-
1
-
-
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):454-9.
-
(1987)
Blood
, vol.69
, Issue.2
, pp. 454-459
-
-
Rodeghiero, F.1
Castaman, G.2
Dini, E.3
-
2
-
-
0032823229
-
Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation
-
Castaman G, Eikenboom JCJ, Bertina RM, Rodeghiero F. Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation. Thromb Haemost. 1999;82(3):1065-70.
-
(1999)
Thromb Haemost
, vol.82
, Issue.3
, pp. 1065-1070
-
-
Castaman, G.1
Eikenboom, J.C.J.2
Bertina, R.M.3
Rodeghiero, F.4
-
3
-
-
67149132162
-
Von Willebrand factor to the rescue
-
De Meyer SF, Deckmyn H, Vanhoorelbeke K. von Willebrand factor to the rescue. Blood. 2009;113(21):5049-57.
-
(2009)
Blood
, vol.113
, Issue.21
, pp. 5049-5057
-
-
de Meyer, S.F.1
Deckmyn, H.2
Vanhoorelbeke, K.3
-
4
-
-
3943048700
-
Treatment of von Willebrand's Disease
-
Mannucci PM. Treatment of von Willebrand's Disease. N Engl J Med. 2004; 351(7):683-94.
-
(2004)
N Engl J Med
, vol.351
, Issue.7
, pp. 683-694
-
-
Mannucci, P.M.1
-
5
-
-
2342625955
-
Management of von Willebrand disease: A guideline from the UK Haemophilia Centre Doctors' Organization
-
Pasi KJ, Collins PW, Keeling DM, Brown SA, Cumming AM, Dolan GC, et al. Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization. Haemophilia. 2004; 10(3):218-31.
-
(2004)
Haemophilia
, vol.10
, Issue.3
, pp. 218-231
-
-
Pasi, K.J.1
Collins, P.W.2
Keeling, D.M.3
Brown, S.A.4
Cumming, A.M.5
Dolan, G.C.6
-
6
-
-
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, Favaloro EJ, Hill FG, Holmberg L, et al. 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):2103-14.
-
(2006)
J Thromb Haemost
, vol.4
, Issue.10
, pp. 2103-2114
-
-
Sadler, J.E.1
Budde, U.2
Eikenboom, J.C.3
Favaloro, E.J.4
Hill, F.G.5
Holmberg, L.6
-
7
-
-
83055187115
-
Von Willebrand disease (VWD): Evidencebased diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA)
-
Nichols WL, Hultin MB, James AH, Manco- Johnson MJ, Montgomery RR, Ortel TL, et al. von Willebrand disease (VWD): evidencebased diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). Haemophilia. 2008;14(2):171-232.
-
(2008)
Haemophilia
, vol.14
, Issue.2
, pp. 171-232
-
-
Nichols, W.L.1
Hultin, M.B.2
James, A.H.3
Manco-Johnson, M.J.4
Montgomery, R.R.5
Ortel, T.L.6
-
8
-
-
66849141406
-
How I treat von Willebrand disease
-
Rodeghiero F, Castaman G, Tosetto A. How I treat von Willebrand disease. Blood. 2009; 114(6):1158-65.
-
(2009)
Blood
, vol.114
, Issue.6
, pp. 1158-1165
-
-
Rodeghiero, F.1
Castaman, G.2
Tosetto, A.3
-
9
-
-
66349136610
-
Evidence-based recommendations on the treatment of von Willebrand disease in Italy
-
Mannucci PM, Franchini M, Castaman G, Federici AB. Evidence-based recommendations on the treatment of von Willebrand disease in Italy. Blood Transf. 2009:7(2):117-26.
