-
2
-
-
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, 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 (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..
-
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 4 766-773
-
(2006)
J Thromb Haemost
, vol.4
, Issue.4
, pp. 766-773
-
-
Tosetto, A.1
Rodeghiero, F.2
Castaman, G.3
-
4
-
-
56749160315
-
Generation and validation of the condensed MCMDM-1VWD bleeding questionnaire for von Willebrand disease
-
Bowman M, Mundell G, Grabell J et al. Generation and validation of the condensed MCMDM-1VWD bleeding questionnaire for von Willebrand disease. J Thromb Haemost 2008 6 12 2062-2066
-
(2008)
J Thromb Haemost
, vol.6
, Issue.12
, pp. 2062-2066
-
-
Bowman, M.1
Mundell, G.2
Grabell, J.3
-
5
-
-
0033926486
-
Desmopressin (DDAVP) in the treatment of bleeding disorders: The first twenty years
-
DOI 10.1046/j.1365-2516.2000.00059.x
-
Mannucci PM. Desmopressin (DDAVP) in the treatment of bleeding disorders: the first twenty years. Haemophilia 2000 6 Suppl 1 60-67 (Pubitemid 30468295)
-
(2000)
Haemophilia
, vol.6
, Issue.SUPPL. 1
, pp. 60-67
-
-
Mannucci, P.M.1
-
6
-
-
34748846640
-
Prevalence of von Willebrand disease in the Nordic region
-
Berntorp E, Önundarson PT. Prevalence of von Willebrand disease in the Nordic region. Haematologica Rep 2005 1 4-6
-
(2005)
Haematologica Rep
, vol.1
, pp. 4-6
-
-
Berntorp, E.1
Önundarson, P.T.2
-
7
-
-
38549157588
-
An update on the von Willebrand factor collagen binding assay: 21 Years of age and beyond adolescence but not yet a mature adult
-
DOI 10.1055/s-2007-1000364
-
Favaloro EJ. An update on the von Willebrand factor collagen binding assay: 21 years of age and beyond adolescence but not yet a mature adult. Semin Thromb Hemost 2007 33 8 727-744 (Pubitemid 351158442)
-
(2007)
Seminars in Thrombosis and Hemostasis
, vol.33
, Issue.8
, pp. 727-744
-
-
Favaloro, E.J.1
-
8
-
-
33747161013
-
Von Willebrand factor collagen binding assay in von Willebrand disease type 2A, 2B, and 2M [8]
-
DOI 10.1111/j.1538-7836.2006.02069.x
-
Baronciani L, Federici AB, Cozzi G, Canciani MT, Mannucci PM. von Willebrand factor collagen binding assay in von Willebrand disease type 2A, 2B, and 2M. J Thromb Haemost 2006 4 9 2088-2090 (Pubitemid 44226803)
-
(2006)
Journal of Thrombosis and Haemostasis
, vol.4
, Issue.9
, pp. 2088-2090
-
-
Baronciani, L.1
Federici, A.B.2
Cozzi, G.3
Canciani, M.T.4
Mannucci, P.M.5
-
9
-
-
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)
-
DOI 10.1182/blood-2006-05-020784
-
Goodeve A, Eikenboom J, Castaman G 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 1 112-121 (Pubitemid 46053051)
-
(2007)
Blood
, vol.109
, Issue.1
, pp. 112-121
-
-
Goodeve, A.C.1
Eikenboom, J.2
Castaman, G.3
Rodeghiero, F.4
Federici, A.B.5
Batlle, J.6
Meyer, D.7
Mazurier, C.8
Goudemand, J.9
Schneppenheim, R.10
Budde, U.11
Ingerslev, J.12
Habart, D.13
Vorlova, Z.14
Holmberg, L.15
Lethagen, S.16
Pasi, J.17
Hill, F.18
Soteh, M.H.19
Baronciani, L.20
Hallden, C.21
Guilliatt, A.22
Lester, W.23
Peake, I.24
more..
