-
3
-
-
31044431526
-
Characterization of inhibitors in congenital hemophilia
-
Rodriguez-Merchan EC, Lee CA, eds. Oxford, UK: Blackwell
-
Peerlinck K, Jacquemin M. Characterization of inhibitors in congenital hemophilia. In: Rodriguez-Merchan EC, Lee CA, eds. Inhibitors in Patients with Haemophilia. Oxford, UK: Blackwell; 2002:9-13.
-
(2002)
Inhibitors in Patients with Haemophilia
, pp. 9-13
-
-
Peerlinck, K.1
Jacquemin, M.2
-
4
-
-
0033695026
-
Factor VIII inhibitor with catalytic activity towards factor VIII
-
Lacroix-Desmazes S, Sooryanarayana, Moreau A, Kazatchkine MD, Kaveri SV. Factor VIII inhibitor with catalytic activity towards factor VIII. Haematologica. 2000;85(suppl):89-92.
-
(2000)
Haematologica
, vol.85
, Issue.SUPPL.
, pp. 89-92
-
-
Lacroix-Desmazes, S.1
Sooryanarayana2
Moreau, A.3
Kazatchkine, M.D.4
Kaveri, S.V.5
-
5
-
-
0024328077
-
Molecular basis of factor VIII inhibition by human antibodies: Antibodies that bind to the factor VIII light chain prevent the interaction of factor VIII with phospholipid
-
Arai M, Scandella D, Hover LW. Molecular basis of factor VIII inhibition by human antibodies: antibodies that bind to the factor VIII light chain prevent the interaction of factor VIII with phospholipid. J Clin Invest. 1989;83:1978-1984.
-
(1989)
J Clin Invest
, vol.83
, pp. 1978-1984
-
-
Arai, M.1
Scandella, D.2
Hover, L.W.3
-
6
-
-
0027457180
-
A factor VIII neutralizing monoclonal antibody and a human inhibitor alloantibody recognizing epitopes in the C2 domain inhibit factor VIII binding to von Willebrand factor and to phosphatidylserine
-
Shima M, Scandella D, Yoshioka A, et al. A factor VIII neutralizing monoclonal antibody and a human inhibitor alloantibody recognizing epitopes in the C2 domain inhibit factor VIII binding to von Willebrand factor and to phosphatidylserine. Thromb Haemost. 1993;69:240-246.
-
(1993)
Thromb Haemost
, vol.69
, pp. 240-246
-
-
Shima, M.1
Scandella, D.2
Yoshioka, A.3
-
7
-
-
0018876848
-
Circulating immune complexes containing anti-FVIII antibodies in multitransfused patients with hemophilia A
-
Kazatchkine MD, Sultan Y, Burton-Kee EJ, Mowbray JF. Circulating immune complexes containing anti-FVIII antibodies in multitransfused patients with hemophilia A. Clin Exp Immunol. 1980;39:315-320.
-
(1980)
Clin Exp Immunol
, vol.39
, pp. 315-320
-
-
Kazatchkine, M.D.1
Sultan, Y.2
Burton-Kee, E.J.3
Mowbray, J.F.4
-
8
-
-
0026548917
-
Incidence of development of factor VIII and factor IX inhibitors in haemophiliacs
-
Ehrenforth S, Kreuz W, Scharrer I, et al. Incidence of development of factor VIII and factor IX inhibitors in haemophiliacs. Lancet. 1992;339:594-598.
-
(1992)
Lancet
, vol.339
, pp. 594-598
-
-
Ehrenforth, S.1
Kreuz, W.2
Scharrer, I.3
-
9
-
-
0001757605
-
Transient inhibitors in patients with hemophilia A
-
Abstract 1804
-
Brown DL, Bray GL, Scharrer I. Transient inhibitors in patients with hemophilia A [abstract]. Thromb Haemost. 1999;82(suppl):573. Abstract 1804.
-
(1999)
Thromb Haemost
, vol.82
, Issue.SUPPL.
, pp. 573
-
-
Brown, D.L.1
Bray, G.L.2
Scharrer, I.3
-
10
-
-
0028266130
-
A multicenter study of recombinant factor VIII (Recombinate): Safety, efficacy and inhibitor risk in previously untreated individuals with hemophilia A
-
The Recombinate Study Group
-
Bray GL, Gomperts ED, Courter S, et al. A multicenter study of recombinant factor VIII (Recombinate): safety, efficacy and inhibitor risk in previously untreated individuals with hemophilia A. The Recombinate Study Group. Blood. 1994;83:2428-2435.