-
(2009)
Blood Transf
, vol.7
, Issue.2
, pp. 117-126
-
-
Mannucci, P.M.1
Franchini, M.2
Castaman, G.3
Federici, A.B.4
-
10
-
-
84877039098
-
-
Oxford, UK; Wiley-Blackwell
-
Federici AB, Lee CA, Berntorp EE, Lillicrap D, Montgomery RR. Von Willebrand disease. Oxford, UK; Wiley-Blackwell, 2011.
-
(2011)
Von Willebrand Disease
-
-
Federici, A.B.1
Lee, C.A.2
Berntorp, E.E.3
Lillicrap, D.4
Montgomery, R.R.5
-
11
-
-
0019206797
-
Application of indicators, predictors and diagnostic indices in coagulation disorders. I. Evaluation of a self-administered questionnaire with binary questions
-
Wahlberg T, Blomback M, Hall P, Axelsson G. Application of indicators, predictors and diagnostic indices in coagulation disorders. I. Evaluation of a self-administered questionnaire with binary questions. Methods Infect Med. 1980;19(4):194-200.
-
(1980)
Methods Infect Med
, vol.19
, Issue.4
, pp. 194-200
-
-
Wahlberg, T.1
Blomback, M.2
Hall, P.3
Axelsson, G.4
-
12
-
-
0029065727
-
Usefulness of patient interview in bleeding disorders
-
Sramek A, Eikenboom JC, Briet E, Vandenbroucke JP, Rosendaal FR. Usefulness of patient interview in bleeding disorders. Arch Intern Med. 1995;155(13):1409-15.
-
(1995)
Arch Intern Med
, vol.155
, Issue.13
, pp. 1409-1415
-
-
Sramek, A.1
Eikenboom, J.C.2
Briet, E.3
Vandenbroucke, J.P.4
Rosendaal, F.R.5
-
13
-
-
29244439008
-
The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: An international, multicenter study
-
Rodeghiero F, Castaman G, Tosetto A, Batlle J, Baudo F, Cappelletti A, et al. The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: an international, multicenter study. J Thromb Haemost. 2005;3(12):2619-26.
-
(2005)
J Thromb Haemost
, vol.3
, Issue.12
, pp. 2619-2626
-
-
Rodeghiero, F.1
Castaman, G.2
Tosetto, A.3
Batlle, J.4
Baudo, F.5
Cappelletti, A.6
-
14
-
-
43249098361
-
Evidence-based diagnosis of type 1 von Willebrand disease: A Bayes theorem approach
-
Tosetto A, Castaman G, Rodeghiero F. Evidence-based diagnosis of type 1 von Willebrand disease: a Bayes theorem approach. Blood. 2008;111(8):3998-4003.
-
(2008)
Blood
, vol.111
, Issue.8
, pp. 3998-4003
-
-
Tosetto, A.1
Castaman, G.2
Rodeghiero, F.3
-
15
-
-
43149083497
-
Bleeding scores in inherited bleeding disorders: Clinical or research tools?
-
Tosetto A, Rodeghiero F, Castaman G. Bleeding scores in inherited bleeding disorders: clinical or research tools? Haemophilia. 2008;14(3):415-22.
-
(2008)
Haemophilia
, vol.14
, Issue.3
, pp. 415-422
-
-
Tosetto, A.1
Rodeghiero, F.2
Castaman, G.3
-
16
-
-
77956493323
-
ISTH/SSC bleeding assessment tool: A standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders
-
Rodeghiero F, Tosetto A, Abshire T, Arnold DM, Coller B, James P, et al. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders. J Thromb Haemost. 2010;8(9):2063-5.
-
(2010)
J Thromb Haemost
, vol.8
, Issue.9
, pp. 2063-2065
-
-
Rodeghiero, F.1
Tosetto, A.2
Abshire, T.3
Arnold, D.M.4
Coller, B.5
James, P.6
-
17
-
-
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, Goodeve A, Federici AB, Budde U, 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(4):766-73.
