-
1
-
-
33645957674
-
Variant Creutzfeldt-Jakob disease: Risk of transmission by blood transfusion and blood therapies
-
Ironside JW. Variant Creutzfeldt-Jakob disease: Risk of transmission by blood transfusion and blood therapies. Haemophilia 2006; 12 (Suppl. 1): 8-15.
-
(2006)
, vol.12
, pp. 8-15
-
-
Ironside, J.W.1
-
2
-
-
0028132226
-
Biology and genetics of prion diseases
-
Prusiner SB. Biology and genetics of prion diseases. Annu Rev Microbiol 1994; 48: 655-86.
-
(1994)
, vol.48
, pp. 655-686
-
-
Prusiner, S.B.1
-
3
-
-
0141737854
-
Bovine spongiform encephalopathy (BSE) and its epidemiology
-
Smith PG, Bradley R. Bovine spongiform encephalopathy (BSE) and its epidemiology. Br Med Bull 2003; 66: 185-98.
-
(2003)
, vol.66
, pp. 185-198
-
-
Smith, P.G.1
Bradley, R.2
-
4
-
-
4043048783
-
Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies
-
Priola SA, Vorberg I. Molecular aspects of disease pathogenesis in the transmissible spongiform encephalopathies. Methods Mol Biol 2004; 268: 517-40.
-
(2004)
, vol.268
, pp. 517-540
-
-
Priola, S.A.1
Vorberg, I.2
-
5
-
-
33646228928
-
Diagnosis and management of inhibitors to factors VIII and IX. An introductory discussion for physicians
-
no. 34
-
Kasper CK. Diagnosis and management of inhibitors to factors VIII and IX. An introductory discussion for physicians. In: Treatment of Hemophilia. September, 2004. no. 34.
-
(2004)
-
-
Kasper, C.K.1
-
6
-
-
9144271883
-
The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99
-
Darby SC, Keeling DM, Spooner RJ et.al. The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99. J Thromb Haemost 2004; 2: 1047-54.
-
(2004)
, vol.2
, pp. 1047-1054
-
-
Darby, S.C.1
Keeling, D.M.2
Spooner, R.J.3
-
7
-
-
0038383604
-
Immune tolerance induction in patients with haemophilia A with inhibitors: A systematic review
-
Wight J, Paisley S, Knight C. Immune tolerance induction in patients with haemophilia A with inhibitors: A systematic review. Haemophilia 2003; 9: 436-63.
-
(2003)
, vol.9
, pp. 436-463
-
-
Wight, J.1
Paisley, S.2
Knight, C.3
-
8
-
-
0842342601
-
Environmental and genetic factors influencing inhibitor development
-
Oldenburg J, Schroder J, Brackmann HH, Muller-Reible C, Schwaab R, Tuddenham E. Environmental and genetic factors influencing inhibitor development. Semin Hematol 2004; 41: 82-8.
-
(2004)
, vol.41
, pp. 82-88
-
-
Oldenburg, J.1
Schroder, J.2
Brackmann, H.H.3
Muller-Reible, C.4
Schwaab, R.5
Tuddenham, E.6
-
9
-
-
6644227418
-
The Malmo International Brother Study (MIBS): Further support for genetic predisposition to inhibitor development in hemophilia patients
-
Astermark J, Berntorp E, White GC, Kroner BL. The Malmo International Brother Study (MIBS): Further support for genetic predisposition to inhibitor development in hemophilia patients. Haemophilia 2001; 7: 267-72.
-
(2001)
, vol.7
, pp. 267-272
-
-
Astermark, J.1
Berntorp, E.2
White, G.C.3
Kroner, B.L.4
-
10
-
-
0027473752
-
Recombinant factor VIII for the treatment of previously untreated patients with hemophilia A. Safety, efficacy, and development of inhibitors. Kogenate Previously Untreated Patient Study Group
-
Lusher JM, Arkin S, Abildgaard CF, Schwartz RS. Recombinant factor VIII for the treatment of previously untreated patients with hemophilia A. Safety, efficacy, and development of inhibitors. Kogenate Previously Untreated Patient Study Group. N Engl J Med 1993; 328: 453-9.
