-
Wang, H.1
Chuhjo, T.2
Yasue, S.3
Omine, M.4
Nakao, S.5
-
24
-
-
0037420270
-
Antithymocyte globulin and cyclosporine for severe aplastic anemia: association between hematologic response and long-term outcome
-
Rosenfeld S., Follmann D., Nunez O., and Young N.S. Antithymocyte globulin and cyclosporine for severe aplastic anemia: association between hematologic response and long-term outcome. JAMA 289 (2003) 1130-1135
-
(2003)
JAMA
, vol.289
, pp. 1130-1135
-
-
Rosenfeld, S.1
Follmann, D.2
Nunez, O.3
Young, N.S.4
-
25
-
-
0035797919
-
Durable treatment-free remission after high-dose cyclophosphamide therapy for previously untreated severe aplastic anemia
-
Brodsky R.A., Sensenbrenner L.L., Smith B.D., et al. Durable treatment-free remission after high-dose cyclophosphamide therapy for previously untreated severe aplastic anemia. Ann Intern. Med 135 (2001) 477-483
-
(2001)
Ann Intern. Med
, vol.135
, pp. 477-483
-
-
Brodsky, R.A.1
Sensenbrenner, L.L.2
Smith, B.D.3
-
26
-
-
33748157848
-
Optimization of conditioning for marrow transplantation from unrelated donors for patients with aplastic anemia after failure of immunosuppressive therapy
-
Deeg H.J., O'Donnell M., Tolar J., et al. Optimization of conditioning for marrow transplantation from unrelated donors for patients with aplastic anemia after failure of immunosuppressive therapy. Blood 108 (2006) 1485-1491
-
(2006)
Blood
, vol.108
, pp. 1485-1491
-
-
Deeg, H.J.1
O'Donnell, M.2
Tolar, J.3
-
28
-
-
35148829886
-
A molecular classification of congenital neutropenia syndromes
-
Boxer L.A., and Newburger P.E. A molecular classification of congenital neutropenia syndromes. Pediatr Blood Cancer 49 (2007) 609-614
-
(2007)
Pediatr Blood Cancer
, vol.49
, pp. 609-614
-
-
Boxer, L.A.1
Newburger, P.E.2
-
29
-
-
33845274520
-
Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia
-
Carlsson G., Andersson M., Pütsep K., et al. Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia. Acta Pædiatr 95 (2006) 1526-1532
-
(2006)
Acta Pædiatr
, vol.95
, pp. 1526-1532
-
-
Carlsson, G.1
Andersson, M.2
Pütsep, K.3
-
30
-
-
33749478463
-
The Severe Chronic Neutropenia International Registry: 10-year follow-up report
-
Dale D.C., Bolyard A.A., Schwinzer B.G., et al. The Severe Chronic Neutropenia International Registry: 10-year follow-up report. Support Cancer Ther 3 (2006) 220-231
-
(2006)
Support Cancer Ther
, vol.3
, pp. 220-231
-
-
Dale, D.C.1
Bolyard, A.A.2
Schwinzer, B.G.3
-
31
-
-
47049090395
-
Lessons from congenital neutropenia: 50 years of progress in understanding myelopoiesis
-
Berliner N. Lessons from congenital neutropenia: 50 years of progress in understanding myelopoiesis. Blood 111 (2008) 5427-5432
-
(2008)
Blood
, vol.111
, pp. 5427-5432
-
-
Berliner, N.1
-
32
-
-
0035525791
-
Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease
-
Ancliff P.J., Gale R.E., Liesner R., Hann I.M., and Linch D.C. Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease. Blood 98 (2001) 2645-2650
-
(2001)
Blood
, vol.98
, pp. 2645-2650
-
-
Ancliff, P.J.1
Gale, R.E.2
Liesner, R.3
Hann, I.M.4
Linch, D.C.5
-
33
-
-
33845904894
-
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
-
Klein C., Grudzien M., Appaswamy G., et al. HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nat Genet 39 (2007) 86-92
-
(2007)
Nat Genet
