-
1
-
-
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..
-
2
-
-
34547889530
-
Management of inherited von Willebrand disease in 2007
-
DOI 10.1080/07853890701513738, PII 781252759
-
Federici AB, Mannucci PM. Management of inherited von Willebrand disease in 2007. Ann Med 2007 39 5 346-358 (Pubitemid 47262685)
-
(2007)
Annals of Medicine
, vol.39
, Issue.5
, pp. 346-358
-
-
Federici, A.B.1
Mannucci, P.M.2
-
3
-
-
0036733501
-
Guidelines for the diagnosis and management of VWD in Italy
-
Federici AB, Castaman G, Mannucci PM. Guidelines for the diagnosis and management of VWD in Italy. Haemophilia 2002 8 607-621
-
(2002)
Haemophilia
, vol.8
, pp. 607-621
-
-
Federici, A.B.1
Castaman, G.2
Mannucci, P.M.3
-
4
-
-
2342625955
-
Management of von Willebrand disease: A guideline from the UK Haemophilia Centre Doctor's Organization
-
Pasi KJ, Collins PW, Keeling DM et al. Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization. Haemophilia 2004 10 3 218-231 (Pubitemid 38584793)
-
(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
Hay, C.R.M.7
Hill, F.G.H.8
Laffan, M.9
Peake, I.R.10
-
5
-
-
83055187115
-
1
-
DOI 10.1111/j.1365-2516.2007.01643.x
-
Nichols WL, Hultin MB, James AH et al. von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA). Haemophilia 2008 14 2 171-232 (Pubitemid 351343618)
-
(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
Rick, M.E.7
Sadler, J.E.8
Weinstein, M.9
Yawn, B.P.10
-
6
-
-
66349136610
-
Evidence-based recommendations on the treatment of von Willebrand disease in Italy
-
Italian Association of Hemophilia Centers 2
-
Mannucci PM, Franchini M, Castaman G, Federici AB, Italian Association of Hemophilia Centers. Evidence-based recommendations on the treatment of von Willebrand disease in Italy. Blood Transfus 2009 7 2 117-126
-
(2009)
Blood Transfus
, vol.7
, pp. 117-126
-
-
Mannucci, P.M.1
Franchini, M.2
Castaman, G.3
Federici, A.B.4
-
7
-
-
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
-
8
-
-
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 2 454-459 (Pubitemid 17022013)
-
(1987)
Blood
, vol.69
, Issue.2
, pp. 454-459
-
-
Rodeghiero, F.1
Castaman, G.2
Dini, E.3
-
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
-
-
33846026307
-
The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study
-
DOI 10.1182/blood-2006-05-021105.
-
James PD, Notley C, Hegadorn C et al. The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study. Blood 2007 109 1 145-154 (Pubitemid 46053055)
-
(2007)
Blood
, vol.109
, Issue.1
, pp. 145-154
-
-
James, P.D.1
Notley, C.2
Hegadorn, C.3
Leggo, J.4
Tuttle, A.5
Tinlin, S.6
Brown, C.7
Andrews, C.8
Labelle, A.9
Chirinian, Y.10
O'Brien, L.11
Othman, M.12
Rivard, G.13
Rapson, D.14
Hough, C.15
Lillicrap, D.16
-
11
-
-
0017334854
-
Spectrum of von Willebrand's disease: A study of 100 cases
-
Barbui T, Baudo F, Ciavarella N et al, Italian Working Group. Spectrum of von Willebrand's disease: a study of 100 cases. Br J Haematol 1977 35 1 101-112 (Pubitemid 8031351)
-
(1977)
British Journal of Haematology
, vol.35
, Issue.1
, pp. 101-112
-
-
Barbui, T.1
Baudo, F.2
Ciavarella, N.3
-
12
-
-
0017336844
-
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-d-arginine vasopressin: a new pharmacological approach to the management of haemophilia and von Willebrands' diseases. Lancet 1977 1 8017 869-872 (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
-
13
-
-
43149102964
-
Italian Registry of Haemophilia and Allied Disorders. Objectives, methodology and data analysis
-
DOI 10.1111/j.1365-2516.2008.01679.x
-
Iorio A, Oliovecchio E, Morfini M, Mannucci PM, Association of Italian Hemophilia Centres Directors. Italian Registry of Haemophilia and Allied Disorders. Objectives, methodology and data analysis. Haemophilia 2008 14 3 444-453 (Pubitemid 351638730)
-
(2008)
Haemophilia
, vol.14
, Issue.3
, pp. 444-453
-
-
Iorio, A.1
Oliovecchio, E.2
Morfini, M.3
Mannucci, P.M.4
-
14
-
-
0842307008
-
A sensitive ristocetin co-factor activity assay with recombinant glycoprotein Ibα for the diagnosis of patients with low von Willebrand factor levels
-
Federici AB, Canciani MT, Forza I et al. A sensitive ristocetin co-factor activity assay with recombinant glycoprotein Ibalpha for the diagnosis of patients with low von Willebrand factor levels. Haematologica 2004 89 1 77-85 (Pubitemid 38165858)
