-
2
-
-
0033858187
-
Impact, diagnosis and treatment of von Willebrand disease
-
Sadler JE, Mannucci PM, Berntorp E, et al. Impact, diagnosis and treatment of von Willebrand disease. Thromb Haemost. 2000; 84(2): 160-174. (Pubitemid 30601459)
-
(2000)
Thrombosis and Haemostasis
, vol.84
, Issue.2
, pp. 160-174
-
-
Sadler, J.E.1
Mannucci, P.M.2
Berntorp, E.3
Bochkov, N.4
Boulyjenkov, V.5
Ginsburg, D.6
Meyer, D.7
Peake, I.8
Rodeghiero, F.9
Srivastava, A.10
-
3
-
-
0017754787
-
Stabilization of factor VIII in plasma by the von Willebrand factor. Studies on posttransfusion and dissociated factor VIII and in patients with von Willebrand's disease
-
Weiss HJ, Sussman II, Hoyer LW. Stabilization of factor VIII in plasma by the von Willebrand factor. Studies on posttransfusion and dissociated factor VIII and in patients with von Willebrand's disease. J Clin Invest. 1977; 60(2): 390-404. (Pubitemid 8154146)
-
(1977)
Journal of Clinical Investigation
, vol.60
, Issue.2
, pp. 390-404
-
-
Weiss, H.J.1
Sussman, I.I.2
Hoyer, L.W.3
-
4
-
-
0025748557
-
The role of von Willebrand Factor multimers and propeptide cleavage in binding and stabilization of factor VIII
-
Wise RJ, Dorner AJ, Krane M, Pittman D.D., Kaufman RJ. The role of von Willebrand factor multimers and propeptide cleavage in binding and stabilization of factor VIII. J Biol Chem. 1991; 266(32): 21948-21955. (Pubitemid 121000273)
-
(1991)
Journal of Biological Chemistry
, vol.266
, Issue.32
, pp. 21948-21955
-
-
Wise, R.J.1
Dorner, A.J.2
Krane, M.3
Pittman, D.D.4
Kaufman, R.J.5
-
5
-
-
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
-
6
-
-
0032725346
-
Molecular genetics of von willebrand disease
-
Ginsburg D. Molecular genetics of von Willebrand disease. Thromb Haemost. 1999; 82(2): 585-591.
-
(1999)
Thromb Haemost.
, vol.82
, Issue.2
, pp. 585-591
-
-
Ginsburg, D.1
-
7
-
-
0037079717
-
Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: A prospective, multicenter study
-
DOI 10.1182/blood.V99.2.450
-
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. (Pubitemid 34533078)
-
(2002)
Blood
, vol.99
, Issue.2
, pp. 450-456
-
-
Mannucci, P.M.1
Chediak, J.2
Hanna, W.3
Byrnes, J.4
Ledford, M.5
Ewenstein, B.M.6
Retzios, A.D.7
Kapelan, B.A.8
Schwartz, R.S.9
Kessler, C.10
-
8
-
-
10744230522
-
Successful treatment of urgent bleeding in von Willebrand disease with factor VIII/VWF concentrate (Humate-P): Use of the ristocetin cofactor assay (VWF:RCo) to measure potency and to guide therapy
-
Gill JC, Ewenstein BM, Thompson A.R., Mueller-Velten G, Schwartz BA; Humate-P Study Group. Successful treatment of urgent bleeding in von Willebrand disease with factor VIII/VWF concentrate (Humate-P): use of the ristocetin cofactor assay (VWF:RCo) to measure potency and to guide therapy. Haemophilia. 2003; 9(6): 688-695. (Pubitemid 37540809)
-
(2003)
Haemophilia
, vol.9
, Issue.6
, pp. 688-695
-
-
Gill, J.C.1
Ewenstein, B.M.2
Thompson, A.R.3
Mueller-Velten, G.4
Schwartz, B.A.5
Abshire, T.6
Ambinder, R.7
Angiolillo, A.8
Arkel, Y.9
Beardsley, D.10
Benjamin, R.11
Binder, M.12
Charbel, F.13
Cooper, B.14
Cornell, N.15
Czapek, E.16
Eisenberg, P.17
Ewenstein, B.18
Garcia-Ortiz, S.19
Gastineau, D.20
Gill, J.21
Heggie, G.22
Heisel, M.23
Joist, H.24
Knupp, C.25
Lewis, B.26
Matthews, D.27
McKenna, P.28
Murukutla, S.29
Palascak, J.30
Penner, J.31
Powell, J.32
Ritter, H.33
Francisco, R.34
Shapiro, A.35
Simpson, T.36
Stanek, M.37
Thompson, A.R.38
Tongol, J.39
Waterbury, L.40
White, G.41
Young, R.42
more..
