-
1
-
-
0025280666
-
Glycoprotein Ib, von Willebrand factor, and glycoprotein IIb: IIIa are all involved in platelet adhesion to fibrin in flowing whole blood
-
Hantgan RR, Hindriks G, Taylor RG, Sixma JJ, de Groot PG. Glycoprotein Ib, von Willebrand factor, and glycoprotein IIb: IIIa are all involved in platelet adhesion to fibrin in flowing whole blood. Blood. 1990;76(2):345-353.
-
(1990)
Blood
, vol.76
, Issue.2
, pp. 345-353
-
-
Hantgan, R.R.1
Hindriks, G.2
Taylor, R.G.3
Sixma, J.J.4
De Groot, P.G.5
-
2
-
-
34249883835
-
Treatment of urgent bleeding in von Willebrand disease
-
Gill JC. Treatment of urgent bleeding in von Willebrand disease. Thromb Res. 2007;120(Suppl 1):S21-S25.
-
(2007)
Thromb Res
, vol.120
, pp. S21-S25
-
-
Gill, J.C.1
-
3
-
-
38649115965
-
Assembly of Weibel-Palade body-like tubules from N-terminal domains of von Willebrand factor
-
Huang RH, Wang Y, Roth R, et al. Assembly of Weibel-Palade body-like tubules from N-terminal domains of von Willebrand factor. Proc Natl Acad Sci USA. 2008;105(2):482-487.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.2
, pp. 482-487
-
-
Huang, R.H.1
Wang, Y.2
Roth, R.3
-
4
-
-
0021844825
-
Human von Willebrand factor (VWF): Isolation of complementary DNA (cDNA) clones and chromosomal localization
-
Ginsburg D, Handin RI, Bonthron DT, et al. Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization. Science. 1985;228(4706):1401-1406.
-
(1985)
Science
, vol.228
, Issue.4706
, pp. 1401-1406
-
-
Ginsburg, D.1
Handin, R.I.2
Bonthron, D.T.3
-
5
-
-
0024331438
-
Structure of the gene for human von Willebrand factor
-
Mancuso DJ, Tuley EA, Westfield LA, et al. Structure of the gene for human von Willebrand factor. J Biol Chem. 1989;264(33):19514-19527.
-
(1989)
J Biol Chem.
, vol.264
, Issue.33
, pp. 19514-19527
-
-
Mancuso, D.J.1
Tuley, E.A.2
Westfield, L.A.3
-
6
-
-
0023164845
-
Epidemiological investigation of the prevalence of von Willebrand's disease
-
Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of the prevalence of von Willebrand's disease. Blood. 1987;69(2):454-459.
-
(1987)
Blood
, vol.69
, Issue.2
, pp. 454-459
-
-
Rodeghiero, F.1
Castaman, G.2
Dini, E.3
-
7
-
-
33748802581
-
Update on the pathophysiology and classification of von Willebrand disease: A report of the Subcommittee on von Willebrand Factor
-
Sadler JE, Budde U, Eikenboom JC, et al; Working Party on von Willebrand Disease Classification. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. J Thromb Haemost. 2006;4(10):2103-2114.
-
(2006)
J Thromb Haemost.
, vol.4
, Issue.10
, pp. 2103-2114
-
-
Working Party on von Willebrand Disease Classification1
Sadler, J.E.2
Budde, U.3
Eikenboom, J.C.4
-
8
-
-
12144289138
-
Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: Results of a multicenter European study
-
Federici AB, Mazurier C, Berntorp E, et al. Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study. Blood. 2004;103(6):2032-2038.
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2032-2038
-
-
Federici, A.B.1
Mazurier, C.2
Berntorp, E.3
-
9
-
-
3943048700
-
Treatment of von Willebrand's disease
-
Mannucci PM. Treatment of von Willebrand's Disease. N Engl J Med. 2004;351(7):683-694.
-
(2004)
N Engl J Med.