-
(2006)
J Thromb Haemost
, vol.4
, Issue.4
, pp. 766-773
-
-
Tosetto, A.1
Rodeghiero, F.2
Castaman, G.3
Goodeve, A.4
Federici, A.B.5
Budde, U.6
-
18
-
-
33845967766
-
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
-
Goodeve A, Eikenboom J, Castaman G, Rodeghiero F, Federici AB, Batlle J, et al. Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD). Blood. 2007;109(1):112-21.
-
(2007)
Blood
, vol.109
, Issue.1
, pp. 112-121
-
-
Goodeve, A.1
Eikenboom, J.2
Castaman, G.3
Rodeghiero, F.4
Federici, A.B.5
Batlle, J.6
-
19
-
-
77953800564
-
Quantitation of bleeding symptoms in children with von Willebrand disease: Use of a standardized pediatric bleeding questionnaire
-
Biss TT, Blanchette VS, Clark SD, Bowman M, Wakefield CD, Silva M, et al. Quantitation of bleeding symptoms in children with von Willebrand disease: use of a standardized pediatric bleeding questionnaire. J Thromb Haemost. 2010;8(6):950-6.
-
(2010)
J Thromb Haemost
, vol.8
, Issue.6
, pp. 950-956
-
-
Biss, T.T.1
Blanchette, V.S.2
Clark, S.D.3
Bowman, M.4
Wakefield, C.D.5
Silva, M.6
-
20
-
-
79955396907
-
Bleeding tendency and efficacy of anti-haemorrhagic treatments in patients with type 1 von Willebrand disease and increased von Willebrand factor clearance
-
Castaman G, Tosetto A, Federici AB, Rodeghiero F. Bleeding tendency and efficacy of anti-haemorrhagic treatments in patients with type 1 von Willebrand disease and increased von Willebrand factor clearance. Thromb Haemost. 2011;105(4):647-54.
-
(2011)
Thromb Haemost
, vol.105
, Issue.4
, pp. 647-654
-
-
Castaman, G.1
Tosetto, A.2
Federici, A.B.3
Rodeghiero, F.4
-
21
-
-
84859169124
-
Different bleeding risk in type 2 A and 2 M Von Willebrand disease: A two-year prospective study in 107 patients
-
Castaman G, Federici AB, Tosetto A, La Marca S, Stufano F, Mannucci PM, et al. Different bleeding risk in type 2 A and 2 M Von Willebrand disease: a two-year prospective study in 107 patients. J Thromb Haemost. 2012;10(4):632-8.
-
(2012)
J Thromb Haemost
, vol.10
, Issue.4
, pp. 632-638
-
-
Castaman, G.1
Federici, A.B.2
Tosetto, A.3
la Marca, S.4
Stufano, F.5
Mannucci, P.M.6
-
22
-
-
0026011654
-
Human von Willebrand factor gene and pseudogene: Structural analysis and differentiation by polymerase chain reaction
-
Mancuso DJ, Tuley EA, Westfield LA et al. Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction. Biochemistry 1991;30(1):253-69.
-
(1991)
Biochemistry
, vol.30
, Issue.1
, pp. 253-269
-
-
Mancuso, D.J.1
Tuley, E.A.2
Westfield, L.A.3
-
23
-
-
77952581903
-
The genetic basis of von Willebrand disease
-
Goodeve A. The genetic basis of von Willebrand disease. Blood Rev. 2010;24(3): 123-34.
-
(2010)
Blood Rev
, vol.24
, Issue.3
, pp. 123-134
-
-
Goodeve, A.1
-
24
-
-
51249102362
-
The molecular analysis of von Willebrand disease: A guideline from the UK Haemophilia Centre Doctors' Organisation Haemophilia Genetics Laboratory Network
-
Keeney S, Bowen D, Cumming A, Enayat S, Goodeve A, Hill F. The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organisation Haemophilia Genetics Laboratory Network. Haemophilia. 2008; 14(4):1099-11.
