-
1
-
-
0036372012
-
Functional property of von Willebrand factor under flowing blood
-
Sugimoto M, Miyata S. Functional property of von Willebrand factor under flowing blood. Int J Hematol 2002; 75: 19-24.
-
(2002)
Int J Hematol
, vol.75
, pp. 19-24
-
-
Sugimoto, M.1
Miyata, S.2
-
2
-
-
3943048700
-
Treatment of von Willebrand's disease
-
Mannucci PM. Treatment of von Willebrand's disease. New Engl J Med 2004; 351: 683-694.
-
(2004)
New Engl J Med
, vol.351
, pp. 683-694
-
-
Mannucci, P.M.1
-
4
-
-
33646160453
-
Von Willebrand's disease: Clinical management
-
Federici AB, Castaman G, Thompson A, et al. Von Willebrand's disease: clinical management. Haemophilia 2006; 12 (Suppl 3): 152-158.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 3
, pp. 152-158
-
-
Federici, A.B.1
Castaman, G.2
Thompson, A.3
-
6
-
-
83055187115
-
von Willebrand disease (VWD): Evidence- based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA)
-
Nichols WL, Hultin MB, James AH, et al. von Willebrand disease (VWD): evidence- based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). Haemophilia 2008; 14: 171-232.
-
(2008)
Haemophilia
, vol.14
, pp. 171-232
-
-
Nichols, W.L.1
Hultin, M.B.2
James, A.H.3
-
7
-
-
33646158996
-
Characterisation of a novel high-purity, double virus inactivated von Willebrand Factor and Factor VIII concentrate (Wilate)
-
Stadler M, Gruber G, Kannicht C, et al. Characterisation of a novel high-purity, double virus inactivated von Willebrand Factor and Factor VIII concentrate (Wilate). Biologicals 2006; 34: 281-288.
-
(2006)
Biologicals
, vol.34
, pp. 281-288
-
-
Stadler, M.1
Gruber, G.2
Kannicht, C.3
-
8
-
-
32344449434
-
Evaluation of a rapid automated assay for analysis of von Willebrand ristocetin cofactor activity
-
Strandberg K, Lethagen S, Andersson K, et al. Evaluation of a rapid automated assay for analysis of von Willebrand ristocetin cofactor activity. Clin Appl Thromb Hemost 2006; 12: 61-67.
-
(2006)
Clin Appl Thromb Hemost
, vol.12
, pp. 61-67
-
-
Strandberg, K.1
Lethagen, S.2
Andersson, K.3
-
9
-
-
78649360891
-
Improved performance characteristics of the von Willebrand factor ristocetin cofactor activity assay using a novel automated assay protocol
-
Hillarp A, Stadler M, Haderer C, et al. Improved performance characteristics of the von Willebrand factor ristocetin cofactor activity assay using a novel automated assay protocol. J Thromb Haemost 2010; 8: 2216-2223.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 2216-2223
-
-
Hillarp, A.1
Stadler, M.2
Haderer, C.3
-
10
-
-
0036017368
-
Coagulation and chromogenic assays of factor VIII activity: General aspects, standardization, and recommendations
-
Barrowcliffe TW, Raut S, Sands D, et al. Coagulation and chromogenic assays of factor VIII activity: general aspects, standardization, and recommendations. Semin Thromb Hemost 2002; 28: 247-256.
-
(2002)
Semin Thromb Hemost
, vol.28
, pp. 247-256
-
-
Barrowcliffe, T.W.1
Raut, S.2
Sands, D.3
-
11
-
-
0035018552
-
Potency estimation of recombinant factor VIII: Effect of assay method and standard
-
Hubbard AR, Bevan SA, Weller LJ. Potency estimation of recombinant factor VIII: effect of assay method and standard. Br J Haematol 2001; 113: 533-536.
-
(2001)
Br J Haematol
, vol.113
, pp. 533-536
-
-
Hubbard, A.R.1
Bevan, S.A.2
Weller, L.J.3
-
12
-
-
0025236609
-
Luminographic detection of von Willebrand factor multimers in agarose gels and on nitrocellulose membranes
-
Budde U, Schneppenheim R, Plendl H, et al. Luminographic detection of von Willebrand factor multimers in agarose gels and on nitrocellulose membranes. Thromb Haemost 1990; 63: 312-315.
-
(1990)
Thromb Haemost
, vol.63
, pp. 312-315
-
-
Budde, U.1
Schneppenheim, R.2
Plendl, H.3
-
13
-
-
0031797825
-
Pharmacokinetics, efficacy and safety of Humate-P in von Willebrand disease
-
Dobrkovska A, Krzensk U, Chediak JR. Pharmacokinetics, efficacy and safety of Humate-P in von Willebrand disease. Haemophilia 1998; 4 (Suppl 3): 33-39.