-
(1994)
Blood
, vol.83
, pp. 2428-2435
-
-
Bray, G.L.1
Gomperts, E.D.2
Courter, S.3
-
11
-
-
0003287371
-
A four-year update of safety and efficacy of an albumin-free formulated B-domain deleted factor VIII (BBD rFVIII, rVIIISQ) in previously untreated severe hemophilia A patients
-
Lusher JM, Spira J, Rodriguez D. A four-year update of safety and efficacy of an albumin-free formulated B-domain deleted factor VIII (BBD rFVIII, rVIIISQ) in previously untreated severe hemophilia A patients. Thromb Haemost. 1999;82:1493.
-
(1999)
Thromb Haemost
, vol.82
, pp. 1493
-
-
Lusher, J.M.1
Spira, J.2
Rodriguez, D.3
-
12
-
-
0347662157
-
Surveillance for factor VIII inhibitor development in the Canadian hemophilia A population following the widespread introduction of recombinant factor VIII replacement therapy
-
Giles AR, Rivard GE, Teitel J, Walker I. Surveillance for factor VIII inhibitor development in the Canadian hemophilia A population following the widespread introduction of recombinant factor VIII replacement therapy. Transfus Sci. 1998;19:139-148.
-
(1998)
Transfus Sci
, vol.19
, pp. 139-148
-
-
Giles, A.R.1
Rivard, G.E.2
Teitel, J.3
Walker, I.4
-
13
-
-
3042585962
-
Epidemiology of inhibitors and current treatment strategies
-
Kreuz W, Ettingshausen CE, Auerswald G, et al, for the GTH PUP Study Group. Epidemiology of inhibitors and current treatment strategies. Haematologica. 2003;88:EREP04.
-
(2003)
Haematologica
, vol.88
-
-
Kreuz, W.1
Ettingshausen, C.E.2
Auerswald, G.3
-
14
-
-
0016853978
-
Proceedings: A more uniform measurement of factor VIII inhibitors
-
Kasper CK, Aledort L, Aronson D, et al. Proceedings: a more uniform measurement of factor VIII inhibitors [letter]. Thromb Diath Haemorrh. 1975;34:612.
-
(1975)
Thromb Diath Haemorrh
, vol.34
, pp. 612
-
-
Kasper, C.K.1
Aledort, L.2
Aronson, D.3
-
15
-
-
0028837315
-
The Nijmegen modification of the Bethesda assay for factor VIII:C inhibitors: Improved specificity and reliability
-
Verbruggen B, Novakova I, Wessels H, et al. The Nijmegen modification of the Bethesda assay for factor VIII:C inhibitors: improved specificity and reliability. Thromb Haemost. 1995;73:247-251.
-
(1995)
Thromb Haemost
, vol.73
, pp. 247-251
-
-
Verbruggen, B.1
Novakova, I.2
Wessels, H.3
-
16
-
-
0037810801
-
The management of inhibitors in hemophilia A: Introduction and systematic review of current practice
-
Paisley S, Wight J, Currie E, Knight C. The management of inhibitors in hemophilia A: introduction and systematic review of current practice. Haemophilia. 2003;9:405-417.
-
(2003)
Haemophilia
, vol.9
, pp. 405-417
-
-
Paisley, S.1
Wight, J.2
Currie, E.3
Knight, C.4
-
17
-
-
0035077234
-
Definitions in hemophilia: Recommendation of the scientific subcommittee on factor VIII and factor IX of the Scientific and Standardization Committee of the International Society on Thrombosis and Hemostasis
-
White GC 2nd, Rosendaal F, Aledort L, Lusher JM, Rothschild C, Ingerslev J, for the Factor VIII and Factor IX Subcommittee. Definitions in hemophilia: recommendation of the scientific subcommittee on factor VIII and factor IX of the Scientific and Standardization Committee of the International Society on Thrombosis and Hemostasis. Thromb Haemost. 2001;85:560.
-
(2001)
Thromb Haemost
, vol.85
, pp. 560
-
-
White II, G.C.1
Rosendaal, F.2
Aledort, L.3
Lusher, J.M.4
Rothschild, C.5
Ingerslev, J.6
-
18
-
-
13644275038
-
Immunochemistry of factor VIII:C inhibitor antibodies
-
Fulcher CA. Immunochemistry of factor VIII:C inhibitor antibodies. Am J Med. 1991;91:6S-8S.
-
(1991)
Am J Med
, vol.91
-
-
Fulcher, C.A.1
-
19
-
-
0027488655
-
Anti-factor VIII antibodies of hemophiliac patients are frequently directed towards nonfunctional determinants and do not exhibit isotypic restriction
-
Gilles JG, Arnout J, Vermylen J, Saint-Remy JM. Anti-factor VIII antibodies of hemophiliac patients are frequently directed towards nonfunctional determinants and do not exhibit isotypic restriction. Blood. 1993;82:2452-2461.