-
(2008)
Haemophilia
, vol.14
, Issue.4
, pp. 1099-1111
-
-
Keeney, S.1
Bowen, D.2
Cumming, A.3
Enayat, S.4
Goodeve, A.5
Hill, F.6
-
25
-
-
84877020937
-
Laboratory diagnosis of von Willebrand disease: The phenotype
-
Federici AB, Lee CA, Berntorp EE, Lillicrap D, Montgomery RR, Oxford, UK; Wiley-Blackwell
-
Budde U, Favaloro EJ. Laboratory diagnosis of von Willebrand disease: the phenotype. In Federici AB, Lee CA, Berntorp EE, Lillicrap D, Montgomery RR (eds). Von Willebrand disease. Oxford, UK; Wiley-Blackwell, 2011, 100-13.
-
(2011)
Von Willebrand Disease
, pp. 100-113
-
-
Budde, U.1
Favaloro, E.J.2
-
26
-
-
0024420764
-
Consistency of responses to repeated DDAVP infusions in patients with von Willebrand's disease and hemophilia A
-
Rodeghiero F, Castaman G, Di Bona E, Ruggeri M. Consistency of responses to repeated DDAVP infusions in patients with von Willebrand's disease and hemophilia A. Blood. 1989;74(6):1997-2000.
-
(1989)
Blood
, vol.74
, Issue.6
, pp. 1997-2000
-
-
Rodeghiero, F.1
Castaman, G.2
Di Bona, E.3
Ruggeri, M.4
-
27
-
-
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, Lee CA, Scharrer I, Goudemand J, 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 (6);103: 2032-8.
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2032-2038
-
-
Federici, A.B.1
Mazurier, C.2
Berntorp, E.3
Lee, C.A.4
Scharrer, I.5
Goudemand, J.6
-
28
-
-
43549097149
-
Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): Results from the European Study MCMDM-1VWD
-
Castaman G, Lethagen S, Federici AB, Tosetto A, Goodeve A, Budde U, et al. Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD. Blood. 2008(7);111: 3531-9.
-
(2008)
Blood
, vol.111
, Issue.7
, pp. 3531-3539
-
-
Castaman, G.1
Lethagen, S.2
Federici, A.B.3
Tosetto, A.4
Goodeve, A.5
Budde, U.6
-
29
-
-
67849111584
-
Reduced von Willebrand factor survival in von Willebrand disease: Pathophysiologic and clinical relevance
-
Castaman G, Tosetto A, Rodeghiero F. Reduced von Willebrand factor survival in von Willebrand disease: pathophysiologic and clinical relevance. J Thomb Haemost. 2009;7:(Suppl 1):71-4.
-
(2009)
J Thomb Haemost
, vol.7
, Issue.SUPPL. 1
, pp. 71-74
-
-
Castaman, G.1
Tosetto, A.2
Rodeghiero, F.3
-
30
-
-
0029967568
-
Desmopressin and type II B von Willebrand disease
-
Castaman G, Rodeghiero F. Desmopressin and type II B von Willebrand disease. Hemophilia. 1996;2(2):73-6.
-
(1996)
Hemophilia
, vol.2
, Issue.2
, pp. 73-76
-
-
Castaman, G.1
Rodeghiero, F.2
-
31
-
-
60249092963
-
Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: A cohort study of 67 patients
-
Federici AB, Mannucci PM, Castaman G, Baronciani L, Bucciarelli P, Canciani MT, et al. Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients. Blood. 2009;113(5):526-34.
-
(2009)
Blood
, vol.113
, Issue.5
, pp. 526-534
-
-
Federici, A.B.1
Mannucci, P.M.2
Castaman, G.3
Baronciani, L.4
Bucciarelli, P.5
Canciani, M.T.6
-
32
-
-
0026713114
-
Patterns of development of tachyphylaxis in patients with haemophilia and von Willebrand disease after repeated doses of desmopressin (DDAVP)
-
Mannucci PM, Bettega D, Cattaneo M. Patterns of development of tachyphylaxis in patients with haemophilia and von Willebrand disease after repeated doses of desmopressin (DDAVP). Br J Haematol. 1992;82(1):87-93.
