-
1
-
-
0023164845
-
Epidemiological investigation of von Willebrand's disease
-
Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of von Willebrand's disease. Blood 1987; 69: 454-9.
-
(1987)
Blood
, vol.69
, pp. 454-459
-
-
Rodeghiero, F.1
Castaman, G.2
Dini, E.3
-
2
-
-
0001389207
-
Prevalence of von Willebrand's disease among U.S. adults
-
Miller CH, Lenzi R, Breen C. Prevalence of von Willebrand's disease among U.S. adults. Blood 1987; 70 (Suppl. 1): 377a.
-
(1987)
Blood
, vol.70
, Issue.SUPPL. 1
-
-
Miller, C.H.1
Lenzi, R.2
Breen, C.3
-
3
-
-
0027458101
-
Prevalence of von Willebrand disease in children: A multiethnic study
-
Werner EJ, Broxson EH, Tucker EL, Giroux DS, Shults J, Abshire TC. Prevalence of von Willebrand disease in children: A multiethnic study. J Pediatr 1993; 123: 893-8.
-
(1993)
J Pediatr
, vol.123
, pp. 893-898
-
-
Werner, E.J.1
Broxson, E.H.2
Tucker, E.L.3
Giroux, D.S.4
Shults, J.5
Abshire, T.C.6
-
4
-
-
0021262077
-
Simultaneous inheritance and expression of classical haemophilia A and type II von Willebrand's disease
-
Beddall AC, Enayat SM, Williams CE, Short PE, Hill FGH. Simultaneous inheritance and expression of classical haemophilia A and type II von Willebrand's disease. J Clin Pathol 1984; 37: 1035-9.
-
(1984)
J Clin Pathol
, vol.37
, pp. 1035-1039
-
-
Beddall, A.C.1
Enayat, S.M.2
Williams, C.E.3
Short, P.E.4
Hill, F.G.H.5
-
5
-
-
0025039136
-
Congenital factor XIII deficiency associated with von Willebrand disease
-
Grand B, Riveros D, Ventura A, Maugeri N, Woods A, Lazzari M. Congenital factor XIII deficiency associated with von Willebrand disease. Am J Hematol 1990; 35: 208-9.
-
(1990)
Am J Hematol
, vol.35
, pp. 208-209
-
-
Grand, B.1
Riveros, D.2
Ventura, A.3
Maugeri, N.4
Woods, A.5
Lazzari, M.6
-
6
-
-
0027426199
-
Combined haemophilia A and type I von Willebrand's disease: A family study including an evaluation of the effects of DDAVP infusion
-
Casonato A, Pontara E, Boscaro M, Dannhauser D, Sartori MT, Girolami A. Combined haemophilia A and type I von Willebrand's disease: A family study including an evaluation of the effects of DDAVP infusion. Haematologia (Budap) 1993; 25: 57-67.
-
(1993)
Haematologia (Budap)
, vol.25
, pp. 57-67
-
-
Casonato, A.1
Pontara, E.2
Boscaro, M.3
Dannhauser, D.4
Sartori, M.T.5
Girolami, A.6
-
7
-
-
0029792533
-
Combined hereditary disorders of haemophilia B Leyden (-6 G→A) and type I von Willebrand disease
-
Pernod G, Vinciguerra C, Gaucher C, Mazurier C, Polack B, Negrier C. Combined hereditary disorders of haemophilia B Leyden (-6 G→A) and type I von Willebrand disease. Thromb Haemost 1996; 76: 151-5.
-
(1996)
Thromb Haemost
, vol.76
, pp. 151-155
-
-
Pernod, G.1
Vinciguerra, C.2
Gaucher, C.3
Mazurier, C.4
Polack, B.5
Negrier, C.6
-
8
-
-
0034764298
-
Combined hemophilia A and type 2N von Willebrand's disease: Defect of both factor VIII level and factor VIII binding capacity of von Willebrand factor
-
Casonato A, Pontara E, Sartorello F, Gemmati D, Cattini M, Girolami A. Combined hemophilia A and type 2N von Willebrand's disease: Defect of both factor VIII level and factor VIII binding capacity of von Willebrand factor. Haematologica 2001; 86: 1110-1.