, vol.39
, pp. 86-92
-
-
Klein, C.1
Grudzien, M.2
Appaswamy, G.3
-
34
-
-
0027269718
-
A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (filgrastim) for treatment of severe chronic neutropenia
-
Dale D.C., Bonilla M.A., Davis M.W., et al. A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (filgrastim) for treatment of severe chronic neutropenia. Blood 81 (1993) 2496-2502
-
(1993)
Blood
, vol.81
, pp. 2496-2502
-
-
Dale, D.C.1
Bonilla, M.A.2
Davis, M.W.3
-
35
-
-
33745096897
-
The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy
-
Rosenberg P.S., Alter B.P., Bolyard A.A., et al. The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy. Blood 107 (2006) 4628-4635
-
(2006)
Blood
, vol.107
, pp. 4628-4635
-
-
Rosenberg, P.S.1
Alter, B.P.2
Bolyard, A.A.3
-
36
-
-
47149086005
-
G-CSF receptor mutations in patients with congenital neutropenia
-
Germeshausen M., Skokowa J., Ballmaier M., Zeidler C., and Welte K. G-CSF receptor mutations in patients with congenital neutropenia. Curr Opin Hematol 15 (2008) 332-337
-
(2008)
Curr Opin Hematol
, vol.15
, pp. 332-337
-
-
Germeshausen, M.1
Skokowa, J.2
Ballmaier, M.3
Zeidler, C.4
Welte, K.5
-
37
-
-
0034651925
-
Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation
-
Zeidler C., Welte K., Barak Y., et al. Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation. Blood 95 (2000) 1195-1198
-
(2000)
Blood
, vol.95
, pp. 1195-1198
-
-
Zeidler, C.1
Welte, K.2
Barak, Y.3
-
38
-
-
2442656658
-
Umbilical cord blood stem cell transplantation from unrelated HLA-matched donor in an infant with severe congenital neutropenia
-
Mino E., Kobayashi R., Yoshida M., Suzuki Y., Yamada M., and Kobayashi K. Umbilical cord blood stem cell transplantation from unrelated HLA-matched donor in an infant with severe congenital neutropenia. Bone Marrow Transplant 33 (2004) 969-971
-
(2004)
Bone Marrow Transplant
, vol.33
, pp. 969-971
-
-
Mino, E.1
Kobayashi, R.2
Yoshida, M.3
Suzuki, Y.4
Yamada, M.5
Kobayashi, K.6
-
39
-
-
33750166385
-
Unrelated bone marrow transplantation using a reduced-intensity conditioning regimen for the treatment of Kostmann syndrome
-
Fukano R., Nagatoshi Y., Shinkoda Y., et al. Unrelated bone marrow transplantation using a reduced-intensity conditioning regimen for the treatment of Kostmann syndrome. Bone Marrow Transplant 38 (2006) 635-636
-
(2006)
Bone Marrow Transplant
, vol.38
, pp. 635-636
-
-
Fukano, R.1
Nagatoshi, Y.2
Shinkoda, Y.3
-
40
-
-
19944427804
-
Hematopoietic stem cell transplantation in severe congenital neutropenia: experience of the French SCN register
-
Ferry C., Ouachée M., Leblanc T., et al. Hematopoietic stem cell transplantation in severe congenital neutropenia: experience of the French SCN register. Bone Marrow Transplant 35 (2005) 45-50
-
(2005)
Bone Marrow Transplant
, vol.35
, pp. 45-50
-
-
Ferry, C.1
Ouachée, M.2
Leblanc, T.3
-
41
-
-
15544363068
-
Stem cell transplantation in patients with severe congenital neutropenia with evidence of leukemic transformation
-
Choi S.W., Boxer L.A., Pulsipher M.A., et al. Stem cell transplantation in patients with severe congenital neutropenia with evidence of leukemic transformation. Bone Marrow Transplant 35 (2005) 473-477
-
(2005)
Bone Marrow Transplant
, vol.35
, pp. 473-477
-
-
Choi, S.W.1
Boxer, L.A.2
Pulsipher, M.A.3
|