, vol.351
, Issue.7
, pp. 683-694
-
-
Mannucci, P.M.1
-
10
-
-
28444472737
-
Pharmacokinetic studies on Wilfactin, a von Willebrand factor concentrate with a low factor VIII content treated with three virus-inactivation/removal methods
-
Goudemand J, Scharrer I, Berntorp E, et al. Pharmacokinetic studies on Wilfactin, a von Willebrand factor concentrate with a low factor VIII content treated with three virus-inactivation/removal methods. J Thromb Haemost. 2005;3(10):2219-2227.
-
(2005)
J Thromb Haemost.
, vol.3
, Issue.10
, pp. 2219-2227
-
-
Goudemand, J.1
Scharrer, I.2
Berntorp, E.3
-
11
-
-
34250169072
-
Treatment of severe von Willebrand disease with a high-purity von Willebrand factor concentrate (Wilfactin): A prospective study of 50 patients
-
Borel-Derlon A, Federici AB, Roussel-Robert V, et al. Treatment of severe von Willebrand disease with a high-purity von Willebrand factor concentrate (Wilfactin): a prospective study of 50 patients. J Thromb Haemost. 2007;5(6):1115-1124.
-
(2007)
J Thromb Haemost.
, vol.5
, Issue.6
, pp. 1115-1124
-
-
Borel-Derlon, A.1
Federici, A.B.2
Roussel-Robert, V.3
-
12
-
-
34250626034
-
Comparison of the pharmacokinetics of two von Willebrand factor concentrates [Biostate and AHF (High Purity)] in people with von Willebrand disorder. A randomised 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 randomised cross-over, multi-centre study. Thromb Haemost. 2007;97(6):922-930.
-
(2007)
Thromb Haemost.
, vol.97
, Issue.6
, pp. 922-930
-
-
Favaloro, E.J.1
Lloyd, J.2
Rowell, J.3
-
13
-
-
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, Haertel S, Mannucci PM; HAEMATE P Surgical Study Group. von Willebrand factor/factor VIII concentrate (Haemate P) dosing based on pharmacokinetics: a prospective multicenter trial in elective surgery. J Thromb Haemost. 2007;5(7):1420-1430.
-
(2007)
J Thromb Haemost.
, vol.5
, Issue.7
, pp. 1420-1430
-
-
Lethagen, S.1
Kyrle, P.A.2
Castaman, G.3
Haertel, S.4
Mannucci, P.M.5
-
14
-
-
84877700550
-
Evidence for the transmission of parvovirus B19 in patients with bleeding disorders treated with plasma-derived factor concentrates in the era of nucleic acid test screening
-
Soucie JM, De Staercke C, Monahan PE, et al; US Hemophilia Treatment Center Network. Evidence for the transmission of parvovirus B19 in patients with bleeding disorders treated with plasma-derived factor concentrates in the era of nucleic acid test screening. Transfusion. 2013;53(6):1217-1225.
-
(2013)
Transfusion
, vol.53
, Issue.6
, pp. 1217-1225
-
-
US Hemophilia Treatment Center Network1
Soucie, J.M.2
De Staercke, C.3
Monahan, P.E.4
-
15
-
-
84884924159
-
Pathogen safety of long-term treatments for bleeding disorders: Still relevant to current practice
-
Di Minno G, Canaro M, Ironside JW, et al. Pathogen safety of long-term treatments for bleeding disorders: still relevant to current practice. Haematologica. 2013;98(10):1495-1498.
-
(2013)
Haematologica
, vol.98
, Issue.10
, pp. 1495-1498
-
-
Di Minno, G.1
Canaro, M.2
Ironside, J.W.3
-
16
-
-
0026650784
-
Comparison of four virusinactivated plasma concentrates for treatment of severe von Willebrand disease: A cross-over randomized trial
-
Mannucci PM, Tenconi PM, Castaman G, Rodeghiero F. Comparison of four virusinactivated plasma concentrates for treatment of severe von Willebrand disease: a cross-over randomized trial. Blood. 1992;79(12):3130-3137.