-
(1993)
, vol.328
, pp. 453-459
-
-
Lusher, J.M.1
Arkin, S.2
Abildgaard, C.F.3
Schwartz, R.S.4
-
11
-
-
33845239946
-
Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A
-
Astermark J, Oldenburg J, Carlson J et.al. Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A. Blood 2006; 108: 3739-45.
-
(2006)
, vol.108
, pp. 3739-3745
-
-
Astermark, J.1
Oldenburg, J.2
Carlson, J.3
-
12
-
-
33645751563
-
Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A
-
Astermark J, Oldenburg J, Pavlova A, Berntorp E, Lefvert AK. Polymorphisms in the IL10 but not in the IL1beta and IL4 genes are associated with inhibitor development in patients with hemophilia A. Blood 2006; 107: 3167-72.
-
(2006)
, vol.107
, pp. 3167-3172
-
-
Astermark, J.1
Oldenburg, J.2
Pavlova, A.3
Berntorp, E.4
Lefvert, A.K.5
-
13
-
-
33846420672
-
Polymorphisms in the CTLA-4 gene and inhibitor development in patients with severe hemophilia A
-
Astermark J, Wang X, Oldenburg J, Berntorp E, Lefvert AK. Polymorphisms in the CTLA-4 gene and inhibitor development in patients with severe hemophilia A. J Thromb Haemost 2007; 5: 263-5.
-
(2007)
, vol.5
, pp. 263-265
-
-
Astermark, J.1
Wang, X.2
Oldenburg, J.3
Berntorp, E.4
Lefvert, A.K.5
-
14
-
-
0034994489
-
Incidence of factor VIII inhibitors in severe haemophilia: The importance of patient age
-
Lorenzo JI, Lopez A, Altisent C, Aznar JA. Incidence of factor VIII inhibitors in severe haemophilia: The importance of patient age. Br J Haematol 2001; 113: 600-3.
-
(2001)
, vol.113
, pp. 600-603
-
-
Lorenzo, J.I.1
Lopez, A.2
Altisent, C.3
Aznar, J.A.4
-
15
-
-
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: 1228-36.
-
(2003)
, vol.1
, pp. 1228-1236
-
-
Sharathkumar, A.1
Lillicrap, D.2
Blanchette, V.S.3
-
16
-
-
25444445056
-
Inhibitor development in patients with hemophilia A after continuous infusion of FVIII concentrates
-
von Auer C, Oldenburg J, von Depka M et.al. Inhibitor development in patients with hemophilia A after continuous infusion of FVIII concentrates. Ann N Y Acad Sci 2005; 1051: 498-505.
-
(2005)
, vol.1051
, pp. 498-505
-
-
von Auer, C.1
Oldenburg, J.2
von Depka, M.3
-
17
-
-
34250708408
-
Treatment characteristics and the risk of inhibitor development: A multi-center cohort study among previously untreated patients with severe hemophilia A
-
Gouw SC, van den Berg HM, le Cessie S, van der Bom JG. Treatment characteristics and the risk of inhibitor development: A multi-center cohort study among previously untreated patients with severe hemophilia A. J Thromb Haemost 2007; 5: 1383-90.
-
(2007)
, vol.5
, pp. 1383-1390
-
-
Gouw, S.C.1
van den Berg, H.M.2
le Cessie, S.3
van der Bom, J.G.4
-
18
-
-
33644885734
-
Protective effect of prophylaxis on inhibitor development in children with hemophilia A: More convincing studies are required. Response to Calvez and Laurian
-
Santagostino E, Mannucci PM. Protective effect of prophylaxis on inhibitor development in children with hemophilia A: More convincing studies are required. Response to Calvez and Laurian. Br J Haematol 2006; 132: 800-1.
