-
1
-
-
0034919227
-
Structure of von Willebrand factor and its function in platelet adhesion and thrombus formation
-
Ruggeri ZM. Structure of von Willebrand factor and its function in platelet adhesion and thrombus formation. Best Prac Res Clin Haematol 2001; 14: 257-79.
-
(2001)
Best Prac. Res. Clin. Haematol.
, vol.14
, pp. 257-279
-
-
Ruggeri, Z.M.1
-
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.
-
(2000)
Thromb. Haemost.
, vol.84
, pp. 160-174
-
-
Sadler, J.E.1
Mannucci, P.M.2
Berntorp, E.3
-
3
-
-
0036733501
-
Guidelines for diagnosis and treatment of von Willebrand disease in Italy
-
Federici AB, Castaman G, Mannucci PM. Guidelines for diagnosis and treatment of von Willebrand disease in Italy. Haemophilia 2002; 5: 607-21.
-
(2002)
Haemophilia
, vol.5
, pp. 607-621
-
-
Federici, A.B.1
Castaman, G.2
Mannucci, P.M.3
-
4
-
-
12244272130
-
Von Willebrand's disease in the year 2003: Toward the complete identification of gene defects for correct diagnosis and treatment
-
Castaman G, Federici AB, Rodeghiero F, Mannucci PM. von Willebrand's disease in the year 2003: toward the complete identification of gene defects for correct diagnosis and treatment. Haematologica 2003; 88: 94-108.
-
(2003)
Haematologica
, vol.88
, pp. 94-108
-
-
Castaman, G.1
Federici, A.B.2
Rodeghiero, F.3
Mannucci, P.M.4
-
5
-
-
11044230478
-
Mild forms of von Willebrand disease: Diagnosis and management
-
Federici AB. Mild forms of von Willebrand disease: diagnosis and management. Curr Hematol Rep 2003; 2: 373-80.
-
(2003)
Curr. Hematol. Rep.
, vol.2
, pp. 373-380
-
-
Federici, A.B.1
-
6
-
-
0028201807
-
A revised classification of von Willebrand disease
-
Sadler JE. A revised classification of von Willebrand disease. Thromb Haemost 1994; 71: 520-3.
-
(1994)
Thromb. Haemost.
, vol.71
, pp. 520-523
-
-
Sadler, J.E.1
-
7
-
-
12144289138
-
Biologic response to desmopressin in patients with severe types 1 and 2 von Willebrand Disease: Results of a multicenter prospective European study
-
Federici AB, Mazurier C, Bertorp E et al. Biologic response to desmopressin in patients with severe types 1 and 2 von Willebrand Disease: results of a multicenter prospective European study. Blood 2004; 103: 2032-8.
-
(2004)
Blood
, vol.103
, pp. 2032-2038
-
-
Federici, A.B.1
Mazurier, C.2
Bertorp, E.3
-
8
-
-
0037443406
-
Von Willebrand disease type 1: A diagnosis in search of a disease
-
Sadler JE. von Willebrand disease type 1: a diagnosis in search of a disease. Blood 2003; 101: 2089-93.
-
(2003)
Blood
, vol.101
, pp. 2089-2093
-
-
Sadler, J.E.1
-
9
-
-
0005579931
-
Acquired von Willebrand syndrome: Data from an International Registry
-
Federici AB, Rand JH, Bucciarelli P et al. Acquired von Willebrand syndrome: data from an International Registry. Thromb Haemost 2000; 84: 345-9.
-
(2000)
Thromb. Haemost.
, vol.84
, pp. 345-349
-
-
Federici, A.B.1
Rand, J.H.2
Bucciarelli, P.3
-
10
-
-
0025804299
-
Bleeding/bruising symptomatology in children with or without bleeding disorders
-
Nosek Cenkowska B, Cheang MS, Pizzi NJ et al. Bleeding/bruising symptomatology in children with or without bleeding disorders. Thromb Haemost 1991; 65: 237-41.
-
(1991)
Thromb. Haemost.