-
(1992)
Br J Haematol
, vol.82
, Issue.1
, pp. 87-93
-
-
Mannucci, P.M.1
Bettega, D.2
Cattaneo, M.3
-
33
-
-
0024410234
-
Hyponatremia and seizures in young children given DDAVP
-
Smith TJ, Gill JC, Ambruso DR, Hathaway WE. Hyponatremia and seizures in young children given DDAVP. Am J Hematol. 1989; 31(3):199-202.
-
(1989)
Am J Hematol
, vol.31
, Issue.3
, pp. 199-202
-
-
Smith, T.J.1
Gill, J.C.2
Ambruso, D.R.3
Hathaway, W.E.4
-
34
-
-
0023835090
-
Myocardial infarction in a patient with hemophilia treated with DDAVP
-
Bond L, Bevan D. Myocardial infarction in a patient with hemophilia treated with DDAVP. N Eng J Med. 1988;318(2):121.
-
(1988)
N Eng J Med
, vol.318
, Issue.2
, pp. 121
-
-
Bond, L.1
Bevan, D.2
-
35
-
-
0023875934
-
Thrombosis following desmopressin for uremic bleeding
-
Byrnes JJ, Larcada A, Moake JL. Thrombosis following desmopressin for uremic bleeding. Am J Hematol. 1988;28(1):63-5.
-
(1988)
Am J Hematol
, vol.28
, Issue.1
, pp. 63-65
-
-
Byrnes, J.J.1
Larcada, A.2
Moake, J.L.3
-
36
-
-
17044373272
-
Use of desmopressin (DDAVP) during early pregnancy in factor VIII-deficient women
-
Mannucci PM. Use of desmopressin (DDAVP) during early pregnancy in factor VIII-deficient women. Blood. 2005; 105(8):3382.
-
(2005)
Blood
, vol.105
, Issue.8
, pp. 3382
-
-
Mannucci, P.M.1
-
37
-
-
77953210923
-
Pregnancy and delivery in women with von Willebrand's disease and different von Willebrand factor mutations
-
Castaman G, Tosetto A, Rodeghiero F. Pregnancy and delivery in women with von Willebrand's disease and different von Willebrand factor mutations. Haematologica. 2010; 95(6) 963-9.
-
(2010)
Haematologica
, vol.95
, Issue.6
, pp. 963-969
-
-
Castaman, G.1
Tosetto, A.2
Rodeghiero, F.3
-
38
-
-
0141955859
-
Immunization of patients with bleeding disorders
-
Makris M, Conlon CP, Watson HG. Immunization of patients with bleeding disorders. Haemophilia. 2003;9(5):541-6.
-
(2003)
Haemophilia
, vol.9
, Issue.5
, pp. 541-546
-
-
Makris, M.1
Conlon, C.P.2
Watson, H.G.3
-
39
-
-
63349109590
-
Hepatitis A and B immunization for individuals with inherited bleeding disorders
-
Steele M, Cochrane A, Wakefield C, Stain AM, Ling S, Blanchette V, Gold R, Ford-Jones L. Hepatitis A and B immunization for individuals with inherited bleeding disorders. Haemophilia. 2009;15(2):437-47.
-
(2009)
Haemophilia
, vol.15
, Issue.2
, pp. 437-447
-
-
Steele, M.1
Cochrane, A.2
Wakefield, C.3
Stain, A.M.4
Ling, S.5
Blanchette, V.6
Gold, R.7
Ford-Jones, L.8
-
40
-
-
66949168185
-
The safety of plasma-derived von Willebrand/factor VIII concentrates in the management of inherited von Willebrand disease
-
Federici AB. The safety of plasma-derived von Willebrand/factor VIII concentrates in the management of inherited von Willebrand disease. Expert Opin Drug Saf. 2009(2); 8: 203-10.