-
9
-
-
0036860649
-
Clinical efficacy of highly purified, doubly virus-inactivated factor VIII/von Willebrand factor concentrate (Fanhdi) in the treatment of von Willebrand disease: A retropective clinical study
-
Federici AB, Baudo F, Caracciolo C., et al. Clinical efficacy of highly purified, doubly virus-inactivated factor VIII/von Willebrand factor concentrate (Fanhdi) in the treatment of von Willebrand disease: a retrospective clinical study. Haemophilia. 2002; 8(6): 761-767. (Pubitemid 35446628)
-
(2002)
Haemophilia
, vol.8
, Issue.6
, pp. 761-767
-
-
Federici, A.B.1
Baudo, F.2
Caracciolo, C.3
Mancuso, G.4
Mazzuconi, M.G.5
Musso, R.6
Schinco, P.C.7
Targhetta, R.8
Mannuccio Mannucci, P.9
-
10
-
-
0032705572
-
Recombinant von Willebrand factor: Potential therapeutic use
-
DOI 10.1023/A:1008906103637
-
Fischer BE. Recombinant von Willebrand factor: potential therapeutic use. J Thromb Thrombolysis. 1999; 8(3): 197-205. (Pubitemid 29497773)
-
(1999)
Journal of Thrombosis and Thrombolysis
, vol.8
, Issue.3
, pp. 197-205
-
-
Fischer, B.E.1
-
11
-
-
75549090170
-
Development of a plasma- and albumin-free recombinant von willebrand factor
-
Turecek PL, Mitterer A, Matthiessen H.P., et al. Development of a plasma- and albumin-free recombinant von Willebrand factor. Hamostaseologie. 2009; 29(SUPPL. 1):S32-S38.
-
(2009)
Hamostaseologie.
, vol.29
, Issue.SUPPL. 1
-
-
Turecek, P.L.1
Mitterer, A.2
Matthiessen, H.P.3
-
13
-
-
28444472737
-
Pharmacokinetic studies on Wilfactin, a von Willebrand factor concentrate with a low factor VIII content treated with three virus-inactivation/removal methods
-
DOI 10.1111/j.1538-7836.2005.01435.x
-
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. (Pubitemid 41727200)
-
(2005)
Journal of Thrombosis and Haemostasis
, vol.3
, Issue.10
, pp. 2219-2227
-
-
Goudemand, J.1
Scharrer, I.2
Berntorp, E.3
Lee, C.A.4
Borel-Derlon, A.5
Stieltjes, N.6
Caron, C.7
Scherrmann, J.M.8
Bridey, F.9
Tellier, Z.10
Federici, A.B.11
Mannucci, P.M.12
-
14
-
-
34250626034
-
Comparison of the pharmacokinetics of two von Willebrand factor concentrates [Biostate and AHF (High Purity)] in people with von Willebrand disorder
-
DOI 10.1160/TH06-09-0495
-
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. (Pubitemid 46939204)
-
(2007)
Thrombosis and Haemostasis
, vol.97
, Issue.6
, pp. 922-930
-
-
Favaloro, E.J.1
Lloyd, J.2
Rowell, J.3
Baker, R.4
Rickard, K.5
Kershaw, G.6
Street, A.7
Scarff, K.8
Barrese, G.9
Maher, D.10
McLachlan, A.J.11
-
15
-
-
0001312511
-
Algorithm AS 183. An efficient and portable pseudo-random number generator
-
Wichmann BA, Hill ID. Algorithm AS 183. An efficient and portable pseudo-random number generator. J R Stat Soc Ser C Appl Stat. 1982; 31(2): 188-190.