-
(1998)
Haemophilia
, vol.4
, Issue.SUPPL. 3
, pp. 33-39
-
-
Dobrkovska, A.1
Krzensk, U.2
Chediak, J.R.3
-
14
-
-
34250691461
-
von Willebrand factor/factor VIII concentrate (Haemate P) dosing based on pharmacokinetics: A prospective multicenter trial in elective surgery
-
Lethagen S, Kyrle PA, Castaman G, et al. von Willebrand factor/factor VIII concentrate (Haemate P) dosing based on pharmacokinetics: a prospective multicenter trial in elective surgery. J Thromb Haemost 2007; 5: 1420-1430.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 1420-1430
-
-
Lethagen, S.1
Kyrle, P.A.2
Castaman, G.3
-
15
-
-
63049123172
-
Treatment and prevention of acute bleedings in von Willebrand disease - efficacy and safety of Wilate, a new generation von Willebrand factor/factor VIII concentrate
-
European Wilate Study Group
-
Berntorp E, Windyga A, European Wilate Study Group. Treatment and prevention of acute bleedings in von Willebrand disease - efficacy and safety of Wilate, a new generation von Willebrand factor/factor VIII concentrate. Haemophilia 2009; 15: 122-130.
-
(2009)
Haemophilia
, vol.15
, pp. 122-130
-
-
Berntorp, E.1
Windyga, A.2
-
16
-
-
71549152209
-
Haemate P/Humate-P: A Systematic review
-
Berntorp E. Haemate P/Humate-P: a Systematic review. Thromb Res 2009; 124 (Suppl 1): S11-14.
-
(2009)
Thromb Res
, vol.124
, Issue.SUPPL. 1
-
-
Berntorp, E.1
-
17
-
-
51349128727
-
Haemate P/Humate-P for the treatment of von Willebrand disease: Considerations for use and clinical experience
-
Auerswald G, Kreuz W. Haemate P/Humate-P for the treatment of von Willebrand disease: considerations for use and clinical experience. Haemophilia 2008; 14 (Suppl 5): 39-46.
-
(2008)
Haemophilia
, vol.14
, Issue.SUPPL. 5
, pp. 39-46
-
-
Auerswald, G.1
Kreuz, W.2
-
18
-
-
34250626034
-
Comparison of the pharmacokinetics of two von Willebrand factor concentrates [Biostate and AHF(High Purity)] in people with von Willebrand disorder-A randomized cross-over, multi-centre study
-
Favaloro EJ, Lloyd J, Rowell J, et al. Comparison of the pharmacokinetics of two von Willebrand factor concentrates [Biostate and AHF(High Purity)] in people with von Willebrand disorder-A randomized cross-over, multi-centre study. Thromb Haemost 2007; 97: 922-930.
-
(2007)
Thromb Haemost
, vol.97
, pp. 922-930
-
-
Favaloro, E.J.1
Lloyd, J.2
Rowell, J.3
-
19
-
-
79961049588
-
Does the von Willebrand factor (VWF) triplet structure affect VWF function?
-
Fuchs B, Solecka B, Kroening M, et al. Does the von Willebrand factor (VWF) triplet structure affect VWF function? Haemophilia 2010; 16 (Suppl 4): 1-158.
-
(2010)
Haemophilia
, vol.16
, Issue.SUPPL. 4
, pp. 1-158
-
-
Fuchs, B.1
Solecka, B.2
Kroening, M.3
-
20
-
-
0037079717
-
Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: A prospective, multicenter study
-
Mannucci PM, Chediak J, Hanna W, et al. Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: a prospective, multicenter study. Blood 2002; 99: 450-456.
-
(2002)
Blood
, vol.99
, pp. 450-456
-
-
Mannucci, P.M.1
Chediak, J.2
Hanna, W.3
-
21
-
-
0028814316
-
Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis
-
Koster T, Blann AD, Briet E, et al. Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis. Lancet 1995; 345: 152-155.
-
(1995)
Lancet
, vol.345
, pp. 152-155
-
-
Koster, T.1
Blann, A.D.2
Briet, E.3
-
22
-
-
0033983988
-
High plasma concentration of factor VIIIc is a major risk factor for venous thromboembolism
-
Kraaijenhagen RA, in't Anker PS, Koopman MM, et al. High plasma concentration of factor VIIIc is a major risk factor for venous thromboembolism. Thromb Haemost 2000; 83: 5-9.
-
(2000)
Thromb Haemost
, vol.83
, pp. 5-9
-
-
Kraaijenhagen, R.A.1
Anker, P.S.2
Koopman, M.M.3
-
23
-
-
0036713595
-
Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease
-
Makris M, Colvin B, Gupta V, et al. Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease. Thromb Haemost 2002; 88: 387-388.
-
(2002)
Thromb Haemost
, vol.88
, pp. 387-388
-
-
Makris, M.1
Colvin, B.2
Gupta, V.3
-
24
-
-
79958088726
-
Efficacy and safety of a new generation von Willebrand factor/factor VIII concentrate (Wilate) in the management of perioperative haemostasis in von Willebrand disease patients undergoing surgery
-
Windyga J, von Depka-Prondzinski M. Efficacy and safety of a new generation von Willebrand factor/factor VIII concentrate (Wilate) in the management of perioperative haemostasis in von Willebrand disease patients undergoing surgery. Thromb Haemost 2011; 105: 1072-1079.
-
(2011)
Thromb Haemost
, vol.105
, pp. 1072-1079
-
-
Windyga, J.1
von Depka-Prondzinski, M.2
|