-
(1992)
Blood
, vol.79
, Issue.12
, pp. 3130-3137
-
-
Mannucci, P.M.1
Tenconi, P.M.2
Castaman, G.3
Rodeghiero, F.4
-
17
-
-
0028314508
-
Proteolysis of von Willebrand factor in therapeutic plasma concentrates
-
Mannuccio PM, Lattuada A, Ruggeri ZM. Proteolysis of von Willebrand factor in therapeutic plasma concentrates. Blood. 1994;83(10):3018-3027.
-
(1994)
Blood
, vol.83
, Issue.10
, pp. 3018-3027
-
-
Mannuccio, P.M.1
Lattuada, A.2
Ruggeri, Z.M.3
-
18
-
-
33749011946
-
Comparative analysis and classification of von Willebrand factor/factor VIII concentrates: Impact on treatment of patients with von Willebrand disease
-
Budde U, Metzner HJ, Müller HG. Comparative analysis and classification of von Willebrand factor/factor VIII concentrates: impact on treatment of patients with von Willebrand disease. Semin Thromb Hemost. 2006;32(6):626-635.
-
(2006)
Semin Thromb Hemost
, vol.32
, Issue.6
, pp. 626-635
-
-
Budde, U.1
Metzner, H.J.2
Müller, H.G.3
-
19
-
-
2342591992
-
A comparative in vitro evaluation of six von Willebrand factor concentrates
-
Lethagen S, Carlson M, Hillarp A. A comparative in vitro evaluation of six von Willebrand factor concentrates. Haemophilia. 2004;10(3):243-249.
-
(2004)
Haemophilia
, vol.10
, Issue.3
, pp. 243-249
-
-
Lethagen, S.1
Carlson, M.2
Hillarp, A.3
-
20
-
-
43949117736
-
Plasmaderived biological medicines used to promote haemostasis
-
Ofosu FA, Freedman J, Semple JW. Plasmaderived biological medicines used to promote haemostasis. Thromb Haemost. 2008;99(5):851-862.
-
(2008)
Thromb Haemost
, vol.99
, Issue.5
, pp. 851-862
-
-
Ofosu, F.A.1
Freedman, J.2
Semple, J.W.3
-
21
-
-
0032705572
-
Recombinant von Willebrand factor: Potential therapeutic use
-
Fischer BE. Recombinant von Willebrand factor: potential therapeutic use. J Thromb Thrombolysis. 1999;8(3):197-205.
-
(1999)
J Thromb Thrombolysis
, vol.8
, Issue.3
, pp. 197-205
-
-
Fischer, B.E.1
-
22
-
-
77954877699
-
Structure and function of a recombinant von Willebrand factor drug candidate
-
Turecek PL, Schrenk G, Rottensteiner H, et al. Structure and function of a recombinant von Willebrand factor drug candidate. Semin Thromb Hemost. 2010;36(5):510-521.
-
(2010)
Semin Thromb Hemost
, vol.36
, Issue.5
, pp. 510-521
-
-
Turecek, P.L.1
Schrenk, G.2
Rottensteiner, H.3
-
23
-
-
84885638015
-
Pharmacokinetics and safety of a novel recombinant human von Willebrand factor manufactured with a plasma-free method: A prospective clinical trial
-
Mannucci PM, Kempton C, Millar C, et al; rVWF Ad Hoc Study Group. Pharmacokinetics and safety of a novel recombinant human von Willebrand factor manufactured with a plasma-free method: a prospective clinical trial. Blood. 2013;122(5):648-657.
