-
1
-
-
0023164845
-
Epidemiological investigations 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;69:454-9. (Pubitemid 17022013)
-
(1987)
Blood
, vol.69
, Issue.2
, pp. 454-459
-
-
Rodeghiero, F.1
Castaman, G.2
Dini, E.3
-
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;84:160-74. (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
-
-
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)
J Thromb Haemost
, vol.4
, pp. 766-773
-
-
Tosetto, A.1
Rodeghiero, F.2
Castaman, G.3
-
4
-
-
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, 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;8:2063-5.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 2063-2065
-
-
Rodeghiero, F.1
Tosetto, A.2
Abshire, T.3
-
5
-
-
77953800564
-
Quantitation of bleeding symptoms in children with von Willebrand disease: Use of a standardized pediatric bleeding questionnaire
-
Biss TT, Blanchette VS, Clark DS, et al. Quantitation of bleeding symptoms in children with von Willebrand disease: use of a standardized pediatric bleeding questionnaire. J Thromb Haemost. 2010;8:950-6.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 950-956
-
-
Biss, T.T.1
Blanchette, V.S.2
Clark, D.S.3
-
6
-
-
33748802581
-
Update on the pathophysiology and classification of von Willebrand disease: A report of the Subcommittee on von Willebrand factor
-
DOI 10.1111/j.1538-7836.2006.02146.x
-
Sadler JE, Budde U, Eikenboom JC, 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;4:2103-14. (Pubitemid 44403432)
-
(2006)
Journal of Thrombosis and Haemostasis
, vol.4
, Issue.10
, pp. 2103-2114
-
-
Sadler, J.E.1
Budde, U.2
Eikenboom, J.C.J.3
Favaloro, E.J.4
Hill, F.G.H.5
Holmberg, L.6
Ingerslev, J.7
Lee, C.A.8
Lillicrap, D.9
Mannucci, P.M.10
Mazurier, C.11
Meyer, D.12
Nichols, W.L.13
Nishino, M.14
Peake, I.R.15
Rodeghiero, F.16
Schneppenheim, R.17
Ruggeri, Z.M.18
Srivastava, A.19
Montgomery, R.R.20
Federici, A.B.21
more..
-
9
-
-
0017336844
-
1 Deamino 8 D arginine vasopressin: A new pharmacological approach to the management of haemophilia and von Willebrand's disease
-
Mannucci PM, Ruggeri ZM, Pareti FI, Capitanio A. 1-Deamino-8-darginine vasopressin: a new pharmacological approach to the management of haemophilia and von Willebrands' diseases. Lancet. 1977;1(8017):869-72. (Pubitemid 8079684)
-
(1977)
Lancet
, vol.1
, Issue.8017
, pp. 869-872
-
-
Mannucci, P.M.1
Ruggeri, Z.M.2
Pareti, F.I.3
Capitanio, A.4
-
10
-
-
0142197167
-
Cellular mechanisms of the hemostatic effects of desmopressin (DDAVP)
-
Kaufmann JE, Vischer UM. Cellular mechanisms of the hemostatic effects of desmopressin (DDAVP). J Thromb Haemost. 2003;1:682-9.
-
(2003)
J Thromb Haemost
, vol.1
, pp. 682-689
-
-
Kaufmann, J.E.1
Vischer, U.M.2
-
11
-
-
0020591405
-
Platelet aggregation induced by 1-desamino-8-D-arginine vasopressin (DDAVP) in type IIB von Willebrand's disease
-
Holmberg L, Nilsson IM, Borge L, Gunnarsson M, Sjorin E. Platelet aggregation induced by 1-desamino-8-D-arginine vasopressin (DDAVP) in Type IIB von Willebrand's disease. N Engl J Med. 1983;309:816-21. (Pubitemid 13005034)
-
(1983)
New England Journal of Medicine
, vol.309
, Issue.14
, pp. 816-821
-
-
Holmberg, L.1
Nilsson, I.M.2
Borge, L.3
-
12
-
-
11044235267
-
Clinical diagnosis of von Willebrand disease
-
Federici AB. Clinical diagnosis of von Willebrand disease. Haemophilia. 2004;10(Suppl 4):169-76. (Pubitemid 40045438)
-
(2004)
Haemophilia, Supplement
, vol.10
, Issue.4
, pp. 169-176
-
-
Federici, A.B.1
-
13
-
-
84867247388
-
Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease
-
De Wee EM, Sanders YV, Mauser-Bunschoten EP, et al. Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease. Thromb Haemost. 2012;108:683-92.
-
(2012)
Thromb Haemost
, vol.108
, pp. 683-692
-
-
De Wee, E.M.1
Sanders, Y.V.2
Mauser-Bunschoten, E.P.3
-
14
-
-
80155208168
-
Gynaecological and obstetric bleeding in moderate and severe von Willebrand disease
-
De Wee EM, Knol HM, Mauser-Bunschoten EP, et al. Gynaecological and obstetric bleeding in moderate and severe von Willebrand disease. Thromb Haemost. 2011;106:885-92.
-
(2011)
Thromb Haemost
, vol.106
, pp. 885-892
-
-
De Wee, E.M.1
Knol, H.M.2
Mauser-Bunschoten, E.P.3
-
15
-
-
77957755712
-
Routine evaluation and treatment of unexplained menorrhagia: Do we consider haemostatic disorders?