-
(2009)
Expert Opin Drug Saf
, vol.8
, Issue.2
, pp. 203-210
-
-
Federici, A.B.1
-
41
-
-
84877028333
-
The use of plasma- derived concentrates
-
Federici AB, Lee CA, Berntorp EE, Lillicrap D, Mongomery RR., Oxford, UK; Wiley-Blackwell
-
Mannucci PM, Franchini M. The use of plasma- derived concentrates. In: Federici AB, Lee CA, Berntorp EE, Lillicrap D, Mongomery RR. Von Willebrand disease. Oxford, UK; Wiley-Blackwell, 2011:200-6.
-
(2011)
Von Willebrand Disease
, pp. 200-206
-
-
Mannucci, P.M.1
Franchini, M.2
-
42
-
-
79959792971
-
Treatment of von Willebrand disease with FVIII/VWF concentrates
-
Castaman G. Treatment of von Willebrand disease with FVIII/VWF concentrates. Blood Transf. 2011;9(Suppl 2):s9-s13.
-
(2011)
Blood Transf
, vol.9
, Issue.SUPPL. 2
-
-
Castaman, G.1
-
43
-
-
28444472737
-
Pharmacokinetic studies on Wilfactin, a von Willebrand factor concentrate with a low factor VIII content treated with three virusinactivation/ removal methods
-
Goudemand J, Scharrer I, Berntorp E, Lee CA, Borel-Derlon A, Stieltjes N, et al. Pharmacokinetic studies on Wilfactin, a von Willebrand factor concentrate with a low factor VIII content treated with three virusinactivation/ removal methods. J Thromb Haemost. 2005;3(10):2219-27.
-
(2005)
J Thromb Haemost
, 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
-
44
-
-
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, Goudemand J, Lee CA, Scharrer I, 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):1115-24.
-
(2007)
J Thromb Haemost
, vol.5
, Issue.6
, pp. 1115-1124
-
-
Borel-Derlon, A.1
Federici, A.B.2
Roussel-Robert, V.3
Goudemand, J.4
Lee, C.A.5
Scharrer, I.6
-
45
-
-
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, Shields ML, Smith MP. Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease. Thromb Haemost. 2002;88(3):387-8.
-
(2002)
Thromb Haemost
, vol.88
, Issue.3
, pp. 387-388
-
-
Makris, M.1
Colvin, B.2
Gupta, V.3
Shields, M.L.4
Smith, M.P.5
-
46
-
-
0036712293
-
Venous thromboembolism in von Willebrand disease
-
Mannucci PM. Venous thromboembolism in von Willebrand disease. Thromb Haemost. 2002;88(3):378-9.
-
(2002)
Thromb Haemost
, vol.88
, Issue.3
, pp. 378-379
-
-
Mannucci, P.M.1
-
47
-
-
19944364505
-
Long-term prophylaxis in von Willebrand disease
-
Berntorp E, Petrini P. Long-term prophylaxis in von Willebrand disease. Blood Coag Fibrinol. 2005;16(Suppl 1):S23-6.
-
(2005)
Blood Coag Fibrinol
, vol.16
, Issue.SUPPL. 1
-
-
Berntorp, E.1
Petrini, P.2
-
48
-
-
37149005797
-
Highly purified VWF/FVIII concentrates in the treatment and prophylaxis of von Willebrand disease. The PRO.WILL study
-
Federici AB. Highly purified VWF/FVIII concentrates in the treatment and prophylaxis of von Willebrand disease. The PRO.WILL study. Haemophilia. 2007;13(Suppl 5):15-24.