-
(2013)
Blood
, vol.122
, Issue.5
, pp. 648-657
-
-
Mannucci, P.M.1
Kempton, C.2
Millar, C.3
-
24
-
-
0036166457
-
Efficacy and safety of the factor VIII/von Willebrand factor concentrate, haemate-P/humate-P: Ristocetin cofactor unit dosing in patients with von Willebrand disease
-
Lillicrap D, Poon MC, Walker I, Xie F, Schwartz BA; Association of Hemophilia Clinic Directors of Canada. Efficacy and safety of the factor VIII/von Willebrand factor concentrate, haemate-P/humate-P: ristocetin cofactor unit dosing in patients with von Willebrand disease. Thromb Haemost. 2002;87(2):224-230.
-
(2002)
Thromb Haemost
, vol.87
, Issue.2
, pp. 224-230
-
-
Association of Hemophilia Clinic Directors of Canada1
Lillicrap, D.2
Poon, M.C.3
Walker, I.4
Xie, F.5
Schwartz, B.A.6
-
25
-
-
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; Alphanate Study Group. Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: a prospective, multicenter study. Blood. 2002;99(2):450-456.
-
(2002)
Blood
, vol.99
, Issue.2
, pp. 450-456
-
-
Mannucci, P.M.1
Chediak, J.2
Hanna, W.3
-
26
-
-
0003042160
-
Laboratory tests for factor VIII inhibitors, their variation, significance and interpretation
-
Kasper CK. Laboratory tests for factor VIII inhibitors, their variation, significance and interpretation. Blood Coagul Fibrinolysis. 1991;2(Suppl 1):7-10.
-
(1991)
Blood Coagul Fibrinolysis
, vol.2
, pp. 7-10
-
-
Kasper, C.K.1
-
27
-
-
84873583409
-
Distinct characteristics of antibody responses against factor VIII in healthy individuals and in different cohorts of hemophilia A patients
-
Whelan SF, Hofbauer CJ, Horling FM, et al. Distinct characteristics of antibody responses against factor VIII in healthy individuals and in different cohorts of hemophilia A patients. Blood. 2013;121(6):1039-1048.
-
(2013)
Blood
, vol.121
, Issue.6
, pp. 1039-1048
-
-
Whelan, S.F.1
Hofbauer, C.J.2
Horling, F.M.3
-
28
-
-
75549090170
-
Development of a plasma- and albuminfree recombinant von Willebrand factor
-
Turecek PL, Mitterer A, Matthiessen HP, et al. Development of a plasma- and albuminfree recombinant von Willebrand factor. Hamostaseologie. 2009;29(Suppl 1):S32-S38.
-
(2009)
Hamostaseologie
, vol.29
, pp. S32-S38
-
-
Turecek, P.L.1
Mitterer, A.2
Matthiessen, H.P.3
-
29
-
-
32344449434
-
Evaluation of a rapid automated assay for analysis of von Willebrand ristocetin cofactor activity
-
Strandberg K, Lethagen S, Andersson K, Carlson M, Hillarp A. Evaluation of a rapid automated assay for analysis of von Willebrand ristocetin cofactor activity. Clin Appl Thromb Hemost. 2006;12(1):61-67.
-
(2006)
Clin Appl Thromb Hemost
, vol.12
, Issue.1
, pp. 61-67
-
-
Strandberg, K.1
Lethagen, S.2
Andersson, K.3
Carlson, M.4
Hillarp, A.5
-
30
-
-
62349135194
-
Von Willebrand factor/factor VIII concentrates in the treatment of von Willebrand disease
-
Batlle J, López-Fernández MF, Fraga EL, Trillo AR, Pérez-Rodríguez MA. Von Willebrand factor/factor VIII concentrates in the treatment of von Willebrand disease. Blood Coagul Fibrinolysis. 2009;20(2):89-100.
-
(2009)
Blood Coagul Fibrinolysis
, vol.20
, Issue.2
, pp. 89-100
-
-
Batlle, J.1
López-Fernández, M.F.2
Fraga, E.L.3
Trillo, A.R.4
Pérez-Rodríguez, M.A.5
-
31
-
-
79961073761
-
The pharmacokinetic diversity of two von Willebrand factor (VWF)/factor VIII (FVIII) concentrates in subjects with congenital von Willebrand disease. Results from a prospective, randomised crossover study
-
Kessler CM, Friedman K, Schwartz BA, Gill JC, Powell JS; Wilate PK Study Investigators. The pharmacokinetic diversity of two von Willebrand factor (VWF)/factor VIII (FVIII) concentrates in subjects with congenital von Willebrand disease. Results from a prospective, randomised crossover study. Thromb Haemost. 2011;106(2):279-288.