-
(1993)
Blood
, vol.82
, pp. 2452-2461
-
-
Gilles, J.G.1
Arnout, J.2
Vermylen, J.3
Saint-Remy, J.M.4
-
20
-
-
0036207024
-
Haemophilia A: Effects of inhibitory antibodies on factor VIII functional interactions and approaches to prevent their action
-
Saenko EL, Ananyeva NM, Kouiavskaia DV, et al. Haemophilia A: effects of inhibitory antibodies on factor VIII functional interactions and approaches to prevent their action. Haemophilia. 2002;8:1-11.
-
(2002)
Haemophilia
, vol.8
, pp. 1-11
-
-
Saenko, E.L.1
Ananyeva, N.M.2
Kouiavskaia, D.V.3
-
21
-
-
1842380604
-
Localization of human factor VIII epitopes to two polypeptide fragments
-
Fulcher CA, De Graaf Mahoney S, Roberts JR, Kasper CK, Zimmerman TS. Localization of human factor VIII epitopes to two polypeptide fragments. Proc Natl Acad Sci U S A. 1985;82:7728-7732.
-
(1985)
Proc Natl Acad Sci U S A
, vol.82
, pp. 7728-7732
-
-
Fulcher, C.A.1
De Graaf Mahoney, S.2
Roberts, J.R.3
Kasper, C.K.4
Zimmerman, T.S.5
-
23
-
-
0036282373
-
Inhibitor development in previously untreated patients with hemophilia A: A prospective long-term follow-up comparing plasma-derived and recombinant products
-
Kreuz W, Ettingshausen CE, Zyschka A, et al. Inhibitor development in previously untreated patients with hemophilia A: a prospective long-term follow-up comparing plasma-derived and recombinant products. Semin Thromb Hemost. 2002;28:285-290.
-
(2002)
Semin Thromb Hemost
, vol.28
, pp. 285-290
-
-
Kreuz, W.1
Ettingshausen, C.E.2
Zyschka, A.3
-
24
-
-
11044225185
-
Genetic basis of inhibitor development in severe hemophilia A and B
-
Rodriguez-Merchan EC, Lee CA, eds. Oxford, UK: Blackwell
-
Oldenberg J, Tuddenham E. Genetic basis of inhibitor development in severe hemophilia A and B. In: Rodriguez-Merchan EC, Lee CA, eds. Inhibitors in Patients with Haemophilia. Oxford, UK: Blackwell; 2002:21-26.
-
(2002)
Inhibitors in Patients with Haemophilia
, pp. 21-26
-
-
Oldenberg, J.1
Tuddenham, E.2
-
25
-
-
6644227418
-
The Malmö International Brother Study (MIBS): Further support for genetic predisposition to inhibitor development in hemophilia patients
-
Astermark J, Berntorp E, White GC, Kroner BL, for the MIBS Study Group. The Malmö International Brother Study (MIBS): further support for genetic predisposition to inhibitor development in hemophilia patients. Haemophilia. 2001;7:267-272.
-
(2001)
Haemophilia
, vol.7
, pp. 267-272
-
-
Astermark, J.1
Berntorp, E.2
White, G.C.3
Kroner, B.L.4
-
26
-
-
0000939750
-
Increased frequency of inhibitors in African American hemophilia A patients
-
Addiego JR Jr, Kasper C, Abildgaard C, et al. Increased frequency of inhibitors in African American hemophilia A patients [abstract]. Blood. 1994;84(suppl 1):239a.
-
(1994)
Blood
, vol.84
, Issue.SUPPL. 1
-
-
Addiego Jr., J.R.1
Kasper, C.2
Abildgaard, C.3
-
27
-
-
0034994489
-
Incidence of factor VIII inhibitors in severe hemophilia: The importance of patient age
-
Lorenzo JI, Lopez A, Altisent C, Aznar JA. Incidence of factor VIII inhibitors in severe hemophilia: the importance of patient age. Br J Haematol. 2001;113:600-603.
-
(2001)
Br J Haematol
, vol.113
, pp. 600-603
-
-
Lorenzo, J.I.1
Lopez, A.2
Altisent, C.3
Aznar, J.A.4
-
28
-
-
0842333021
-
Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia A
-
Sharathkumar A, Lillicrap D, Blanchette VS, et al. Intensive exposure to factor VIII is a risk factor for inhibitor development in mild hemophilia A. J Thromb Haemost. 2003;1:1228-1236.
-
(2003)
J Thromb Haemost
, vol.1
, pp. 1228-1236
-
-
Sharathkumar, A.1
Lillicrap, D.2
Blanchette, V.S.3
-
29
-
-
0036044248
-
Inhibitors in the Swedish population with severe haemophilia A and B: A 20-year survey
-
Knobel KE, Sjorin E, Tengborn LI, Petrini P, Ljung RC. Inhibitors in the Swedish population with severe haemophilia A and B: a 20-year survey. Acta Paediatr. 2002;91:910-914.