-
(2007)
Haemophilia
, vol.13
, Issue.SUPPL. 5
, pp. 15-24
-
-
Federici, A.B.1
-
49
-
-
84870998006
-
Prophylaxis in severe forms of von Willebrand's disease: Results from the von Willebrand disease prophylaxis network (VWD PN)
-
Abshire TC, Federici AB, Alvarez MT, Bowen J, Carcao MD, Cox Gill J, et al. Prophylaxis in severe forms of von Willebrand's disease: results from the von Willebrand disease prophylaxis network (VWD PN). Haemophilia. 2013;19(1):76-81.
-
(2013)
Haemophilia
, vol.19
, Issue.1
, pp. 76-81
-
-
Abshire, T.C.1
Federici, A.B.2
Alvarez, M.T.3
Bowen, J.4
Carcao, M.D.5
Cox Gill, J.6
-
50
-
-
0023469711
-
Lifethreatening reaction to factor VIII concentrate in a patient with severe von Willebrand disease and alloantibodies to von Willebrand factor
-
Mannucci PM, Tamaro G, Narchi G, Candotti G, Federici A, Altieri D, et al. Lifethreatening reaction to factor VIII concentrate in a patient with severe von Willebrand disease and alloantibodies to von Willebrand factor. Eur J Hematol. 1987;39(5):467-70.
-
(1987)
Eur J Hematol
, vol.39
, Issue.5
, pp. 467-470
-
-
Mannucci, P.M.1
Tamaro, G.2
Narchi, G.3
Candotti, G.4
Federici, A.5
Altieri, D.6
-
51
-
-
79955643645
-
Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population
-
Mohl A, Boda Z, Jager R, Losonczy H, Marosi A, Masszi T, et al. Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population. J Thromb Haemost. 2011;9(5):945-52.
-
(2011)
J Thromb Haemost
, vol.9
, Issue.5
, pp. 945-952
-
-
Mohl, A.1
Boda, Z.2
Jager, R.3
Losonczy, H.4
Marosi, A.5
Masszi, T.6
-
52
-
-
0029872095
-
Use of recombinant factor VIIa (NovoSeven) in the treatment of two patients with type III von Willebrand's disease and an inhibitor against von Willebrand factor
-
Ciavarella N, Schiavoni M, Valenzano E, Mangini F, Inchingolo F. Use of recombinant factor VIIa (NovoSeven) in the treatment of two patients with type III von Willebrand's disease and an inhibitor against von Willebrand factor. Haemostasis. 1996;26 (Suppl 1):10-4.
-
(1996)
Haemostasis
, vol.26
, Issue.SUPPL. 1
, pp. 10-14
-
-
Ciavarella, N.1
Schiavoni, M.2
Valenzano, E.3
Mangini, F.4
Inchingolo, F.5
-
53
-
-
43149111831
-
Treatment for patients with type 3 von Willebrand disease and alloantibodies: A case report
-
Franchini M, Gandini G, Giuffrida A, De Gironcoli M, Federici AB. Treatment for patients with type 3 von Willebrand disease and alloantibodies: a case report. Haemophilia. 2008;14(3):645-6.
-
(2008)
Haemophilia
, vol.14
, Issue.3
, pp. 645-646
-
-
Franchini, M.1
Gandini, G.2
Giuffrida, A.3
de Gironcoli, M.4
Federici, A.B.5
-
54
-
-
0025878651
-
Hemostatic effect of normal platelet transfusion in severe von Willebrand disease patients
-
Castillo R, Monteagudo J, Escolar G, Ordinas A, Magallón M, Martín Villar J. Hemostatic effect of normal platelet transfusion in severe von Willebrand disease patients. Blood. 1991;77(9):1901-5.
-
(1991)
Blood
, vol.77
, Issue.9
, pp. 1901-1905
-
-
Castillo, R.1
Monteagudo, J.2
Escolar, G.3
Ordinas, A.4
Magallón, M.5
Martín Villar, J.6
-
55
-
-
0032560732
-
Hemostatic drugs
-
Mannucci PM. Hemostatic drugs. N Eng J Med. 1998;339(4):245-53.