, vol.65
, pp. 237-241
-
-
Nosek Cenkowska, B.1
Cheang, M.S.2
Pizzi, N.J.3
-
11
-
-
0033828195
-
Von Willebrand disease in a pediatric-based population: Comparison of type 1 diagnostic criteria and use of the PFA-100 and von Willebrand factor: Collagen binding assays
-
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 von Willebrand factor: collagen binding assays. 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
-
-
0029065727
-
Usefulness of patient interview of bleeding disorders
-
Shramek A, Eikenboom JC, Briet E et al. Usefulness of patient interview of bleeding disorders. Arch Int Med 1995; 155 1409-15.
-
(1995)
Arch. Int. Med.
, vol.155
, pp. 1409-1415
-
-
Shramek, A.1
Eikenboom, J.C.2
Briet, E.3
-
13
-
-
11044238601
-
Clinical presentation of type 1 von Willebrand disease in obligatory carriers: Final results from a collaborative, international, multicentre study
-
OC078 Abstract
-
Castaman G, Tosetto A, Cappelletti A et al. Clinical presentation of type 1 von Willebrand disease in obligatory carriers: final results from a collaborative, international, multicentre study: J Thromb Haemost 2003; 1 (Suppl.): OC078 (Abstract).
-
(2003)
J. Thromb. Haemost.
, vol.1
, Issue.SUPPL.
-
-
Castaman, G.1
Tosetto, A.2
Cappelletti, A.3
-
14
-
-
0034912198
-
Congenital von Willebrand disease type 3: Clinical manifestations, pathophysiology and molecular biology
-
Eikemboom JC. Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology. Best Prac Res Clin Haematol 2001; 14: 365-79.
-
(2001)
Best Prac. Res. Clin. Haematol.
, vol.14
, pp. 365-379
-
-
Eikemboom, J.C.1
-
15
-
-
0037624499
-
Molecular defects in type 3 von Willebrand disease: Updated results from 40 multiethnic patients
-
Baronciani L, Cozzi G, Canciani MT et al. Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients. Blood Cells Molecules Dis 2003; 30: 264-70.
-
(2003)
Blood Cells Molecules Dis.
, vol.30
, pp. 264-270
-
-
Baronciani, L.1
Cozzi, G.2
Canciani, M.T.3
-
16
-
-
0034912429
-
Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function
-
Meyer D, Fressinaud E, Hilbert L et al. Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function. Best Prac Res Clin Haematol 2001; 14: 349-64.
-
(2001)
Best Prac. Res. Clin. Haematol.
, vol.14
, pp. 349-364
-
-
Meyer, D.1
Fressinaud, E.2
Hilbert, L.3
-
17
-
-
0026630044
-
Impaired cellular transport produced by a subset of type IIA von Willebrand disease mutations
-
Lyons SE, Bruck ME, Bowie EJW et al. Impaired cellular transport produced by a subset of type IIA von Willebrand disease mutations. J Biol Chem 1992; 267: 4424-30.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 4424-4430
-
-
Lyons, S.E.1
Bruck, M.E.2
Bowie, E.J.W.3
-
18
-
-
0033971892
-
Von Willebrand disease type 2 M '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 2 M 'Vicenza' in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 families. Thromb Haemost 2000; 83: 136-40.
-
(2000)
Thromb. Haemost.
, vol.83
, pp. 136-140
-
-
Schneppenheim, R.1
Federici, A.B.2
Budde, U.3
-
19
-
-
0033865397
-
An additional candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2M Vicenza and the G3864A (R1205H) mutation
-
Castaman G, Missiaglia E, Federici AB et al. An additional candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2M Vicenza and the G3864A (R1205H) mutation. Thromb Haemost 2000; 84: 350-1.
-
(2000)
Thromb. Haemost.
, vol.84
, pp. 350-351
-
-
Castaman, G.1
Missiaglia, E.2
Federici, A.B.3
-
20
-
-
0034912338
-
Type 2N von Willebrand disease: Clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology
-
Mazurier C, Goudemand J, Hilbert L et al. Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology. Best Prac Res Clin Haematol 2001; 14: 337-47.
-
(2001)
Best Prac. Res. Clin. Haematol.