-
(2006)
, vol.132
, pp. 800-801
-
-
Santagostino, E.1
Mannucci, P.M.2
-
19
-
-
33846922841
-
Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A
-
Chalmers EA, Brown SA, Keeling D et.al. Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A. Haemophilia 2007; 13: 149-55.
-
(2007)
, vol.13
, pp. 149-155
-
-
Chalmers, E.A.1
Brown, S.A.2
Keeling, D.3
-
20
-
-
30344434999
-
Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A
-
Goudemand J, Rothschild C, Demiguel V et.al. Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A. Blood 2006; 107: 46-51.
-
(2006)
, vol.107
, pp. 46-51
-
-
Goudemand, J.1
Rothschild, C.2
Demiguel, V.3
-
21
-
-
33846244931
-
VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors
-
Dasgupta S, Repesse Y, Bayry J et.al. VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors. Blood 2007; 109: 610-2.
-
(2007)
, vol.109
, pp. 610-612
-
-
Dasgupta, S.1
Repesse, Y.2
Bayry, J.3
-
22
-
-
4844227035
-
Relationships between factor VIII:Ag and factor VIII in recombinant and plasma-derived factor VIII concentrates
-
Lin Y, Yang X, Chevrier MC et.al. Relationships between factor VIII:AG and factor VIII in recombinant and plasma-derived factor VIII concentrates. Haemophilia 2004; 10: 459-69.
-
(2004)
, vol.10
, pp. 459-469
-
-
Lin, Y.1
Yang, X.2
Chevrier, M.C.3
-
23
-
-
3042576416
-
The factor VIII/von Willebrand factor complex: Basic and clinical issues
-
Federici AB. The factor VIII/von Willebrand factor complex: Basic and clinical issues. Haematologica 2003; 88: EREP02.
-
(2003)
, vol.88
-
-
Federici, A.B.1
-
24
-
-
0036147943
-
The North American Immune Tolerance Registry: Practices, outcomes, outcome predictors
-
DiMichele DM, Kroner BL. The North American Immune Tolerance Registry: practices, outcomes, outcome predictors. Thromb Haemost 2002; 87: 52-7.
-
(2002)
, vol.87
, pp. 52-57
-
-
DiMichele, D.M.1
Kroner, B.L.2
-
25
-
-
0032836833
-
International Immune Tolerance Registry, 1997 update
-
Mariani G, Kroner B. International Immune Tolerance Registry, 1997 update. Vox Sang 1999; 77 (Suppl. 1): 25-7.
-
(1999)
, vol.77
, pp. 25-27
-
-
Mariani, G.1
Kroner, B.2
-
26
-
-
2542560221
-
The role of plasma-derived factor VIII/von Willebrand factor concentrates in the treatment of hemophilia A patients
-
Auerswald G, Spranger T, Brackmann HH. The role of plasma-derived factor VIII/von Willebrand factor concentrates in the treatment of hemophilia A patients. Haematologica 2003; 88: EREP05.
-
(2003)
, vol.88
-
-
Auerswald, G.1
Spranger, T.2
Brackmann, H.H.3
-
27
-
-
19944394681
-
Immune tolerance induction in haemophilia A patients with inhibitors: The choice of concentrate affecting success
-
Kreuz W, Escuriola-Ettingshausen C, Auerswald G. Immune tolerance induction in haemophilia A patients with inhibitors: The choice of concentrate affecting success. Haematologica 2001; 86 (Suppl. 4): 16-20.
-
(2001)
, vol.86
, pp. 16-20
-
-
Kreuz, W.1
Escuriola-Ettingshausen, C.2
Auerswald, G.3
-
28
-
-
25444521967
-
Immune tolerance induction with highly purified plasma-derived factor VIII containing von Willebrand factor in hemophilia A patients with high-responding inhibitors
-
Orsini F, Rothschild C, Beurrier P, Faradji A, Goudemand J, Polack B. Immune tolerance induction with highly purified plasma-derived factor VIII containing von Willebrand factor in hemophilia A patients with high-responding inhibitors. Haematologica 2005; 90: 1288-90.
