-
2
-
-
0032813139
-
The history of von Willebrand disease
-
Nilsson IM. The history of von Willebrand disease. Haemophilia 1999; 5(Suppl. 2): 7-11.
-
(1999)
Haemophilia
, vol.5
, Issue.SUPPL. 2
, pp. 7-11
-
-
Nilsson, I.M.1
-
3
-
-
84980100495
-
Über hereditäre Pseudohämaphilie
-
Von Willebrand EA. Über hereditäre Pseudohämaphilie. Acta Med Scand 1931; 67: 521-50.
-
(1931)
Acta Med Scand
, vol.67
, pp. 521-550
-
-
Von Willebrand, E.A.1
-
4
-
-
0001604165
-
Über ein vererbbares Blutungsübel: Die konstitutionelle Thrombopathie
-
Von Willebrand EA. Über ein vererbbares Blutungsübel: Die konstitutionelle Thrombopathie. Dtsch Arch Klin Med 1933; 175: 453-83.
-
(1933)
Dtsch Arch Klin Med
, vol.175
, pp. 453-483
-
-
Von Willebrand, E.A.1
-
5
-
-
77951395369
-
Willebrand-Jürgens syndrome and thrombopathies, study of 66 cases; attempt at classification
-
Soulier JP, Larrieu MJ. Willebrand-Jürgens syndrome and thrombopathies, study of 66 cases; attempt at classification. Rev Hematol 1954; 9: 77-122.
-
(1954)
Rev Hematol
, vol.9
, pp. 77-122
-
-
Soulier, J.P.1
Larrieu, M.J.2
-
6
-
-
77949430500
-
Optimizing treatment of von Willebrand disease by using phenotype and molecular data
-
January 1
-
Rodeghiero F, Castaman G, Tosetto A. Optimizing treatment of von Willebrand disease by using phenotype and molecular data. Hematology Am Soc Hematol Educ Program 2009; January 1: 113-23.
-
(2009)
Hematology Am Soc Hematol Educ Program
, pp. 113-123
-
-
Rodeghiero, F.1
Castaman, G.2
Tosetto, A.3
-
7
-
-
0019729424
-
Classification of variant von Willebrand's disease subtypes by analysis of functional characteristics and multimeric composition of factor VIII/von Willebrand factor
-
Ruggeri ZM, Zimmerman TS. Classification of variant von Willebrand's disease subtypes by analysis of functional characteristics and multimeric composition of factor VIII/von Willebrand factor. Ann N Y Acad Sci 1981; 370: 205-9.
-
(1981)
Ann N Y Acad Sci
, vol.370
, pp. 205-209
-
-
Ruggeri, Z.M.1
Zimmerman, T.S.2
-
8
-
-
0023612519
-
Von Willebrand factor and von Willebrand disease
-
Ruggeri ZM, Zimmerman TS. Von Willebrand factor and von Willebrand disease. Blood 1987; 70: 895-904.
-
(1987)
Blood
, vol.70
, pp. 895-904
-
-
Ruggeri, Z.M.1
Zimmerman, T.S.2
-
9
-
-
0028201807
-
A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
-
Sadler JE. A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 1994; 71: 520-5.
-
(1994)
Thromb Haemost
, vol.71
, pp. 520-525
-
-
Sadler, J.E.1
-
10
-
-
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 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.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 2103-2114
-
-
Sadler, J.E.1
Budde, U.2
Eikenboom, J.C.3
-
11
-
-
0026785327
-
Structures of the asparagine-linked oligosaccharide chains of human von Willebrand factor. Occurrence of blood group A, B, and H(O) structures
-
Matsui T, Titani K, Mizuochi T. Structures of the asparagine-linked oligosaccharide chains of human von Willebrand factor. Occurrence of blood group A, B, and H(O) structures. J Biol Chem 1992; 267: 8723-31.
-
(1992)
J Biol Chem
, vol.267
, pp. 8723-8731
-
-
Matsui, T.1
Titani, K.2
Mizuochi, T.3
-
12
-
-
0022457087
-
Amino acid sequence of human von Willebrand factor
-
Titani K, Kumar S, Takio K et al. Amino acid sequence of human von Willebrand factor. Biochemistry 1986; 25: 3171-84.
-
(1986)
Biochemistry
, vol.25
, pp. 3171-3184
-
-
Titani, K.1
Kumar, S.2
Takio, K.3
-
13
-
-
33645080188
-
Beyond lectins: the calnexin/calreticulin chaperone system of the endoplasmic reticulum
-
Williams DB. Beyond lectins: the calnexin/calreticulin chaperone system of the endoplasmic reticulum. J Cell Sci 2006; 119: 615-23.