-
(2002)
Acta Paediatr
, vol.91
, pp. 910-914
-
-
Knobel, K.E.1
Sjorin, E.2
Tengborn, L.I.3
Petrini, P.4
Ljung, R.C.5
-
30
-
-
11044223880
-
Effect of type of treatment (recombinant vs. plasmatic) on FVIII inhibitor incidence according to known risk cofactors in previously untreated severe hemophilia A patients (PUPs)
-
Abstract OC215
-
Rothschild C, Goudemand J, Demiguel V, Lambert T, Calvez T. Effect of type of treatment (recombinant vs. plasmatic) on FVIII inhibitor incidence according to known risk cofactors in previously untreated severe hemophilia A patients (PUPs) [abstract]. J Thromb Haemost. 2003;1(suppl). Abstract OC215.
-
(2003)
J Thromb Haemost
, vol.1
, Issue.SUPPL.
-
-
Rothschild, C.1
Goudemand, J.2
Demiguel, V.3
Lambert, T.4
Calvez, T.5
-
31
-
-
0036332175
-
Von Willebrand factor modulates factor VIII immunogenicity: Comparative study of different factor VIII concentrates in a hemophilia A mouse model
-
Behrmann M, Pasi J, Saint-Remy JM, Kotitschke R, Kloft M. Von Willebrand factor modulates factor VIII immunogenicity: comparative study of different factor VIII concentrates in a hemophilia A mouse model. Thromb Haemost. 2002;88:221-229.
-
(2002)
Thromb Haemost
, vol.88
, pp. 221-229
-
-
Behrmann, M.1
Pasi, J.2
Saint-Remy, J.M.3
Kotitschke, R.4
Kloft, M.5
-
32
-
-
0025847974
-
The design and analysis of half-life and recovery studies for factor VIII and factor IX: Factor VIII/Factor IX Scientific and Standardization Committee of the International Society for Thrombosis and Haemostasis
-
Morfini M, Lee M, Messori A. The design and analysis of half-life and recovery studies for factor VIII and factor IX: Factor VIII/Factor IX Scientific and Standardization Committee of the International Society for Thrombosis and Haemostasis. Thromb Haemost. 1991;66:384-386.
-
(1991)
Thromb Haemost
, vol.66
, pp. 384-386
-
-
Morfini, M.1
Lee, M.2
Messori, A.3
-
34
-
-
0038825162
-
Continuous infusion
-
Schulman S. Continuous infusion. Haemophilia. 2003;9:368-375.
-
(2003)
Haemophilia
, vol.9
, pp. 368-375
-
-
Schulman, S.1
-
35
-
-
0021067681
-
Autoplex versus Proplex: A controlled, double-blind study of effectiveness in acute hemarthroses in hemophiliacs with inhibitors to factor VIII
-
Lusher JM, Blatt PM, Penner JA, et al. Autoplex versus Proplex: a controlled, double-blind study of effectiveness in acute hemarthroses in hemophiliacs with inhibitors to factor VIII. Blood. 1983;62:1135-1138.
-
(1983)
Blood
, vol.62
, pp. 1135-1138
-
-
Lusher, J.M.1
Blatt, P.M.2
Penner, J.A.3
-
36
-
-
11044234839
-
FEIBA: Mode of action
-
Turecek PL, Varadi K, Gritsch H, Schwarz HP. FEIBA: mode of action. Haemophilia. 2004;10(suppl 2):3-9.
-
(2004)
Haemophilia
, vol.10
, Issue.SUPPL. 2
, pp. 3-9
-
-
Turecek, P.L.1
Varadi, K.2
Gritsch, H.3
Schwarz, H.P.4
-
37
-
-
0030837755
-
Multicenter retrospective study on the utilization of FEIBA in France in patients with factor VIII and factor IX inhibitors. French FEIBA Study Group. Factor Eight Bypassing Activity
-
Negrier C, Goudemand J, Sultan Y, Bertrand M, Rothschild C, Lauroua P. Multicenter retrospective study on the utilization of FEIBA in France in patients with factor VIII and factor IX inhibitors. French FEIBA Study Group. Factor Eight Bypassing Activity. Thromb Haemost. 1997;77:1113-1119.
-
(1997)
Thromb Haemost
, vol.77
, pp. 1113-1119
-
-
Negrier, C.1
Goudemand, J.2
Sultan, Y.3
Bertrand, M.4
Rothschild, C.5
Lauroua, P.6
-
38
-
-
0038441421
-
Long-term FEIBA prophylaxis does not prevent progression of existing joint disease
-
Hilgartner MW, Makipernaa A, DiMichele DM. Long-term FEIBA prophylaxis does not prevent progression of existing joint disease. Haemophilia. 2003;9:261-268.
-
(2003)
Haemophilia
, vol.9
, pp. 261-268
-
-
Hilgartner, M.W.1
Makipernaa, A.2
Dimichele, D.M.3
-
39
-
-
0030056318
-
Immune tolerance for the treatment of FVIII inhibitors: Twenty years of the Bonn protocol
-
Brackmann HH, Oldenberg J, Schwaab R. Immune tolerance for the treatment of FVIII inhibitors: twenty years of the Bonn protocol. Vox Sang. 1996;70(suppl 1):30-35.