-
(2004)
Haematologica
, vol.89
, Issue.1
, pp. 77-85
-
-
Federici, A.B.1
Canciani, M.T.2
Forza, I.3
Mannucci, P.M.4
Marchese, P.5
Ware, J.6
Ruggeri, Z.M.7
-
15
-
-
0033782679
-
Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease
-
Baronciani L, Cozzi G, Canciani MT 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
-
16
-
-
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
-
17
-
-
66049121391
-
Clinical and laboratory versus molecular markers for a correct classification of von Willebrand disease
-
Federici AB, Canciani MT. Clinical and laboratory versus molecular markers for a correct classification of von Willebrand disease. Haematologica 2009 94 5 610-615
-
(2009)
Haematologica
, vol.94
, Issue.5
, pp. 610-615
-
-
Federici, A.B.1
Canciani, M.T.2
-
18
-
-
12144289138
-
Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: Results of a multicenter European study
-
DOI 10.1182/blood-2003-06-2072
-
Federici AB, Mazurier C, Berntorp E 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 103 6 2032-2038 (Pubitemid 38326217)
-
(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
Lethagen, S.7
Nitu, I.8
Ludwig, G.9
Hilbert, L.10
Mannucci, P.M.11
-
19
-
-
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
-
20
-
-
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
-
21
-
-
34548364967
-
" P in inherited von Willebrand's disease: A cohort study on 100 Italian patients
-
DOI 10.3324/haematol.11124
-
Federici AB, Castaman G, Franchini M et al. Clinical use of Haemate P in inherited von Willebrand's disease: a cohort study on 100 Italian patients. Haematologica 2007 92 7 944-951 (Pubitemid 350144241)
-
(2007)
Haematologica
, vol.92
, Issue.7
, pp. 944-951
-
-
Federici, A.B.1
Castaman, G.2
Franchini, M.3
Morfini, M.4
Zanon, E.5
Coppola, A.6
Tagliaferri, A.7
Boeri, E.8
Mazzucconi, M.G.9
Rossetti, G.10
Mannucci, P.M.11
-
22
-
-
73949148650
-
Efficacy and safety of highly purified, doubly virus-inactivated VWF/FVIII concentrates in inherited von Willebrand's disease: Results of an Italian cohort study on 120 patients characterized by bleeding severity score
-
Federici AB, Barillari G, Zanon E et al. Efficacy and safety of highly purified, doubly virus-inactivated VWF/FVIII concentrates in inherited von Willebrand's disease: results of an Italian cohort study on 120 patients characterized by bleeding severity score. Haemophilia 2010 16 1 101-110
-
(2010)
Haemophilia
, vol.16
, Issue.1
, pp. 101-110
-
-
Federici, A.B.1
Barillari, G.2
Zanon, E.3
-
23
-
-
37149005797
-
Highly purified VWF/FVIII concentrates in the treatment and prophylaxis of von Willebrand disease: The PRO.WILL Study
-
DOI 10.1111/j.1365-2516.2007.01573.x
-
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 (Pubitemid 350253400)
-
(2007)
Haemophilia
, vol.13
, Issue.SUPPL. 5
, pp. 15-24
-
-
Federici, A.B.1
-
24
-
-
0034532364
-
Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients: A reappraisal using phenotypes, genotypes and molecular modelling
-
Nitu-Whalley IC, Riddell A, Lee CA et al. Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients: a reappraisal using phenotypes, genotypes and molecular modelling. Thromb Haemost 2000 84 6 998-1004 (Pubitemid 32014035)
-
(2000)
Thrombosis and Haemostasis
, vol.84
, Issue.6
, pp. 998-1004
-
-
Nitu-Whalley, I.C.1
Riddell, A.2
Lee, C.A.3
Pasi, K.J.4
Owens, D.5
Enayat, M.S.6
Perkins, S.J.7
Jenkins, P.V.8
-
25
-
-
12344262502
-
Phenotypic and genotypic diagnosis of von Willebrand disease: A 2004 update
-
DOI 10.1053/j.seminhematol.2004.10.002, PII S0037196304002501, von Willebrand Factor in Hemostasis and Thrombosis
-
Schneppenheim R, Budde U. Phenotypic and genotypic diagnosis of von Willebrand disease: a 2004 update. Semin Hematol 2005 42 1 15-28 (Pubitemid 40127266)
-
(2005)
Seminars in Hematology
, vol.42
, Issue.1
, pp. 15-28
-
-
Schneppenheim, R.1
Budde, U.2
-
26
-
-
0033985083
-
Collagen binding assay for von Willebrand factor (VWF:CBA): Detection of von Willebrands disease (VWD), and discrimination of VWD subtypes, depends on collagen source
-
Favaloro EJ. Collagen binding assay for von Willebrand factor (VWF:CBA): detection of von Willebrands disease (VWD), and discrimination of VWD subtypes, depends on collagen source. Thromb Haemost 2000 83 1 127-135 (Pubitemid 30045488)
-
(2000)
Thrombosis and Haemostasis