-
(1982)
J R Stat Soc Ser C Appl Stat.
, vol.31
, Issue.2
, pp. 188-190
-
-
Wichmann, B.A.1
Hill, I.D.2
-
16
-
-
0002391815
-
The clinical evaluation of chemotherapeutic agents in cancer
-
MacLeod CM, ed. New York, NY: Columbia University Press
-
Karnofsky DA, Burchenal JH. The clinical evaluation of chemotherapeutic agents in cancer. In: MacLeod CM, ed. Evaluation of Chemotherapeutic Agents. New York, NY: Columbia University Press; 1949: 191-205.
-
(1949)
Evaluation of Chemotherapeutic Agents
, pp. 191-205
-
-
Karnofsky, D.A.1
Burchenal, J.H.2
-
17
-
-
84887936184
-
Establishment of an automated VWF: RCo assay for measuring plasma samples with low activity [abstract]
-
Varadi K, Rottensteiner H, Gruber E., et al. Establishment of an automated VWF: RCo assay for measuring plasma samples with low activity [abstract]. J Thromb Haemost. 2011; 9(suppl 2): 919.
-
(2011)
J Thromb Haemost.
, vol.9
, Issue.SUPPL. 2
, pp. 919
-
-
Varadi, K.1
Rottensteiner, H.2
Gruber, E.3
-
18
-
-
17144408687
-
FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay
-
DOI 10.1111/j.1365-2141.2005.05420.x
-
Kokame K, Nobe Y, Kokubo Y., Okayama A, Miyata T. FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay. Br J Haematol. 2005; 129(1): 93-100. (Pubitemid 40524057)
-
(2005)
British Journal of Haematology
, vol.129
, Issue.1
, pp. 93-100
-
-
Kokame, K.1
Nobe, Y.2
Kokubo, Y.3
Okayama, A.4
Miyata, T.5
-
19
-
-
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
, Issue.SUPPL. 1
, pp. 7-10
-
-
Kasper, C.K.1
-
20
-
-
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 F.M., 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
-
21
-
-
0029842964
-
Results of a screening for von Willebrand disease type 2N in patients with suspected haemophilia A or von Willebrand disease type 1
-
Schneppenheim R, Budde U, Krey S., et al. Results of a screening for von Willebrand disease type 2N in patients with suspected haemophilia A or von Willebrand disease type 1. Thromb Haemost. 1996; 76(4): 598-602. (Pubitemid 26372017)
-
(1996)
Thrombosis and Haemostasis
, vol.76
, Issue.4
, pp. 598-602
-
-
Schneppenheim, R.1
Budde, U.2
Krey, S.3
Drewke, E.4
Bergmann, F.5
Lechler, E.6
Oldenburg, J.7
Schwaab, R.8
-
22
-
-
0034898818
-
Recommended abbreviations for von Willebrand Factor and its activities
-
Mazurier C, Rodeghiero F; von Willebrand Factor Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Recommended abbreviations for von Willebrand Factor and its activities. Thromb Haemost. 2001; 86(2): 712. (Pubitemid 32743290)
-
(2001)
Thrombosis and Haemostasis
, vol.86
, Issue.2
, pp. 712
-
-
Mazurier, C.1
Rodeghiero, F.2
-
23
-
-
0035001737
-
A standard nomenclature for von Willebrand factor gene mutations and polymorphisms
-
Goodeve AC, Eikenboom JC, Ginsburg D, et al.; ISTH SSC Subcommittee on von Willebrand factor. A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factor. Thromb Haemost. 2001; 85(5): 929-931. (Pubitemid 32421830)
-
(2001)
Thrombosis and Haemostasis
, vol.85
, Issue.5
, pp. 929-931
-
-
Goodeve, A.C.1
Eikenboom, J.C.J.2
Ginsburg, D.3
Hilbert, L.4
Mazurier, C.5
Peake, I.R.6
Sadler, J.E.7
Rodeghiero, F.8
-
24
-
-
0035119995
-
Use of ristocetin cofactor activity in the management of von Willebrand disease
-
DOI 10.1046/j.1365-2516.2001.00096.x
-
Ewenstein BM. Use of ristocetin cofactor activity in the management of von Willebrand disease. Haemophilia. 2001; 7(SUPPL. 1): 10-15. (Pubitemid 32184435)
-
(2001)
Haemophilia
, vol.7
, Issue.SUPPL. 1
, pp. 10-15
-
-
Ewenstein, B.M.1
-
25
-
-
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
-
26
-
-
11144354028
-
Hemophilia therapy innovation: Development of an advanced category recombinant factor VIII by a plasma/albumin-free method. Proceedings of a special symposium at the XIXth congress of the international society on thrombosis and haemostasis, july 12-18, 2003, birmingham, UK
-
discussion 16-18
-
Ewenstein BM, Collins P, Tarantino M.D., et al. Hemophilia therapy innovation: development of an advanced category recombinant factor VIII by a plasma/albumin-free method. Proceedings of a Special Symposium at the XIXth Congress of the International Society on Thrombosis and Haemostasis, July 12-18, 2003, Birmingham, UK. Semin Hematol. 2004; 41(1 suppl 2): 1-16, discussion 16-18
-
(2004)
Semin Hematol.