-
(2006)
J Cell Sci
, vol.119
, pp. 615-623
-
-
Williams, D.B.1
-
14
-
-
0141707691
-
An influence of ABO blood group on the rate of proteolysis of von Willebrand factor by ADAMTS13
-
Bowen DJ. An influence of ABO blood group on the rate of proteolysis of von Willebrand factor by ADAMTS13. J Thromb Haemost 2003; 1: 33-40.
-
(2003)
J Thromb Haemost
, vol.1
, pp. 33-40
-
-
Bowen, D.J.1
-
15
-
-
77951017195
-
Expression of terminal alpha2-6-linked sialic acid on von Willebrand factor specifically enhances proteolysis by ADAMTS13
-
McGrath RT, McKinnon TA, Byrne B et al. Expression of terminal alpha2-6-linked sialic acid on von Willebrand factor specifically enhances proteolysis by ADAMTS13. Blood 2010; 115: 2666-73.
-
(2010)
Blood
, vol.115
, pp. 2666-2673
-
-
McGrath, R.T.1
McKinnon, T.A.2
Byrne, B.3
-
16
-
-
0025203450
-
The RIIIS/J inbred mouse strain as a model for von Willebrand disease
-
Sweeney JD, Novak EK, Reddington M, Takeuchi KH, Swank RT. The RIIIS/J inbred mouse strain as a model for von Willebrand disease. Blood 1990; 76: 2258-65.
-
(1990)
Blood
, vol.76
, pp. 2258-2265
-
-
Sweeney, J.D.1
Novak, E.K.2
Reddington, M.3
Takeuchi, K.H.4
Swank, R.T.5
-
17
-
-
77955499972
-
Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor
-
Flood VH, Gill JC, Morateck PA. et al. Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor. Blood 2010; 116: 280-6.
-
(2010)
Blood
, vol.116
, pp. 280-286
-
-
Flood, V.H.1
Gill, J.C.2
Morateck, P.A.3
-
18
-
-
2342625955
-
Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' 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: 218-31.
-
(2004)
Haemophilia
, vol.10
, pp. 218-231
-
-
Pasi, K.J.1
Collins, P.W.2
Keeling, D.M.3
-
19
-
-
66349136610
-
Evidence-based recommendations on the treatment of von Willebrand disease in Italy
-
Italian Association of Hemophilia Centers
-
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: 117-26.
-
(2009)
Blood Transfus
, vol.7
, pp. 117-126
-
-
Mannucci, P.M.1
Franchini, M.2
Castaman, G.3
Federici, A.B.4
-
20
-
-
77952581903
-
The genetic basis of von Willebrand disease
-
Goodeve AC. The genetic basis of von Willebrand disease. Blood Rev 2010; 24: 123-34.
-
(2010)
Blood Rev
, vol.24
, pp. 123-134
-
-
Goodeve, A.C.1
-
21
-
-
58149392261
-
Applying diagnostic criteria for type 1 von Willebrand disease to a pediatric population
-
Hyatt SA, Wang W, Kerlin BA, O'Brien SH. Applying diagnostic criteria for type 1 von Willebrand disease to a pediatric population. Pediatr Blood Cancer 2009; 52: 102-7.
-
(2009)
Pediatr Blood Cancer
, vol.52
, pp. 102-107
-
-
Hyatt, S.A.1
Wang, W.2
Kerlin, B.A.3
O'Brien, S.H.4
-
22
-
-
51349109299
-
Prophylaxis in von Willebrand disease
-
Berntorp E. Prophylaxis in von Willebrand disease. Haemophilia 2008; 14(Suppl. 5): 47-53.
-
(2008)
Haemophilia
, vol.14
, Issue.SUPPL. 5
, pp. 47-53
-
-
Berntorp, E.1
-
23
-
-
67649827227
-
Incidence of bleeding complications in pediatric patients with type 1 von Willebrand disease undergoing adenotonsillar procedures
-
Witmer CM, Elden L, Butler RB, Manno CS, Raffini LJ. Incidence of bleeding complications in pediatric patients with type 1 von Willebrand disease undergoing adenotonsillar procedures. J Pediatr 2009; 155: 68-72.
-
(2009)
J Pediatr
, vol.155
, pp. 68-72
-
-
Witmer, C.M.1
Elden, L.2
Butler, R.B.3
Manno, C.S.4
Raffini, L.J.5
-
24
-
-
79651469091
-
An infant with subdural haematoma and retinal haemorrhages: does von Willebrand disease explain the findings?
-
Stray-Pedersen A, Omland S, Nedregaard B, Klevberg S, Rognum TO. An infant with subdural haematoma and retinal haemorrhages: does von Willebrand disease explain the findings? Forensic Sci Med Pathol 2011; 7: 37-41.