, vol.83
, Issue.1
, pp. 127-135
-
-
Favaloro, E.J.1
-
27
-
-
0034537373
-
Ristocetin cofactor and collagen binding activities normalized to antigen levels for a rapid diagnosis of type 2 von Willebrand disease: Single center comparison of four different assays
-
Federici AB, Canciani MT, Forza I, Cozzi G. Ristocetin cofactor and collagen binding activities normalized to antigen levels for a rapid diagnosis of type 2 von Willebrand diseasesingle center comparison of four different assays. Thromb Haemost 2000 84 6 1127-1128 (Pubitemid 32014059)
-
(2000)
Thrombosis and Haemostasis
, vol.84
, Issue.6
, pp. 1127-1128
-
-
Federici, A.B.1
Canciani, M.T.2
Forza, I.3
Cozzi, G.4
-
28
-
-
78149491049
-
Evaluation of commercial von Willebrand factor collagen binding assays to assist the discrimination of types 1 and 2 von Willebrand disease
-
Favaloro EJ. Evaluation of commercial von Willebrand factor collagen binding assays to assist the discrimination of types 1 and 2 von Willebrand disease. Thromb Haemost 2010 104 5 1009-1021
-
(2010)
Thromb Haemost
, vol.104
, Issue.5
, pp. 1009-1021
-
-
Favaloro, E.J.1
-
29
-
-
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 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 3 526-534
-
(2009)
Blood
, vol.113
, Issue.3
, pp. 526-534
-
-
Federici, A.B.1
Mannucci, P.M.2
Castaman, G.3
-
30
-
-
0023237159
-
Gene deletions correlate with the development of alloantibodies in von Willebrand disease
-
Shelton-Inloes BB, Chehab FF, Mannucci PM, 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
-
31
-
-
0023469711
-
Life-threatening 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 et al. Life-threatening reaction to factor VIII concentrate in a patient with severe von Willebrand disease and alloantibodies to von Willebrand factor. Eur J Haematol 1987 39 5 467-470 (Pubitemid 18002930)
-
(1987)
European Journal of Haematology
, 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
Tedesco, F.7
-
32
-
-
0029267038
-
Posttransfusion anaphylactic reactions in a patient with severe von Willebrand disease: Role of complement and alloantibodies to von Willebrand factor
-
Bergamaschini L, Mannucci PM, Federici AB, Coppola R, Guzzoni S, Agostoni A. Posttransfusion anaphylactic reactions in a patient with severe von Willebrand disease: role of complement and alloantibodies to von Willebrand factor. J Lab Clin Med 1995 125 3 348-355
-
(1995)
J Lab Clin Med
, vol.125
, Issue.3
, pp. 348-355
-
-
Bergamaschini, L.1
Mannucci, P.M.2
Federici, A.B.3
Coppola, R.4
Guzzoni, S.5
Agostoni, A.6
-
33
-
-
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
-
34
-
-
0033865397
-
An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and the G3864A (R1205H) mutation
-
Castaman G, Missiaglia E, Federici AB, Schneppenheim R, Rodeghiero F. An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and the G3864A (R1205H) mutation. Thromb Haemost 2000 84 2 350-351 (Pubitemid 30601486)
-
(2000)
Thrombosis and Haemostasis
, vol.84
, Issue.2
, pp. 350-351
-
-
Castaman, G.1
Missiaglia, E.2
Federici, A.B.3
Schneppenheim, R.4
Rodeghiero, F.5
-
35
-
-
52449098463
-
Clinical and molecular markers of inherited von Willebrand disease type 3: Are deletions of the VWF gene associated with alloantibodies to VWF
-
Federici AB. Clinical and molecular markers of inherited von Willebrand disease type 3: are deletions of the VWF gene associated with alloantibodies to VWF? J Thromb Haemost 2008 6 10 1726-1728
-
(2008)
J Thromb Haemost
, vol.6
, Issue.10
, pp. 1726-1728
-
-
Federici, A.B.1
-
36
-
-
37449014098
-
The use of desmopressin in von Willebrand disease: The experience of the first 30 years (19772007)
-
Federici AB. The use of desmopressin in von Willebrand disease: the experience of the first 30 years (19772007). Haemophilia 2008 14 Suppl 1 5-14
-
(2008)
Haemophilia
, vol.14
, Issue.SUPPL. 1
, pp. 5-14
-
-
Federici, A.B.1
-
37
-
-
33645961294
-
The natural history of hepatitis C virus infection in Italian patients with von Willebrand's disease: A cohort study
-
Federici AB, Santagostino E, Rumi MG et al. The natural history of hepatitis C virus infection in Italian patients with von Willebrand's disease: a cohort study. Haematologica 2006 91 4 503-508
-
(2006)
Haematologica
, vol.91
, Issue.4
, pp. 503-508
-
-
Federici, A.B.1
Santagostino, E.2
Rumi, M.G.3
|