, vol.14
, pp. 337-347
-
-
Mazurier, C.1
Goudemand, J.2
Hilbert, L.3
-
21
-
-
0034926029
-
Congenital von Willebrand disease type 1: Definition, phenotypes, clinical and laboratory assessment
-
Rodeghiero F, Castaman G. Congenital von Willebrand disease type 1: definition, phenotypes, clinical and laboratory assessment. Best Prac Res Clin Haematol 2001; 14: 321-35.
-
(2001)
Best Prac. Res. Clin. Haematol.
, vol.14
, pp. 321-335
-
-
Rodeghiero, F.1
Castaman, G.2
-
22
-
-
0029817840
-
Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor
-
Eikenboom JCJ, Matsushita T, Reitsma PH et al. Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor. Blood 1996; 88: 2433-41.
-
(1996)
Blood
, vol.88
, pp. 2433-2441
-
-
Eikenboom, J.C.J.1
Matsushita, T.2
Reitsma, P.H.3
-
23
-
-
0034030513
-
Autosomal dominant type 1 von Willebrand disease due to G3639T mutation (C1130F) in exon 26 of von Willebrand factor gene: Description of five Italian families and evidence for a founder effect
-
Castaman G, Eikenboom JCJ, Missiaglia E, Rodeghiero F. Autosomal dominant type 1 von Willebrand disease due to G3639T mutation (C1130F) in exon 26 of von Willebrand factor gene: description of five Italian families and evidence for a founder effect. Br J Haematol 2000; 108: 876-9.
-
(2000)
Br. J. Haematol.
, vol.108
, pp. 876-879
-
-
Castaman, G.1
Eikenboom, J.C.J.2
Missiaglia, E.3
Rodeghiero, F.4
-
24
-
-
0031957351
-
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin
-
Eikenboom JCJ, Castaman G, Vos H et al. Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin. Thromb Haemost 1998; 79: 709-17.
-
(1998)
Thromb. Haemost.
, vol.79
, pp. 709-717
-
-
Eikenboom, J.C.J.1
Castaman, G.2
Vos, H.3
-
25
-
-
0032823229
-
Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiologic investigation
-
Castaman G, Eikenboom JCJ, Bettina R, Rodeghiero F. Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiologic investigation. Thromb Haemost 1999; 82: 1065-70.
-
(1999)
Thromb. Haemost.
, vol.82
, pp. 1065-1070
-
-
Castaman, G.1
Eikenboom, J.C.J.2
Bettina, R.3
Rodeghiero, F.4
-
26
-
-
0033534406
-
MvWF, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase
-
Mohlke KL, Purkayastha AA, Westrick RJ et al. MvWF, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase. Cell 1999; 96: 111-20.
-
(1999)
Cell
, vol.96
, pp. 111-1120
-
-
Mohlke, K.L.1
Purkayastha, A.A.2
Westrick, R.J.3
-
27
-
-
0033137301
-
Low platelet α2β1 levels in type 1 von Willebrand disease correlate with impaired platelet function in a high shear stress system
-
Di Paola J, Federici AB, Mannucci PM et al. Low platelet α2β1 levels in type 1 von Willebrand disease correlate with impaired platelet function in a high shear stress system. Blood 1999; 93: 3578-82.
-
(1999)
Blood
, vol.93
, pp. 3578-3582
-
-
Di Paola, J.1
Federici, A.B.2
Mannucci, P.M.3
-
28
-
-
0015747575
-
Von Willebrand's disease in Sweden
-
Silwer J. von Willebrand's disease in Sweden. Acta Paediatr Scand 1973; 238: 1-159.
-
(1973)
Acta Paediatr. Scand.
, vol.238
, pp. 1-159
-
-
Silwer, J.1
-
29
-
-
0034486136
-
Clinical manifestations and complications of childbirth and replacement therapy in 348 Iranian patients with type 3 von Willebrand disease
-
Lak M, Peyvandi F, Mannucci PM. Clinical manifestations and complications of childbirth and replacement therapy in 348 Iranian patients with type 3 von Willebrand disease. Br J Haematol 2000; 111: 1223-9.
-
(2000)
Br. J. Haematol.
, vol.111
, pp. 1223-1229
-
-
Lak, M.1
Peyvandi, F.2
Mannucci, P.M.3
|