-
(2011)
Thromb Haemost
, vol.106
, Issue.2
, pp. 279-288
-
-
Wilate PK Study Investigators1
Kessler, C.M.2
Friedman, K.3
Schwartz, B.A.4
Gill, J.C.5
Powell, J.S.6
-
32
-
-
19944386220
-
Management of von Willebrand disease with factor VIII/von Willebrand factor concentrates: Results from current studies and surveys
-
Federici AB. Management of von Willebrand disease with factor VIII/von Willebrand factor concentrates: results from current studies and surveys. Blood Coagul Fibrinolysis. 2005;16(Suppl 1):S17-S21.
-
(2005)
Blood Coagul Fibrinolysis
, vol.16
, pp. S17-S21
-
-
Federici, A.B.1
-
33
-
-
0031686041
-
Biochemistry and genetics of von Willebrand factor
-
Sadler JE. Biochemistry and genetics of von Willebrand factor. Annu Rev Biochem. 1998;67:395-424.
-
(1998)
Annu Rev Biochem
, vol.67
, pp. 395-424
-
-
Sadler, J.E.1
-
34
-
-
51349164922
-
Function of von Willebrand factor in haemostasis and thrombosis
-
Reininger AJ. Function of von Willebrand factor in haemostasis and thrombosis. Haemophilia. 2008;14(Suppl 5):11-26.
-
(2008)
Haemophilia
, vol.14
, pp. 11-26
-
-
Reininger, A.J.1
-
35
-
-
84900496261
-
High shear dependent von Willebrand factor self-assembly fostered by platelet interaction and controlled by ADAMTS13
-
Kragh T, Napoleone M, Fallah MA, Gritsch H, Schneider MF, Reininger AJ. High shear dependent von Willebrand factor self-assembly fostered by platelet interaction and controlled by ADAMTS13. Thromb Res. 2014;133(6):1079-1087.
-
(2014)
Thromb Res.
, vol.133
, Issue.6
, pp. 1079-1087
-
-
Kragh, T.1
Napoleone, M.2
Fallah, M.A.3
Gritsch, H.4
Schneider, M.F.5
Reininger, A.J.6
-
36
-
-
84859169124
-
Different bleeding risk in type 2A and 2M von Willebrand disease: A 2-year prospective study in 107 patients
-
Castaman G, Federici AB, Tosetto A, et al. Different bleeding risk in type 2A and 2M von Willebrand disease: a 2-year prospective study in 107 patients. J Thromb Haemost. 2012;10(4):632-638.
-
(2012)
J Thromb Haemost.
, vol.10
, Issue.4
, pp. 632-638
-
-
Castaman, G.1
Federici, A.B.2
Tosetto, A.3
-
37
-
-
84939553295
-
The function of ultra-large von Willebrand factor multimers in high shear flow controlled by ADAMTS13
-
Reininger AJ. The function of ultra-large von Willebrand factor multimers in high shear flow controlled by ADAMTS13. Hamostaseologie. 2015;35(3):225-233.
-
(2015)
Hamostaseologie.
, vol.35
, Issue.3
, pp. 225-233
-
-
Reininger, A.J.1
-
38
-
-
84886395616
-
Alloantibodies in von Willebrand disease
-
James PD, Lillicrap D, Mannucci PM. Alloantibodies in von Willebrand disease. Blood. 2013;122(5):636-640.
-
(2013)
Blood
, vol.122
, Issue.5
, pp. 636-640
-
-
James, P.D.1
Lillicrap, D.2
Mannucci, P.M.3
|