-
10
-
-
44949188303
-
Distribution of von Willebrand factor levels in young women with and without bleeding symptoms. Influence of ABO blood group and promoter haplotypes
-
DOI 10.1160/TH07-06-0419
-
Lethagen S, Hillarp A, Ekholm C, Mattson E, Halldén C, Friberg B. Distribution of von Willebrand factor levels in young women with and without bleeding symptoms: influence of ABO blood group and promoter haplotypes. Thromb Haemost 2008 99 6 1013-1018 (Pubitemid 351810482)
-
(2008)
Thrombosis and Haemostasis
, vol.99
, Issue.6
, pp. 1013-1018
-
-
Lethagen, S.1
Hillarp, A.2
Ekholm, C.3
Mattson, E.4
Hallden, C.5
Friberg, B.6
-
11
-
-
0035159209
-
Von Willebrand factor does not vary during normal menstrual cycle
-
Onundarson PT, Gudmundsdottir BR, Arnfinnsdottir AV, Kjeld M, Olafsson O. von Willebrand factor does not vary during normal menstrual cycle. Thromb Haemost 2001 85 1 183-184 (Pubitemid 32050964)
-
(2001)
Thrombosis and Haemostasis
, vol.85
, Issue.1
, pp. 183-184
-
-
Onundarson, P.T.1
Gudmundsdottir, B.R.2
Arnfinnsdottir, A.V.3
Kjeld, M.4
Olafsson, O.5
-
12
-
-
23044515558
-
Provisional criteria for the diagnosis of VWD type 1
-
DOI 10.1111/j.1538-7836.2005.01245.x
-
Sadler JE, Rodeghiero F, ISTH SSC Subcommittee on von Willebrand Factor. Provisional criteria for the diagnosis of VWD type 1. J Thromb Haemost 2005 3 4 775-777 (Pubitemid 41647892)
-
(2005)
Journal of Thrombosis and Haemostasis
, vol.3
, Issue.4
, pp. 775-777
-
-
Sadler, J.E.1
Rodeghiero, F.2
-
13
-
-
33846433760
-
Risk of excessive bleeding associated with marginally low von Willebrand factor and mild platelet dysfunction
-
DOI 10.1111/j.1538-7836.2007.02326.x
-
Gudmundsdottir BR, Marder VJ, Onundarson PT. Risk of excessive bleeding associated with marginally low von Willebrand factor and mild platelet dysfunction. J Thromb Haemost 2007 5 2 274-281 (Pubitemid 46139451)
-
(2007)
Journal of Thrombosis and Haemostasis
, vol.5
, Issue.2
, pp. 274-281
-
-
Gudmundsdottir, B.R.1
Marder, V.J.2
Onundarson, P.T.3
-
14
-
-
33644979514
-
Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD
-
Eikenboom J, Van Marion V, Putter H et al. Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD. J Thromb Haemost 2006 4 4 774-782
-
(2006)
J Thromb Haemost
, vol.4
, Issue.4
, pp. 774-782
-
-
Eikenboom, J.1
Van Marion, V.2
Putter, H.3
-
15
-
-
77949445945
-
Low von Willebrand factor: Sometimes a risk factor and sometimes a disease
-
Sadler JE. Low von Willebrand factor: sometimes a risk factor and sometimes a disease. Hematology Am Soc Hematol Educ Program 2009 106-112
-
(2009)
Hematology Am Soc Hematol Educ Program
, pp. 106-112
-
-
Sadler, J.E.1
-
16
-
-
63149116476
-
Toward a new paradigm for the identification and functional characterization of von Willebrand disease
-
Favaloro EJ. Toward a new paradigm for the identification and functional characterization of von Willebrand disease. Semin Thromb Hemost 2009 35 1 60-75
-
(2009)
Semin Thromb Hemost
, vol.35
, Issue.1
, pp. 60-75
-
-
Favaloro, E.J.1
-
17
-
-
0027258360
-
Von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure
-
Holmberg L, Dent JA, Schneppenheim R, Budde U, Ware J, Ruggeri ZM. von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure. J Clin Invest 1993 91 5 2169-2177 (Pubitemid 23141493)
-
(1993)
Journal of Clinical Investigation
, vol.91
, Issue.5
, pp. 2169-2177
-
-
Holmberg, L.1
Dent, J.A.2
Schneppenheim, R.3
Budde, U.4
Ware, J.5
Ruggeri, Z.M.6
-
18
-
-
0033971892
-
Von Willebrand disease type 2M 'Vicenza' in Italian and German patients: Identification of the first candidate mutation (G3864A; R1205H) in 8 families
-
Schneppenheim R, Federici AB, Budde U et al. von Willebrand disease type 2M Vicenza in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 families. Thromb Haemost 2000 83 1 136-140 (Pubitemid 30045489)