-
(2005)
, vol.90
, pp. 1288-1290
-
-
Orsini, F.1
Rothschild, C.2
Beurrier, P.3
Faradji, A.4
Goudemand, J.5
Polack, B.6
-
29
-
-
34447287337
-
Immune tolerance induction with a high purity von Willebrand factor/VIII complex concentrate in haemophilia A patients with inhibitors at high risk of a poor response
-
Gringeri A, Musso R, Mazzucconi MG et.al. Immune tolerance induction with a high purity von Willebrand factor/VIII complex concentrate in haemophilia A patients with inhibitors at high risk of a poor response. Haemophilia 2007; 13: 373-9.
-
(2007)
, vol.13
, pp. 373-379
-
-
Gringeri, A.1
Musso, R.2
Mazzucconi, M.G.3
-
30
-
-
0036332175
-
Von Willebrand factor modulates factor VIII immunogenicity: Comparative study of different factor VIII concentrates in a haemophilia 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 haemophilia A mouse model. Thromb Haemost 2002; 88: 221-9.
-
(2002)
, vol.88
, pp. 221-229
-
-
Behrmann, M.1
Pasi, J.2
Saint-Remy, J.M.3
Kotitschke, R.4
Kloft, M.5
-
31
-
-
0030044206
-
Immune tolerance and the immune modulation protocol
-
Berntorp E, Nilsson IM. Immune tolerance and the immune modulation protocol. Vox Sang 1996; 70 (Suppl. 1): 36-41.
-
(1996)
, vol.70
, pp. 36-41
-
-
Berntorp, E.1
Nilsson, I.M.2
-
32
-
-
0034917040
-
von Willebrand factor in factor VIII concentrates protects against neutralization by factor VIII antibodies of haemophilia A patients
-
Kallas A, Talpsep T. von Willebrand factor in factor VIII concentrates protects against neutralization by factor VIII antibodies of haemophilia A patients. Haemophilia 2001; 7: 375-80.
-
(2001)
, vol.7
, pp. 375-380
-
-
Kallas, A.1
Talpsep, T.2
-
33
-
-
33845756779
-
Impact of different inhibitor reactivities with commercial factor VIII concentrates on thrombin generation
-
Salvagno GL, Astermark J, Ekman M et.al. Impact of different inhibitor reactivities with commercial factor VIII concentrates on thrombin generation. Haemophilia 2007; 13: 51-6.
-
(2007)
, vol.13
, pp. 51-56
-
-
Salvagno, G.L.1
Astermark, J.2
Ekman, M.3
-
34
-
-
0141921426
-
Impact of inhibitor epitope profile on the neutralizing effect against plasma-derived and recombinant factor VIII concentrates in vitro
-
Astermark J, Voorberg J, Lenk H et.al. Impact of inhibitor epitope profile on the neutralizing effect against plasma-derived and recombinant factor VIII concentrates in vitro. Haemophilia 2003; 9: 567-72.
-
(2003)
, vol.9
, pp. 567-572
-
-
Astermark, J.1
Voorberg, J.2
Lenk, H.3
-
35
-
-
0030056318
-
Immune tolerance for the treatment of factor VIII inhibitors-twenty years''Bonn protocol'
-
Brackmann HH, Oldenburg J, Schwaab R. Immune tolerance for the treatment of factor VIII inhibitors-twenty years 'Bonn protocol'. Vox Sang 1996; 70 (Suppl. 1): 30-5.