, vol.41
, Issue.1 SUPPL. 2
, pp. 1-16
-
-
Ewenstein, B.M.1
Collins, P.2
Tarantino, M.D.3
-
27
-
-
38949166825
-
Clearance of von Willebrand factor
-
DOI 10.1160/TH07-10-0629
-
Denis CV, Christophe OD, Oortwijn B.D., Lenting PJ. Clearance of von Willebrand factor. Thromb Haemost. 2008; 99(2): 271-278. (Pubitemid 351230955)
-
(2008)
Thrombosis and Haemostasis
, vol.99
, Issue.2
, pp. 271-278
-
-
Denis, C.V.1
Christophe, O.D.2
Oortwijn, B.D.3
Lenting, P.J.4
-
28
-
-
69449088981
-
Models for prediction of factor VIII half-life in severe haemophiliacs: Distinct approaches for blood group O and non-O patients
-
Fischer K, Pendu R, van Schooten CJ, et al. Models for prediction of factor VIII half-life in severe haemophiliacs: distinct approaches for blood group O and non-O patients. PLoS ONE. 2009; 4(8):e6745.
-
(2009)
PLoS ONE
, vol.4
, Issue.8
-
-
Fischer, K.1
Pendu, R.2
Van Schooten, C.J.3
-
29
-
-
84871043342
-
Von Willebrand factor: The old, the new and the unknown
-
Lenting PJ, Casari C, Christophe O.D., Denis CV. von Willebrand factor: the old, the new and the unknown. J Thromb Haemost. 2012; 10(12): 2428-2437.
-
(2012)
J Thromb Haemost.
, vol.10
, Issue.12
, pp. 2428-2437
-
-
Lenting, P.J.1
Casari, C.2
Christophe, O.D.3
Denis, C.V.4
-
30
-
-
0031932313
-
Factor VIII and von Willebrand factor
-
Vlot AJ, Koppelman SJ, Bouma B.N., Sixma JJ. Factor VIII and von Willebrand factor. Thromb Haemost. 1998; 79(3): 456-465. (Pubitemid 28120774)
-
(1998)
Thrombosis and Haemostasis
, vol.79
, Issue.3
, pp. 456-465
-
-
Vlot, A.J.1
Koppelman, S.J.2
Bouma, B.N.3
Sixma, J.J.4
-
31
-
-
44949086574
-
Factor VIII accelerates proteolytic cleavage of von Willebrand factor by ADAMTS13
-
DOI 10.1073/pnas.0801735105
-
Cao W, Krishnaswamy S, Camire R.M., Lenting PJ, Zheng XL. Factor VIII accelerates proteolytic cleavage of von Willebrand factor by ADAMTS13. Proc Natl Acad Sci USA. 2008; 105(21): 7416-7421. (Pubitemid 351830032)
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.21
, pp. 7416-7421
-
-
Cao, W.1
Krishnaswamy, S.2
Camire, R.M.3
Lenting, P.J.4
Zheng, X.L.5
-
32
-
-
9544220778
-
Pharmacokinetics of von Willebrand factor and factor VIIIC in patients with severe von Willebrand disease (type 3 VWD): Estimation of the rate of factor VIIIC synthesis
-
Menache D, Aronson DL, Darr F, et al.; Cooperative Study Groups. Pharmacokinetics of von Willebrand factor and factor VIIIC in patients with severe von Willebrand disease (type 3 VWD): estimation of the rate of factor VIIIC synthesis. Br J Haematol. 1996; 94(4): 740-745. (Pubitemid 26308912)
-
(1996)
British Journal of Haematology
, vol.94
, Issue.4
, pp. 740-745
-
-
Menache, D.1
Aronson, D.L.2
Darr, F.3
Montgomery, R.R.4
Gill, J.C.5
Kessler, C.M.6
Lusher, J.M.7
Phatak, P.D.8
Shapiro, A.D.9
Thompson, A.R.10
White II, G.C.11
-
33
-
-
47249144803
-
Von willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura
-
Sadler JE. Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura. Blood. 2008; 112(1): 11-18.