-
(2000)
Thrombosis and Haemostasis
, vol.83
, Issue.1
, pp. 136-140
-
-
Schneppenheim, R.1
Federici, A.B.2
Budde, U.3
Castaman, G.4
Drewke, E.5
Krey, S.6
Mannucci, P.M.7
Riesen, G.8
Rodeghiero, F.9
Zieger, B.10
Zimmermann, R.11
-
19
-
-
0034912338
-
Type 2N von Willebrand disease: Clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology
-
DOI 10.1053/beha.2001.0138
-
Mazurier C, Goudemand J, Hilbert L, Caron C, Fressinaud E, Meyer D. Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology. Best Pract Res Clin Haematol 2001 14 2 337-347 (Pubitemid 32677083)
-
(2001)
Best Practice and Research in Clinical Haematology
, vol.14
, Issue.2
, pp. 337-347
-
-
Mazurier, C.1
Goudemand, J.2
Hilbert, L.3
Caron, C.4
Fressinaud, E.5
Meyer, D.6
-
20
-
-
34047271052
-
Identifying carriers of type 2N von Willebrand disease: Procedures and significance
-
DOI 10.1177/1076029606299000
-
Casonato A, Pontara E, Sartorello F et al. Identifying carriers of type 2N von Willebrand disease: procedures and significance. Clin Appl Thromb Hemost 2007 13 2 194-200 (Pubitemid 46548371)
-
(2007)
Clinical and Applied Thrombosis/Hemostasis
, vol.13
, Issue.2
, pp. 194-200
-
-
Casonato, A.1
Pontara, E.2
Sartorello, F.3
Cattini, M.G.4
Perutelli, P.5
Bertomoro, A.6
Gallinaro, L.7
Pagnan, A.8
-
21
-
-
0034912198
-
Congenital von Willebrand disease type 3: Clinical manifestations, pathophysiology and molecular biology
-
DOI 10.1053/beha.2001.0139
-
Eikenboom JC. Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology. Best Pract Res Clin Haematol 2001 14 2 365-379 (Pubitemid 32677085)
-
(2001)
Best Practice and Research in Clinical Haematology
, vol.14
, Issue.2
, pp. 365-379
-
-
Eikenboom, J.C.J.1
-
22
-
-
33748748642
-
Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: An international, multicenter study
-
DOI 10.1111/j.1538-7836.2006.02070.x
-
Castaman G, Rodeghiero F, Tosetto A et al. Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: an international, multicenter study. J Thromb Haemost 2006 4 10 2164-2169 (Pubitemid 44400291)
-
(2006)
Journal of Thrombosis and Haemostasis
, vol.4
, Issue.10
, pp. 2164-2169
-
-
Castaman, G.1
Rodeghiero, F.2
Tosetto, A.3
Cappelletti, A.4
Baudo, F.5
Eikenboom, J.C.J.6
Federici, A.B.7
Lethagen, S.8
Linari, S.9
Lusher, J.10
Nishino, M.11
Petrini, P.12
Srivastava, A.13
Ungerstedt, J.S.14
-
23
-
-
35748955202
-
Differential identification of a rare form of platelet-type (pseudo-) von Willebrand disease (VWD) from Type 2B VWD using a simplified ristocetin-induced-platelet-agglutination mixing assay and confirmed by genetic analysis [3]
-
DOI 10.1111/j.1365-2141.2007.06850.x
-
Favaloro EJ, Patterson D, Denholm A et al. Differential identification of a rare form of platelet-type (pseudo-) von Willebrand disease (VWD) from type 2B VWD using a simplified ristocetin-induced-platelet-agglutination mixing assay and confirmed by genetic analysis. Br J Haematol 2007 139 4 623-626 (Pubitemid 350043816)
-
(2007)
British Journal of Haematology
, vol.139
, Issue.4
, pp. 623-626
-
-
Favaloro, E.J.1
Patterson, D.2
Denholm, A.3
Mead, S.4
Gilbert, A.5
Collins, A.6
Estell, J.7
George, P.M.8
Smith, M.P.9
-
24
-
-
34247543029
-
Acquired von Willebrand syndrome: An update
-
DOI 10.1002/ajh.20830
-
Franchini M, Lippi G. Acquired von Willebrand syndrome: an update. Am J Hematol 2007 82 5 368-375 (Pubitemid 46651140)
-
(2007)
American Journal of Hematology
, vol.82
, Issue.5
, pp. 368-375
-
-
Franchini, M.1
Lippi, G.2
-
25
-
-
1242330853
-
Acquired von Willebrand syndrome 2004: International Registry. Diagnosis and management from online to bedside
-
Federici AB, Budde U, Rand JH. Acquired von Willebrand syndrome 2004: International Registrydiagnosis and management from online to bedside. Hamostaseologie 2004 24 1 50-55 (Pubitemid 38233047)