-
(1996)
Vox Sang
, vol.70
, Issue.SUPPL. 1
, pp. 30-35
-
-
Brackmann, H.H.1
Oldenberg, J.2
Schwaab, R.3
-
40
-
-
0035200558
-
The action of high-dose factor VIIa (FVIIa) in a cell-based model of hemostasis
-
Hoffman M, Monroe DM III. The action of high-dose factor VIIa (FVIIa) in a cell-based model of hemostasis. Semin Hematol. 2001;38:6-9.
-
(2001)
Semin Hematol
, vol.38
, pp. 6-9
-
-
Hoffman, M.1
Monroe III, D.M.2
-
41
-
-
0036090268
-
Inhibition of fibrinolysis by recombinant factor VIIa in plasma from patients with severe hemophilia A
-
Lisman T, Mosnier LO, Lambert T, et al. Inhibition of fibrinolysis by recombinant factor VIIa in plasma from patients with severe hemophilia A. Blood. 2002;99:175-179.
-
(2002)
Blood
, vol.99
, pp. 175-179
-
-
Lisman, T.1
Mosnier, L.O.2
Lambert, T.3
-
42
-
-
0029966655
-
Recombinant factor VIIa in joint and muscle bleeding episodes
-
Bech RM. Recombinant factor VIIa in joint and muscle bleeding episodes. Haemostasis. 1996;26(suppl 1):135-138.
-
(1996)
Haemostasis
, vol.26
, Issue.SUPPL. 1
, pp. 135-138
-
-
Bech, R.M.1
-
43
-
-
0031743928
-
A randomized, double-blind comparison of two dosage levels of recombinant factor VIIa in the treatment of joint, muscle and mucocutaneous haemorrhages in persons with haemophilia A and B, with and without inhibitors: RFVIIa Study Group
-
Lusher JM, Roberts HR, Davignon G, et al. A randomized, double-blind comparison of two dosage levels of recombinant factor VIIa in the treatment of joint, muscle and mucocutaneous haemorrhages in persons with haemophilia A and B, with and without inhibitors: rFVIIa Study Group. Haemophilia. 1998;4:790-798.
-
(1998)
Haemophilia
, vol.4
, pp. 790-798
-
-
Lusher, J.M.1
Roberts, H.R.2
Davignon, G.3
-
44
-
-
17144437423
-
Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (NovoSeven) in hemophiliacs with inhibitors
-
Key NS, Aledort LM, Beardsley D, et al. Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (NovoSeven) in hemophiliacs with inhibitors. Thromb Haemost. 1998;80:912-918.
-
(1998)
Thromb Haemost
, vol.80
, pp. 912-918
-
-
Key, N.S.1
Aledort, L.M.2
Beardsley, D.3
-
45
-
-
0034129960
-
Acute hemarthroses: The benefits of early versus late treatment with recombinant activated factor VII
-
Lusher JM. Acute hemarthroses: the benefits of early versus late treatment with recombinant activated factor VII. Blood Coagul Fibrinolysis. 2000;11(suppl 1):S45-S49.
-
(2000)
Blood Coagul Fibrinolysis
, vol.11
, Issue.SUPPL. 1
-
-
Lusher, J.M.1
-
46
-
-
0031743504
-
Prospective, randomised trial of two doses of rFVIIa (NovoSeven) in haemophilia patients with inhibitors undergoing surgery
-
Shapiro AD, Gilchrist GS, Hoots WK, Cooper HA, Gastineau DA. Prospective, randomised trial of two doses of rFVIIa (NovoSeven) in haemophilia patients with inhibitors undergoing surgery. Thromb Haemost. 1998;80:773-778.
-
(1998)
Thromb Haemost
, vol.80
, pp. 773-778
-
-
Shapiro, A.D.1
Gilchrist, G.S.2
Hoots, W.K.3
Cooper, H.A.4
Gastineau, D.A.5
-
47
-
-
9044244906
-
Major surgery in haemophilic patients with inhibitors using recombinant factor VIIa
-
Ingerslev J, Freidman D, Gastineau D, et al. Major surgery in haemophilic patients with inhibitors using recombinant factor VIIa. Hemostasis. 1996;26:118-123.
-
(1996)
Hemostasis
, vol.26
, pp. 118-123
-
-
Ingerslev, J.1
Freidman, D.2
Gastineau, D.3
-
48
-
-
0031759475
-
Experiences with continuous infusion of recombinant activated factor VII
-
Schulman S, d'Oiron R, Martinowitz U, et al. Experiences with continuous infusion of recombinant activated factor VII. Blood Coagul Fibrinolysis. 1998;9(suppl 1):S97-S101.