-
(2011)
Forensic Sci Med Pathol
, vol.7
, pp. 37-41
-
-
Stray-Pedersen, A.1
Omland, S.2
Nedregaard, B.3
Klevberg, S.4
Rognum, T.O.5
-
25
-
-
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): S23-6.
-
(2005)
Blood Coagul Fibrinolysis
, vol.16
, Issue.SUPPL. 1
-
-
Berntorp, E.1
Petrini, P.2
-
26
-
-
77954858671
-
Clinical efficacy and safety of the factor VIII/von Willebrand factor concentrate BIOSTATE in patients with von Willebrand's disease: a prospective multi-centre study
-
Dunkley S, Baker RI, Pidcock M. et al. Clinical efficacy and safety of the factor VIII/von Willebrand factor concentrate BIOSTATE in patients with von Willebrand's disease: a prospective multi-centre study. Haemphilia 2010; 16: 615-24.
-
(2010)
Haemphilia
, vol.16
, pp. 615-624
-
-
Dunkley, S.1
Baker, R.I.2
Pidcock, M.3
-
27
-
-
63049123172
-
Treatment and prevention of acute bleedings in von Willebrand disease - efficacy and safety of Wilate, a new generation von Willebrand factor/factor VIII concentrate
-
European Wilate Study Group
-
Berntorp E, Windyga J; European Wilate Study Group. Treatment and prevention of acute bleedings in von Willebrand disease - efficacy and safety of Wilate, a new generation von Willebrand factor/factor VIII concentrate. Haemophilia 2009; 15: 122-30.
-
(2009)
Haemophilia
, vol.15
, pp. 122-130
-
-
Berntorp, E.1
Windyga, J.2
-
28
-
-
56649115781
-
Prophylaxis of bleeding episodes in patients with von Willebrand's disease
-
Federici AB. Prophylaxis of bleeding episodes in patients with von Willebrand's disease. Blood Transfus 2008; 6(Suppl. 2): S26-32.
-
(2008)
Blood Transfus
, vol.6
, Issue.SUPPL. 2
-
-
Federici, A.B.1
-
29
-
-
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. 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: 1115-24.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 1115-1124
-
-
Borel-Derlon, A.1
Federici, A.B.2
Roussel-Robert, V.3
-
30
-
-
84872213170
-
Personal communication
-
Berntorp E. Personal communication.
-
-
-
Berntorp, E.1
-
31
-
-
37249045532
-
Increasing life expectancy in Germany: quantitative contributions from changes in age- and disease-specific mortality
-
Klenk J, Rapp K, Büchele G, Keil U, Weiland SK. Increasing life expectancy in Germany: quantitative contributions from changes in age- and disease-specific mortality. Eur J Public Health 2007; 17: 587-92.
-
(2007)
Eur J Public Health
, vol.17
, pp. 587-592
-
-
Klenk, J.1
Rapp, K.2
Büchele, G.3
Keil, U.4
Weiland, S.K.5
-
32
-
-
0022002357
-
Life expectancy of Swedish haemophiliacs, 1831-1980
-
Larsson SA. Life expectancy of Swedish haemophiliacs, 1831-1980. Br J Haematol 1985; 59: 593-602.
-
(1985)
Br J Haematol
, vol.59
, pp. 593-602
-
-
Larsson, S.A.1
-
33
-
-
76149105503
-
Advances in hematology. Etiology and diagnosis of acquired von Willebrand syndrome
-
Franchini M, Lippi G, Favaloro EJ. Advances in hematology. Etiology and diagnosis of acquired von Willebrand syndrome. Clin Adv Hematol Oncol 2010; 8: 20-4.
-
(2010)
Clin Adv Hematol Oncol
, vol.8
, pp. 20-24
-
-
Franchini, M.1
Lippi, G.2
Favaloro, E.J.3
-
34
-
-
33644977050
-
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD)
-
Tosetto A, Rodgehiero 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
Rodgehiero, F.2
Castaman, G.3
-
35
-
-
34250696130
-
How to estimate bleeding risk in mild bleeding disorders
-
Rodeghiero F, Tosetto A, Castaman G. How to estimate bleeding risk in mild bleeding disorders. J Thromb Haemost 2007; 5(Suppl. 1): 157-66.
-
(2007)
J Thromb Haemost
, vol.5
, Issue.SUPPL. 1
, pp. 157-166
-
-
Rodeghiero, F.1
Tosetto, A.2
Castaman, G.3
-
37
-
-
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: 101-10.