-
(2004)
Hamostaseologie
, vol.24
, Issue.1
, pp. 50-55
-
-
Federici, A.B.1
Budde, U.2
Rand, J.H.3
-
26
-
-
0023634567
-
Intranasal and intravenous administration of desmopressin: Effect on F VIII/vWF, pharmacokinetics and reproducibility
-
Lethagen S, Harris AS, Sjörin E, Nilsson IM. Intranasal and intravenous administration of desmopressin: effect on F VIII/vWF, pharmacokinetics and reproducibility. Thromb Haemost 1987 58 4 1033-1036
-
(1987)
Thromb Haemost
, vol.58
, Issue.4
, pp. 1033-1036
-
-
Lethagen, S.1
Harris, A.S.2
Sjörin, E.3
Nilsson, I.M.4
-
27
-
-
0027158362
-
Self-treatment with desmopressin intranasal spray in patients with bleeding disorders: Effect on bleeding symptoms and socioeconomic factors
-
Lethagen S, Ragnarson Tennvall G. Self-treatment with desmopressin intranasal spray in patients with bleeding disorders: effect on bleeding symptoms and socioeconomic factors. Ann Hematol 1993 66 5 257-260 (Pubitemid 23179050)
-
(1993)
Annals of Hematology
, vol.66
, Issue.5
, pp. 257-260
-
-
Lethagen, S.1
Tennvall, G.R.2
-
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 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 111 7 3531-3539
-
(2008)
Blood
, vol.111
, Issue.7
, pp. 3531-3539
-
-
Castaman, G.1
Lethagen, S.2
Federici, A.B.3
-
29
-
-
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 (Pubitemid 19198976)
-
(1989)
American Journal of Hematology
, vol.31
, Issue.3
, pp. 199-202
-
-
Smith, T.J.1
Gill, J.C.2
Ambruso, D.R.3
Hathaway, W.E.4
-
30
-
-
34250691461
-
Von Willebrand factor/factor VIII concentrate (Haemate P) dosing based on pharmacokinetics: A prospective multicenter trial in elective surgery
-
DOI 10.1111/j.1538-7836.2007.02588.x
-
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 (Pubitemid 46965370)
-
(2007)
Journal of Thrombosis and Haemostasis
, vol.5
, Issue.7
, pp. 1420-1430
-
-
Lethagen, S.1
Kyrle, P.A.2
Castaman, G.3
Haertel, S.4
Mannucci, P.M.5
Auerswald, G.6
Batlle, J.7
Castaman, G.8
Collins, P.9
D'Amico, E.10
Dasani, H.11
Federici, A.B.12
Hassenpflug, W.13
Heller, C.14
Hernandez-Navarro, F.15
Holmstrom, M.16
Ingerslev, J.17
Keeling, D.18
Klinge, J.19
Krause, M.20
Kreuz, W.21
Kyrle, P.A.22
Lopez Fernandez, F.23
Ludlam, C.A.24
Mannucci, P.M.25
Miesbach, W.26
Monteagudo, J.27
Muntean, E.W.28
Negrier, C.29
Petrini, P.30
Molina, M.Q.31
Ramschak, H.32
Reverter, J.-C.33
Scharrer, I.34
Schneppenheim, R.35
Schulman, S.36
Schved, J.F.37
Scognamiglio, F.38
Siebenhofer, A.39
Spranger, T.40
Tassies, D.41
Vallin, S.42
Camacho, A.V.43
Prondzinski, M.V.D.44
Weltermann, V.45
more..
-
31
-
-
0142240329
-
Gastrointestinal Bleeding, Angiodysplasia, Cardiovascular Disease, and Acquired von Willebrand Syndrome
-
DOI 10.1016/S0887-7963(03)00037-3
-
Warkentin TE, Moore JC, Anand SS, Lonn EM, Morgan DG. Gastrointestinal bleeding, angiodysplasia, cardiovascular disease, and acquired von Willebrand syndrome. Transfus Med Rev 2003 17 4 272-286 (Pubitemid 37310934)
-
(2003)
Transfusion Medicine Reviews
, vol.17
, Issue.4
, pp. 272-286
-
-
Warkentin, T.E.1
Moore, J.C.2
Anand, S.S.3
Lonn, E.M.4
Morgan, D.G.5
-
32
-
-
19944364505
-
Long-term prophylaxis in von Willebrand disease
-
Berntorp E, Petrini P. Long-term prophylaxis in von Willebrand disease. Blood Coagul Fibrinolysis 2005 16 Suppl 1 S23-S26 (Pubitemid 40756405)
-
(2005)
Blood Coagulation and Fibrinolysis
, vol.16
, Issue.SUPPL. 1
-
-
Berntorp, E.1
Petrini, P.2
-
33
-
-
58449095384
-
Use of recombinant factor VIIa in inherited and acquired von Willebrand disease
-
Sucker C, Scharf RE, Zotz RB. Use of recombinant factor VIIa in inherited and acquired von Willebrand disease. Clin Appl Thromb Hemost 2009 15 1 27-31
-
(2009)
Clin Appl Thromb Hemost
, vol.15
, Issue.1
, pp. 27-31
-
-
Sucker, C.1
Scharf, R.E.2
Zotz, R.B.3
|