-
(1998)
Blood Coagul Fibrinolysis
, vol.9
, Issue.SUPPL. 1
-
-
Schulman, S.1
D'Oiron, R.2
Martinowitz, U.3
-
49
-
-
0035199305
-
Inhibitor treatment: State of the art
-
Shapiro A. Inhibitor treatment: state of the art. Semin Hematol. 2001;38:26-34.
-
(2001)
Semin Hematol
, vol.38
, pp. 26-34
-
-
Shapiro, A.1
-
50
-
-
0642372623
-
A new approach to treatment of bleeding episodes in young hemophilia patients: A single bolus megadose of recombinant activated factor VII (Novo-Seven)
-
Kenet G, Lubetsky A, Luboshitz J, Martinowitz U. A new approach to treatment of bleeding episodes in young hemophilia patients: a single bolus megadose of recombinant activated factor VII (Novo-Seven). J Thromb Haemost. 2003;1:450-455.
-
(2003)
J Thromb Haemost
, vol.1
, pp. 450-455
-
-
Kenet, G.1
Lubetsky, A.2
Luboshitz, J.3
Martinowitz, U.4
-
51
-
-
0035200558
-
The action of high-dose factor VIIa (FVIIa) in a cell-based model of hemostasis
-
Hoffman M, Monroe DM 3rd. The action of high-dose factor VIIa (FVIIa) in a cell-based model of hemostasis. Semin Hematol. 2001;38(suppl 12):6-9.
-
(2001)
Semin Hematol
, vol.38
, Issue.SUPPL. 12
, pp. 6-9
-
-
Hoffman, M.1
Monroe III, D.M.2
-
52
-
-
0036489638
-
Safety of factor VIII inhibitor bypass activity (FEIBA): 10-Year compilation of thrombotic adverse events
-
Ehrlich HJ, Henzl MJ, Gomperts ED. Safety of factor VIII inhibitor bypass activity (FEIBA): 10-year compilation of thrombotic adverse events. Haemophilia. 2002;8:83-90.
-
(2002)
Haemophilia
, vol.8
, pp. 83-90
-
-
Ehrlich, H.J.1
Henzl, M.J.2
Gomperts, E.D.3
-
53
-
-
19044365519
-
The evidence behind inhibitor treatment with recombinant factor VIIa
-
Ludlam CA. The evidence behind inhibitor treatment with recombinant factor VIIa. Pathophysiol Haemost Thromb. 2002:32(suppl 1):13-18.
-
(2002)
Pathophysiol Haemost Thromb
, vol.32
, Issue.SUPPL. 1
, pp. 13-18
-
-
Ludlam, C.A.1
-
54
-
-
0035543815
-
Total thrombin-activatable fibrinolysis inhibitor (TAFI) antigen and pro-TAFI in patients with haemophilia A
-
Antovic J, Schulman S, Eelde A, Blomback M. Total thrombin-activatable fibrinolysis inhibitor (TAFI) antigen and pro-TAFI in patients with haemophilia A. Haemophilia. 2001;7:557-560.
-
(2001)
Haemophilia
, vol.7
, pp. 557-560
-
-
Antovic, J.1
Schulman, S.2
Eelde, A.3
Blomback, M.4
-
55
-
-
0035170866
-
Immune tolerance in haemophilia with factor VIII inhibitors: Predictors of success
-
Mariani G, Kroner B, and the Immune Tolerance Study Group (ITSG). Immune tolerance in haemophilia with factor VIII inhibitors: predictors of success. Haematologica. 2001;86:1186-1193.
-
(2001)
Haematologica
, vol.86
, pp. 1186-1193
-
-
Mariani, G.1
Kroner, B.2
-
56
-
-
0035130887
-
Treatment of coagulation inhibitors with extracorporeal immunoadsorption (Ig-Therasorb)
-
Jansen M, Schmaldienst S, Banyai S, et al. Treatment of coagulation inhibitors with extracorporeal immunoadsorption (Ig-Therasorb). Br J Haematol. 2001;112:91-97.
-
(2001)
Br J Haematol
, vol.112
, pp. 91-97
-
-
Jansen, M.1
Schmaldienst, S.2
Banyai, S.3
-
57
-
-
0017785868
-
Massive factor-VIII infusion in haemophiliac with factor-VIII inhibitor, high responder
-
Brackmann HH, Gormsen J. Massive factor-VIII infusion in haemophiliac with factor-VIII inhibitor, high responder. Lancet. 1977;2:933,
-
(1977)
Lancet
, vol.2
, pp. 933
-
-
Brackmann, H.H.1
Gormsen, J.2
-
59
-
-
0033694596
-
The maintenance of tolerance after successful immune tolerance induction in hemophilia A and B: The North American Registry
-
DiMichele D, Kroner B, and the Factor VIII/IX Subcommittee of the International Society for Thrombosis and Hemostasis. The maintenance of tolerance after successful immune tolerance induction in hemophilia A and B: the North American Registry. Haematologica. 2000;85(suppl):42-44.