-
(1996)
, vol.70
, pp. 30-35
-
-
Brackmann, H.H.1
Oldenburg, J.2
Schwaab, R.3
-
36
-
-
37749013518
-
Role of von Willebrand factor in immune tolerance induction
-
Abstract presented at the American Society of Hematology meeting in San Diego, CA, December
-
Heisel Kurth M, Christie B, Hanneman V et al. Role of von Willebrand factor in immune tolerance induction. Abstract presented at the American Society of Hematology meeting in San Diego, CA, December, 2004.
-
(2004)
-
-
Heisel Kurth, M.1
Christie, B.2
Hanneman, V.3
-
37
-
-
3943048700
-
Treatment of von Willebrand's Disease
-
Mannucci PM. Treatment of von Willebrand's Disease. N Engl J Med 2004; 351: 683-94.
-
(2004)
, vol.351
, pp. 683-694
-
-
Mannucci, P.M.1
-
38
-
-
0037443406
-
Von Willebrand disease type 1: A diagnosis in search of a disease
-
Sadler JE. Von Willebrand disease type 1: a diagnosis in search of a disease. Blood 2003; 101: 2089-93.
-
(2003)
, vol.101
, pp. 2089-2093
-
-
Sadler, J.E.1
-
39
-
-
33644977050
-
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: Results from a multicenter European study (MCMDM-1 VWD)
-
Tosetto A, Rodeghiero F, Castaman G et.al. A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: Results from a multicenter European study (MCMDM-1 VWD). J Thromb Haemost 2006; 4: 766-73.
-
(2006)
, vol.4
, pp. 766-773
-
-
Tosetto, A.1
Rodeghiero, F.2
Castaman, G.3
-
40
-
-
0034537373
-
Ristocetin cofactor and collagen binding activities normalized to antigen levels for a rapid diagnosis of type 2 von Willebrand disease-single center comparison of four different assays
-
Federici AB, Canciani MT, Forza I, Cozzi G. Ristocetin cofactor and collagen binding activities normalized to antigen levels for a rapid diagnosis of type 2 von Willebrand disease-single center comparison of four different assays. Thromb Haemost 2000; 84: 1127-8.
-
(2000)
, vol.84
, pp. 1127-1128
-
-
Federici, A.B.1
Canciani, M.T.2
Forza, I.3
Cozzi, G.4
-
41
-
-
33747161013
-
von Willebrand factor collagen binding assay in von Willebrand disease type 2A, 2B, and 2M
-
Baronciani L, Federici AB, Cozzi G, Canciani MT, Mannucci PM. von Willebrand factor collagen binding assay in von Willebrand disease type 2A, 2B, and 2M. J Thromb Haemost 2006; 4: 2088-90.
-
(2006)
, vol.4
, pp. 2088-2090
-
-
Baronciani, L.1
Federici, A.B.2
Cozzi, G.3
Canciani, M.T.4
Mannucci, P.M.5
-
42
-
-
19944376470
-
The evolving classification of von Willebrand disease
-
Schneppenheim R. The evolving classification of von Willebrand disease. Blood Coagul Fibrinolysis 2005; 16 (Suppl. 1): S3-10.
-
(2005)
, vol.16
-
-
Schneppenheim, R.1
-
43
-
-
37749019917
-
Secondary long-term prophylaxis in von Willebrand disease: An Italian cohort study
-
Federici AB, Gianniello F, Mannucci PM. Secondary long-term prophylaxis in von Willebrand disease: An Italian cohort study. Haematol Rep 2005; 1: 15-20.
-
(2005)
, vol.1
, pp. 15-20
-
-
Federici, A.B.1
Gianniello, F.2
Mannucci, P.M.3
-
44
-
-
19944364505
-
Long-term prophylaxis in von Willebrand disease
-
Berntorp E, Petrini P. Long-term prophylaxis in von Willebrand disease. Blood Coagul Fibrinolysis 2005; 16 (Suppl. 1): S23-6.
-
(2005)
, vol.16
-
-
Berntorp, E.1
Petrini, P.2
|