-
Knol HM, Bogchelman DH, Kluin-Nelemans HC, van der Zee AG, van der Meer J, Meijer K. Routine evaluation and treatment of unexplained menorrhagia: do we consider haemostatic disorders? Eur J Obstet Gynecol Reprod Biol. 2010;152:191-4.
-
(2010)
Eur J Obstet Gynecol Reprod Biol
, vol.152
, pp. 191-194
-
-
Knol, H.M.1
Bogchelman, D.H.2
Kluin-Nelemans, H.C.3
Van Der Zee, A.G.4
Van Der Meer, J.5
Meijer, K.6
-
16
-
-
25444487788
-
Postpartum hemorrhage and transfusion of blood and blood components
-
DOI 10.1097/01.ogx.0000180909.31293.cf
-
Jansen AJ, van Rhenen DJ, Steegers EA, Duvekot JJ. Postpartum hemorrhage and transfusion of blood and blood components. Obstet Gynecol Surv. 2005;60:663-71. (Pubitemid 41368533)
-
(2005)
Obstetrical and Gynecological Survey
, vol.60
, Issue.10
, pp. 663-671
-
-
Jansen, A.J.G.1
Van Rhenen, D.J.2
Steegers, E.A.P.3
Duvekot, J.J.4
-
17
-
-
84860341625
-
Effect of fibrinolysis on bleeding phenotype in moderate and severe von Willebrand disease
-
De Wee EM, Klaij K, Eikenboom HC, van der Bom JG, Fijnvandraat K, Laros-van Gorkom BA, et al. Effect of fibrinolysis on bleeding phenotype in moderate and severe von Willebrand disease. Haemophilia. 2012;18:444-51.
-
(2012)
Haemophilia
, vol.18
, pp. 444-451
-
-
De Wee, E.M.1
Klaij, K.2
Eikenboom, H.C.3
Van Der Bom, J.G.4
Fijnvandraat, K.5
Laros-van Gorkom, B.A.6
-
18
-
-
79952058550
-
Impact of von Willebrand disease on health-related quality of life in a pediatric population
-
De Wee EM, Fijnvandraat K, de Goede-Bolder A, et al. Impact of von Willebrand disease on health-related quality of life in a pediatric population. J Thromb Haemost. 2011;9:502-9.
-
(2011)
J Thromb Haemost
, vol.9
, pp. 502-509
-
-
De Wee, E.M.1
Fijnvandraat, K.2
De Goede-Bolder, A.3
-
19
-
-
77955042246
-
Health-related quality of life among adult patients with moderate and severe von Willebrand disease
-
De Wee EM, Mauser-Bunschoten EP, van der Bom JG, et al. Health-related quality of life among adult patients with moderate and severe von Willebrand disease. J Thromb Haemost. 2010;8:1492-9.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 1492-1499
-
-
De Wee, E.M.1
Mauser-Bunschoten, E.P.2
Van Der Bom, J.G.3
-
20
-
-
0033432718
-
Assessing health-related quality-of-life in individuals with haemophilia
-
DOI 10.1046/j.1365-2516.1999.00347.x
-
Miners AH, Sabin CA, Tolley KH, Jenkinson C, Kind P, Lee CA. Assessing health-related quality-of-life in individuals with haemophilia. Haemophilia. 1999;5:378-85. (Pubitemid 30003764)
-
(1999)
Haemophilia
, vol.5
, Issue.6
, pp. 378-385
-
-
Miners, A.H.1
Sabin, C.A.2
Tolley, K.H.3
Jenkinson, C.4
Kind, P.5
Lee, C.A.6
-
21
-
-
79955656759
-
Genetic determinants of von Willebrand factor levels and activity in relation to the risk of cardiovascular disease: A review
-
Van Schie MC, van Loon JE, de Maat MP, Leebeek FW. Genetic determinants of von Willebrand factor levels and activity in relation to the risk of cardiovascular disease: a review. J Thromb Haemost. 2011;9:899-908.
-
(2011)
J Thromb Haemost
, vol.9
, pp. 899-908
-
-
Van Schie, M.C.1
Van Loon, J.E.2
De Maat, M.P.3
Leebeek, F.W.4
-
22
-
-
59049090849
-
Cardiovascular disease in patients with hemophilia
-
Tuinenburg A, Mauser-Bunschoten EP, Verhaar MC, Biesma DH, Schutgens RE. Cardiovascular disease in patients with hemophilia. J Thromb Haemost. 2009;7:247-54.
-
(2009)
J Thromb Haemost
, vol.7
, pp. 247-254
-
-
Tuinenburg, A.1
Mauser-Bunschoten, E.P.2
Verhaar, M.C.3
Biesma, D.H.4
Schutgens, R.E.5
-
23
-
-
84877915937
-
Reduced prevalence of arterial thrombosis in von Willebrand disease
-
Sanders YV, Eikenboom J, de Wee EM, et al. Reduced prevalence of arterial thrombosis in von Willebrand disease. J Thromb Haemost. 2013;11:845-54.
-
(2013)
J Thromb Haemost
, vol.11
, pp. 845-854
-
-
Sanders, Y.V.1
Eikenboom, J.2
De Wee, E.M.3
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