-
(2000)
Haematologica
, vol.85
, Issue.SUPPL.
, pp. 42-44
-
-
DiMichele, D.1
Kroner, B.2
-
60
-
-
0028411947
-
Immunetolerance as treatment of alloantibodies to factor VIII in hemophilia: The International Registry of Immunetolerance Protocols
-
Mariani G, Scheibel E, Nogao T, et al. Immunetolerance as treatment of alloantibodies to factor VIII in hemophilia: the International Registry of Immunetolerance Protocols. Semin Hematol. 1994;31:62-64.
-
(1994)
Semin Hematol
, vol.31
, pp. 62-64
-
-
Mariani, G.1
Scheibel, E.2
Nogao, T.3
-
61
-
-
0033678959
-
The German Registry of immune tolerance treatment in hemophilia: 1999 Update
-
Lenk H, and the ITT Study Group. The German Registry of immune tolerance treatment in hemophilia: 1999 update. Haematologica. 2000;85(suppl):45-47.
-
(2000)
Haematologica
, vol.85
, Issue.SUPPL.
, pp. 45-47
-
-
Lenk, H.1
-
62
-
-
0036147943
-
The North American Immune Tolerance Registry: Practices, outcomes, outcome predictors
-
DiMichele DM, Kroner B, and the North American Immune Tolerance Study Group. The North American Immune Tolerance Registry: practices, outcomes, outcome predictors. Thromb Haemost. 2002;87:52-57.
-
(2002)
Thromb Haemost
, vol.87
, pp. 52-57
-
-
DiMichele, D.M.1
Kroner, B.2
-
63
-
-
0037710764
-
Immune tolerance: A synopsis of the international experience
-
DiMichele DM. Immune tolerance: a synopsis of the international experience. Haemophilia. 1998;4:568-573.
-
(1998)
Haemophilia
, vol.4
, pp. 568-573
-
-
DiMichele, D.M.1
-
64
-
-
0032882450
-
Comparison of the International Immune Tolerance Registry and the North American Immune Tolerance Registry
-
Kroner BL. Comparison of the International Immune Tolerance Registry and the North American Immune Tolerance Registry. Vox Sang. 1999;77(suppl 1):33-37.
-
(1999)
Vox Sang
, vol.77
, Issue.SUPPL. 1
, pp. 33-37
-
-
Kroner, B.L.1
-
65
-
-
0038779219
-
Central venous lines in haemophilia
-
Ljung R. Central venous lines in haemophilia. Haemophilia. 2003;9(suppl 1):88-93.
-
(2003)
Haemophilia
, vol.9
, Issue.SUPPL. 1
, pp. 88-93
-
-
Ljung, R.1
-
66
-
-
0031958313
-
FVIII inhibitors in mild and moderate-severity haemophilia A: UK Haemophilia Centre Directors Organisation
-
Hay CR, Ludlam CA, Colvin BT, et al. FVIII inhibitors in mild and moderate-severity haemophilia A: UK Haemophilia Centre Directors Organisation. Thromb Haemost. 1998;79:762-766.
-
(1998)
Thromb Haemost
, vol.79
, pp. 762-766
-
-
Hay, C.R.1
Ludlam, C.A.2
Colvin, B.T.3
-
67
-
-
0033041458
-
Tolerance induction using the Malmö treatment model 1982-1995
-
Freiburghaus C, Berntorp E, Ekman M, Gunnarsson M, Kjellberg B, Nilsson IM. Tolerance induction using the Malmö treatment model 1982-1995. Haemophilia. 1999;5:32-39.
-
(1999)
Haemophilia
, vol.5
, pp. 32-39
-
-
Freiburghaus, C.1
Berntorp, E.2
Ekman, M.3
Gunnarsson, M.4
Kjellberg, B.5
Nilsson, I.M.6
-
68
-
-
2942591961
-
Selective B-cell depletion with rituximab for the treatment of patients with acquired hemophilia
-
Stasi R, Brunetti M, Stipa E, Amadori S. Selective B-cell depletion with rituximab for the treatment of patients with acquired hemophilia. Blood. 2004;103:4424-4428.
-
(2004)
Blood
, vol.103
, pp. 4424-4428
-
-
Stasi, R.1
Brunetti, M.2
Stipa, E.3
Amadori, S.4
-
69
-
-
2442472195
-
Rituximab in the treatment of alloimmune factor VIII and IX antibodies in two children with severe haemophilia
-
Mathias M, Khair K, Hann I, Liesner R. Rituximab in the treatment of alloimmune factor VIII and IX antibodies in two children with severe haemophilia. Br J Haematol. 2004;125:366-368.