-
(2010)
Haemophilia
, vol.16
, pp. 101-110
-
-
Federici, A.B.1
Barillari, G.2
Zanon, E.3
-
38
-
-
0036712293
-
Venous thromboembolism in von Willebrand disease
-
Mannucci PM. Venous thromboembolism in von Willebrand disease. Thromb Haemost 2002; 88: 378-9.
-
(2002)
Thromb Haemost
, vol.88
, pp. 378-379
-
-
Mannucci, P.M.1
-
39
-
-
0027079911
-
Pharmacokinetics and hemostatic effect of different factor VIII/von Willebrand factor concentrates in von Willebrand's disease type III
-
Lethagen S, Berntorp E, Nilsson IM. Pharmacokinetics and hemostatic effect of different factor VIII/von Willebrand factor concentrates in von Willebrand's disease type III. Ann Hematol 1992; 65: 253-9.
-
(1992)
Ann Hematol
, vol.65
, pp. 253-259
-
-
Lethagen, S.1
Berntorp, E.2
Nilsson, I.M.3
-
41
-
-
43149102964
-
Italian Registry of Haemophilia and Allied Disorders. Objectives, methodology and data analysis
-
Association of Italian Hemophilia Centres Directors
-
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: 444-53.
-
(2008)
Haemophilia
, vol.14
, pp. 444-453
-
-
Iorio, A.1
Oliovecchio, E.2
Morfini, M.3
Mannucci, P.M.4
-
42
-
-
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: 348-55.
-
(1995)
J Lab Clin Med
, vol.125
, pp. 348-355
-
-
Bergamaschini, L.1
Mannucci, P.M.2
Federici, A.B.3
Coppola, R.4
Guzzoni, S.5
Agostoni, A.6
-
43
-
-
2342656365
-
The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization
-
Laffan M, Brown SA, Collins PW. et al. The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization. Haemophilia 2004; 10: 199-217.
-
(2004)
Haemophilia
, vol.10
, pp. 199-217
-
-
Laffan, M.1
Brown, S.A.2
Collins, P.W.3
-
44
-
-
0033828195
-
von Willebrand disease in a pediatric-based population - comparison of type 1 diagnostic criteria and use of the PFA-100 and a von Wiillebrand factor/collagen binding assay
-
Dean JA, Blanchette VS, Carcao MD. et al. von Willebrand disease in a pediatric-based population - comparison of type 1 diagnostic criteria and use of the PFA-100 and a von Wiillebrand 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
-
45
-
-
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
-
46
-
-
81755171930
-
Nordic Haemophilia Council's practical guidelines on diagnosis and management of von Willebrand disease
-
Lassila R, Holme PA, Landorph A, Petrini P, Önundarson PT, Hillarp A. Nordic Haemophilia Council's practical guidelines on diagnosis and management of von Willebrand disease. Semin Thromb Haemost 2011; 37: 495-502.
-
(2011)
Semin Thromb Haemost
, vol.37
, pp. 495-502
-
-
Lassila, R.1
Holme, P.A.2
Landorph, A.3
Petrini, P.4
Önundarson, P.T.5
Hillarp, A.6
-
47
-
-
84872212427
-
-
Available at:.Accessed July 26, 2012.
-
Lethagen S, Ingerslev J, Holme PA, Petrini P, Lassila R, Önundarson PT. Nordic Guidelines for Diagnosis and Management of von Willebrand Disease. Guidelines of the Nordic Hemophilia Council. Available at: http://nordhaemophilia.org/document/NordicGuidelinesVWD_SL23APR2008b.pdf.Accessed July 26, 2012.
-
Nordic Guidelines for Diagnosis and Management of von Willebrand Disease. Guidelines of the Nordic Hemophilia Council
-
-
Lethagen, S.1
Ingerslev, J.2
Holme, P.A.3
Petrini, P.4
Lassila, R.5
Önundarson, P.T.6
-
48
-
-
83055187115
-
von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA)
-
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: 171-232.
-
(2008)
Haemophilia
, vol.14
, pp. 171-232
-
-
Nichols, W.L.1
Hultin, M.B.2
James, A.H.3
-
49
-
-
0032802763
-
von Willebrand disease: an update in the Åland islands. Summary of a Nordic symposium on von Willebrand disease, 24-25 September 1998, Mariehamn, Åland
-
Berntorp E, Ingerslev J, Schulman S. von Willebrand disease: an update in the Åland islands. Summary of a Nordic symposium on von Willebrand disease, 24-25 September 1998, Mariehamn, Åland. Haemophilia 1999; 6(Suppl. 2): 1-6.
-
(1999)
Haemophilia
, vol.6
, Issue.SUPPL. 2
, pp. 1-6
-
-
Berntorp, E.1
Ingerslev, J.2
Schulman, S.3
|