-
(2008)
Blood
, vol.112
, Issue.1
, pp. 11-18
-
-
Sadler, J.E.1
-
34
-
-
67649458188
-
Species-dependent variability of ADAMTS13-mediated proteolysis of human recombinant von willebrand factor
-
Varadi K, Rottensteiner H, Vejda S., et al. Species-dependent variability of ADAMTS13-mediated proteolysis of human recombinant von Willebrand factor. J Thromb Haemost. 2009; 7(7): 1134-1142.
-
(2009)
J Thromb Haemost.
, vol.7
, Issue.7
, pp. 1134-1142
-
-
Varadi, K.1
Rottensteiner, H.2
Vejda, S.3
-
35
-
-
0031773567
-
Characterization of factor VIII/von Willebrand factor concentrates using a modified method of von Willebrand factor multimer analysis
-
DOI 10.1046/j.1365-2516.1998.0040s3025.x
-
Metzner HJ, Hermentin P, Cuesta-Linker T, Langner S., Müller HG, Friedebold J. Characterization of factor VIII/von Willebrand factor concentrates using a modified method of von Willebrand factor multimer analysis. Haemophilia. 1998; 4(SUPPL. 3): 25-32. (Pubitemid 28561093)
-
(1998)
Haemophilia
, vol.4
, Issue.SUPPL. 3
, pp. 25-32
-
-
Metzner, H.J.1
Hermentin, P.2
Cuesta-Linker, T.3
Langner, S.4
Muller, H.-G.5
Friedebold, J.6
-
36
-
-
77956514337
-
Factor VIII and platelets synergistically accelerate cleavage of von willebrand factor by ADAMTS13 under fluid shear stress
-
Skipwith CG, Cao W, Zheng XL. Factor VIII and platelets synergistically accelerate cleavage of von Willebrand factor by ADAMTS13 under fluid shear stress. J Biol Chem. 2010; 285(37): 28596-28603.
-
(2010)
J Biol Chem.
, vol.285
, Issue.37
, pp. 28596-28603
-
-
Skipwith, C.G.1
Cao, W.2
Zheng, X.L.3
-
37
-
-
84886395616
-
Alloantibodies in von willebrand disease
-
published online ahead of print January 7
-
James PD, Lillicrap D, Mannucci PM. Alloantibodies in von Willebrand disease [published online ahead of print January 7, 2013]. Blood.