-
(2004)
Br J Haematol
, vol.125
, pp. 366-368
-
-
Mathias, M.1
Khair, K.2
Hann, I.3
Liesner, R.4
-
70
-
-
0034651022
-
Reduction of the antigenicity of factor VIII toward complex inhibitory antibody plasmas using multiply-substituted hybrid human/porcine factor VIII molecules
-
Barrow RT, Healey JF, Gailani D, et al. Reduction of the antigenicity of factor VIII toward complex inhibitory antibody plasmas using multiply-substituted hybrid human/porcine factor VIII molecules. Blood. 2000;95:564-568.
-
(2000)
Blood
, vol.95
, pp. 564-568
-
-
Barrow, R.T.1
Healey, J.F.2
Gailani, D.3
-
71
-
-
0042243611
-
Peptide decoys selected by phage display block in vitro and in vivo activity of a human anti-FVIII inhibitor
-
Villard S, Lacroix-Desmazes S, Kieber-Emmons T, et al. Peptide decoys selected by phage display block in vitro and in vivo activity of a human anti-FVIII inhibitor. Blood. 2003;102:949-952.
-
(2003)
Blood
, vol.102
, pp. 949-952
-
-
Villard, S.1
Lacroix-Desmazes, S.2
Kieber-Emmons, T.3
-
73
-
-
0032510756
-
Genetic induction of immune tolerance to human clotting factor VIII in a mouse model for hemophilia A
-
Evans GL, Morgan RA. Genetic induction of immune tolerance to human clotting factor VIII in a mouse model for hemophilia A. Proc Natl Acad Sci U S A. 1998;95:5734-5739.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 5734-5739
-
-
Evans, G.L.1
Morgan, R.A.2
-
74
-
-
0033678464
-
Immune tolerance induction and the treatment of hemophilia: Malmö protocol update
-
Berntorp E, Astermark J, Carlborg E. Immune tolerance induction and the treatment of hemophilia: Malmö protocol update. Haematologica. 2000;85(suppl):48-51.
-
(2000)
Haematologica
, vol.85
, Issue.SUPPL.
, pp. 48-51
-
-
Berntorp, E.1
Astermark, J.2
Carlborg, E.3
-
75
-
-
0033041458
-
Tolerance induction using the Malmo treatment model 1982-1995
-
Freiburghaus C, Berntorp E, Eckman M, et al. Tolerance induction using the Malmo treatment model 1982-1995. Haemophilia. 1999;5:32-39.
-
(1999)
Haemophilia
, vol.5
, pp. 32-39
-
-
Freiburghaus, C.1
Berntorp, E.2
Eckman, M.3
-
76
-
-
0032949524
-
Immune tolerance therapy for hemophilia A patients with acquired factor VIII alloantibodies: Comprehensive analysis of experience at a single institution
-
Smith MP, Spence KJ, Waters EL, et al. Immune tolerance therapy for hemophilia A patients with acquired factor VIII alloantibodies: comprehensive analysis of experience at a single institution. Thromb Haemost. 1999;81:35-38.
-
(1999)
Thromb Haemost
, vol.81
, pp. 35-38
-
-
Smith, M.P.1
Spence, K.J.2
Waters, E.L.3
-
77
-
-
0035135212
-
Immune tolerance induction in hemophilia A patients with high-responding inhibitors to factor VIII: Experiecne at a single institution
-
Rocino A, Papa ML, Salerno E, et al. Immune tolerance induction in hemophilia A patients with high-responding inhibitors to factor VIII: experiecne at a single institution. Hemophilia. 2001;7:33-38.
-
(2001)
Hemophilia
, vol.7
, pp. 33-38
-
-
Rocino, A.1
Papa, M.L.2
Salerno, E.3
-
78
-
-
0028244702
-
Clinical course of factor VIII inhibitors developed after exposure to a pasteurised Dutch concentrate compared to classic inhibitors in hemophilia A
-
Mauser-Bunschoten EP, Rosendaal FR, Nieuwenhuis HK, et al. Clinical course of factor VIII inhibitors developed after exposure to a pasteurised Dutch concentrate compared to classic inhibitors in hemophilia A. Thromb Haemost. 1994;71:703-706.
-
(1994)
Thromb Haemost
, vol.71
, pp. 703-706
-
-
Mauser-Bunschoten, E.P.1
Rosendaal, F.R.2
Nieuwenhuis, H.K.3
-
79
-
-
0026571955
-
Induction of immune tolerance in patients with hemophilia A and inhibitors
-
Gruppo RA, Valdez LP, Stout RD. Induction of immune tolerance in patients with hemophilia A and inhibitors. Am J Pediatr Hematol Oncol. 1992;14:82-87.
-
(1992)
Am J Pediatr Hematol Oncol
, vol.14
, pp. 82-87
-
-
Gruppo, R.A.1
Valdez, L.P.2
Stout, R.D.3
|