-
(1998)
N Eng J Med
, vol.339
, Issue.4
, pp. 245-253
-
-
Mannucci, P.M.1
-
56
-
-
0031892630
-
Pregnancy in women with von Willebrand's disease or factor XI deficiency
-
Kadir RA, Lee CA, Sabin CA, Pollard D, Economides DL. Pregnancy in women with von Willebrand's disease or factor XI deficiency. Br J Obstet Gynaecol. 1998;105(3): 314-21.
-
(1998)
Br J Obstet Gynaecol
, vol.105
, Issue.3
, pp. 314-321
-
-
Kadir, R.A.1
Lee, C.A.2
Sabin, C.A.3
Pollard, D.4
Economides, D.L.5
-
57
-
-
80155208168
-
Gynaecological and obstetric bleeding in moderate and severe von Willebrand disease
-
De Wee EM, Knol HM, Mauser-Bunschoten EP, van der Bom JG, Eikenboom JC, Fijnvandraat K, et al. Gynaecological and obstetric bleeding in moderate and severe von Willebrand disease. Thromb Haemost. 2011;106(5):885-92.
-
(2011)
Thromb Haemost
, vol.106
, Issue.5
, pp. 885-892
-
-
de Wee, E.M.1
Knol, H.M.2
Mauser-Bunschoten, E.P.3
van der Bom, J.G.4
Eikenboom, J.C.5
Fijnvandraat, K.6
-
58
-
-
10844220754
-
The use of levonorgestrel-releasing intrauterine system for treatment of menorrhagia in women with inherited bleeding disorders
-
Kingman CE, Kadir RA, Lee CA, Economides DL. The use of levonorgestrel-releasing intrauterine system for treatment of menorrhagia in women with inherited bleeding disorders. Br J Obstet Gynaecol. 2004;111(12): 1425-8.
-
(2004)
Br J Obstet Gynaecol
, vol.111
, Issue.12
, pp. 1425-1428
-
-
Kingman, C.E.1
Kadir, R.A.2
Lee, C.A.3
Economides, D.L.4
-
59
-
-
0032515596
-
Frequency of inherited bleeding disorders in women with menorrhagia
-
Kadir RA, Economides DL, Sabin CA, Owens D, Lee CA. Frequency of inherited bleeding disorders in women with menorrhagia. Lancet. 1998,351(9101):485-9.
-
(1998)
Lancet
, vol.351
, Issue.9101
, pp. 485-489
-
-
Kadir, R.A.1
Economides, D.L.2
Sabin, C.A.3
Owens, D.4
Lee, C.A.5
-
60
-
-
0023610642
-
Von Willebrand's disease presenting as thrombocytopenia during pregnancy
-
Giles AR, Hoogendoorn H, Benford K. Type IIB von Willebrand's disease presenting as thrombocytopenia during pregnancy. Br J Haematol. 1987;67(3):349-53.
-
(1987)
Br J Haematol
, vol.67
, Issue.3
, pp. 349-353
-
-
Giles, A.R.1
Hoogendoorn, H.2
Benford, K.3
Type, I.I.B.4
-
61
-
-
34249929900
-
Evaluation of the clinical safety of desmopressin during pregnancy in women with a low plasmatic von Willebrand factor level and bleeding history
-
Sánchez-Luceros A, Meschengieser SS, Turdó K, Arizó A, Woods AI, Casais P, et al. Evaluation of the clinical safety of desmopressin during pregnancy in women with a low plasmatic von Willebrand factor level and bleeding history. Thromb Res. 2007; 120(3):387-90.
-
(2007)
Thromb Res
, vol.120
, Issue.3
, pp. 387-390
-
-
Sánchez-Luceros, A.1
Meschengieser, S.S.2
Turdó, K.3
Arizó, A.4
Woods, A.I.5
Casais, P.6
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