-
(2013)
Blood
-
-
James, P.D.1
Lillicrap, D.2
Mannucci, P.M.3
-
38
-
-
0025008771
-
Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: Family studies that identify carriers of the condition and a compound heterozygous individual
-
Peake IR, Liddell MB, Moodie P, et al. Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individual. Blood. 1990; 75(3): 654-661. (Pubitemid 20069205)
-
(1990)
Blood
, vol.75
, Issue.3
, pp. 654-661
-
-
Peake, I.R.1
Liddell, M.B.2
Moodie, P.3
Standen, G.4
Mancuso, D.J.5
Tuley, E.A.6
Westfield, L.A.7
Sorace, J.M.8
Sadler, J.E.9
Verweij, C.L.10
Bloom, A.L.11
-
39
-
-
0027930458
-
Characterization of partial gene deletions in type III von Willebrand disease with alloantibody inhibitors
-
Mancuso DJ, Tuley EA, Castillo R, de Bosch N, Mannucci PM, Sadler JE. Characterization of partial gene deletions in type III von Willebrand disease with alloantibody inhibitors. Thromb Haemost. 1994; 72(2): 180-185. (Pubitemid 24251276)
-
(1994)
Thrombosis and Haemostasis
, vol.72
, Issue.2
, pp. 180-185
-
-
Mancuso, D.J.1
Tuley, E.A.2
Castillo, R.3
De Bosch, N.4
Mannucci, P.M.5
Sadler, J.E.6
-
40
-
-
0023237159
-
Gene deletions correlate with the development of alloantibodies in von Willebrand disease
-
Shelton-Inloes B.B., Chehab FF, Mannucci P.M., Federici AB, Sadler JE. Gene deletions correlate with the development of alloantibodies in von Willebrand disease. J Clin Invest. 1987; 79(5): 1459-1465. (Pubitemid 17099650)
-
(1987)
Journal of Clinical Investigation
, vol.79
, Issue.5
, pp. 1459-1465
-
-
Shelton-Inloes, B.B.1
Chehab, F.F.2
Mannucci, P.M.3
-
41
-
-
0035412405
-
Homozygous gene conversion in von willebrand factor gene as a cause of type 3 von willebrand disease and predisposition to inhibitor development
-
Surdhar GK, Enayat MS, Lawson S, Williams M.D., Hill FG. Homozygous gene conversion in von Willebrand factor gene as a cause of type 3 von Willebrand disease and predisposition to inhibitor development. Blood. 2001; 98(1): 248-250.
-
(2001)
Blood
, vol.98
, Issue.1
, pp. 248-250
-
-
Surdhar, G.K.1
Enayat, M.S.2
Lawson, S.3
Williams, M.D.4
Hill, F.G.5
-
42
-
-
0033782679
-
Molecular characterization of a multiethnic group of 21 patients with type 3 von willebrand disease
-
Baronciani L, Cozzi G, Canciani M.T., et al. Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease. Thromb Haemost. 2000; 84(4): 536-540.
-
(2000)
Thromb Haemost.
, vol.84
, Issue.4
, pp. 536-540
-
-
Baronciani, L.1
Cozzi, G.2
Canciani, M.T.3
-
43
-
-
0037624499
-
Molecular defects in type 3 von Willebrand disease: Updated results from 40 multiethnic patients
-
DOI 10.1016/S1079-9796(03)00033-0
-
Baronciani L, Cozzi G, Canciani M.T., et al. Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients. Blood Cells Mol Dis. 2003; 30(3): 264-270. (Pubitemid 36539427)
-
(2003)
Blood Cells, Molecules, and Diseases
, vol.30
, Issue.3
, pp. 264-270
-
-
Baronciani, L.1
Cozzi, G.2
Canciani, M.T.3
Peyvandi, F.4
Srivastava, A.5
Federici, A.B.6
Mannucci, P.M.7
-
44
-
-
70350492506
-
A novel binding site for ADAMTS13 constitutively exposed on the surface of globular VWF
-
Zanardelli S, Chion AC, Groot E, et al. A novel binding site for ADAMTS13 constitutively exposed on the surface of globular VWF. Blood. 2009; 114(13): 2819-2828.
-
(2009)
Blood
, vol.114
, Issue.13
, pp. 2819-2828
-
-
Zanardelli, S.1
Chion, A.C.2
Groot, E.3
-
45
-
-
0036712293
-
Venous thromboembolism in von Willebrand disease
-
Mannucci PM. Venous thromboembolism in von Willebrand disease. Thromb Haemost. 2002; 88(3): 378-379. (Pubitemid 35021592)
-
(2002)
Thrombosis and Haemostasis
, vol.88
, Issue.3
, pp. 378-379
-
-
Mannucci, P.M.1
|