-
(2001)
Haematologica
, vol.86
, pp. 1110-1111
-
-
Casonato, A.1
Pontara, E.2
Sartorello, F.3
Gemmati, D.4
Cattini, M.5
Girolami, A.6
-
9
-
-
0022497315
-
Concurrence of von Willebrand's disease and hemophilia A: Implications for carrier detection and prevalence
-
Miller CH, Hilgartner MW, Harris MB, Bussel JB, Aldedort LM. Concurrence of von Willebrand's disease and hemophilia A: Implications for carrier detection and prevalence. Am J Hum Genet 1986; 24: 83-94.
-
(1986)
Am J Hum Genet
, vol.24
, pp. 83-94
-
-
Miller, C.H.1
Hilgartner, M.W.2
Harris, M.B.3
Bussel, J.B.4
Aldedort, L.M.5
-
10
-
-
29244439008
-
The discriminant power of bleeding history for the diagnosis of type I von Willebrand disease: An international, multicenter study
-
Rodeghiero F, Castaman G, Tosetto A et. al. The discriminant power of bleeding history for the diagnosis of type I von Willebrand disease: An international, multicenter study. J Thromb Haemost 2005; 3: 2619-26.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 2619-2626
-
-
Rodeghiero, F.1
Castaman, G.2
Tosetto, A.3
-
11
-
-
0033828195
-
von Willebrand disease in a pediatric-based population-comparison of type I diagnostic criteria and use of the PFA-100 and a von Willebrand factor/collagen-binding assay
-
Dean JA, Blanchette VS, Carcao MD et al. von Willebrand disease in a pediatric-based population-comparison of type I diagnostic criteria and use of the PFA-100 and a von Willebrand factor/collagen-binding assay. Thromb Haemost 2000; 84: 401-9.
-
(2000)
Thromb Haemost
, vol.84
, pp. 401-409
-
-
Dean, J.A.1
Blanchette, V.S.2
Carcao, M.D.3
-
12
-
-
29244478325
-
Willebrand disease - The relevance of history
-
Montgomery RR. Willebrand disease - the relevance of history. J Thromb Haemost 2005; 3: 2617-8.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 2617-2618
-
-
Montgomery, R.R.1
-
13
-
-
23044515558
-
Provisional criteria for the diagnosis of VWD type 1: On behalf of the ISTH SSC subcommittee on von Willebrand factor
-
Sadler JE, Rodeghiero F. Provisional criteria for the diagnosis of VWD type 1: On behalf of the ISTH SSC subcommittee on von Willebrand factor. J Thromb Haemost 2005; 3: 775-7.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 775-777
-
-
Sadler, J.E.1
Rodeghiero, F.2
-
14
-
-
24644521462
-
Variability in clinical phenotype of severe haemophilia; the role of the first joint bleed
-
Van Dijk K, Fischer K, Van der Bom JG, Grobbee DE, Van den Berg HM. Variability in clinical phenotype of severe haemophilia; the role of the first joint bleed. Haemophilia 2005; 11: 438-43.
-
(2005)
Haemophilia
, vol.11
, pp. 438-443
-
-
Van Dijk, K.1
Fischer, K.2
Van der Bom, J.G.3
Grobbee, D.E.4
Van den Berg, H.M.5
-
15
-
-
0025189927
-
The effect of combined factor XI deficiency with von Willebrand factor abnormalities on haemorrhagic diathesis
-
Tavori S, Brenner B, Tatarsky I. The effect of combined factor XI deficiency with von Willebrand factor abnormalities on haemorrhagic diathesis. Thromb Haemost 1990; 63: 36-8.
-
(1990)
Thromb Haemost
, vol.63
, pp. 36-38
-
-
Tavori, S.1
Brenner, B.2
Tatarsky, I.3
-
16
-
-
33845796736
-
Von-Willebrand-Syndrome within the collective of haemophilic patients as reason for unexpected bleeding episodes
-
Siegmund B, Richter H, Pollmann H. Von-Willebrand-Syndrome within the collective of haemophilic patients as reason for unexpected bleeding episodes. Haemophilia 2006; 12 (Suppl. 2): 141.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 2
, pp. 141
-
-
Siegmund, B.1
Richter, H.2
Pollmann, H.3
-
17
-
-
33845774489
-
Combined diagnosis of von Willebrand disease (vWD) and hemophilia
-
Masssey G, Kuhn J, Nolte M, Dunn N, Russell E. Combined diagnosis of von Willebrand disease (vWD) and hemophilia. Haemophilia 2006; 12 (Suppl. 2): 140.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 2
, pp. 140
-
-
Masssey, G.1
Kuhn, J.2
Nolte, M.3
Dunn, N.4
Russell, E.5
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