-
2
-
-
66849141406
-
How I treat von Willebrand disease
-
Rodeghiero F, Castaman G, Tosetto A. How I treat von Willebrand disease. Blood 2009; 114: 1158-1165.
-
(2009)
Blood
, vol.114
, pp. 1158-1165
-
-
Rodeghiero, F.1
Castaman, G.2
Tosetto, A.3
-
3
-
-
33644977050
-
A quantitative analysys 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 analysys of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD). J Thromb Haemost 2006; 4: 766-773.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 766-773
-
-
Tosetto, A.1
Rodeghiero, F.2
Castaman, G.3
-
4
-
-
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: 526-534.
-
(2009)
Blood
, vol.113
, pp. 526-534
-
-
Federici, A.B.1
Mannucci, P.M.2
Castaman, G.3
-
5
-
-
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)
-
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: 112-121.
-
(2007)
Blood
, vol.109
, pp. 112-121
-
-
Goodeve, A.1
Eikenboom, J.2
Castaman, G.3
-
6
-
-
33846026307
-
The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study
-
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: 145-154.
-
(2007)
Blood
, vol.109
, pp. 145-154
-
-
James, P.D.1
Notley, C.2
Hegadorn, C.3
-
8
-
-
0015769115
-
von Willebrand's disease in Sweden
-
Silwer J. von Willebrand's disease in Sweden. Acta Paediatr. Scand Suppl 1973; 238: 1-159.
-
(1973)
Acta Paediatr Scand Suppl
, vol.238
, pp. 1-159
-
-
Silwer, J.1
-
9
-
-
11044235267
-
Clinical diagnosis of von Willebrand disease
-
Federici AB. Clinical diagnosis of von Willebrand disease. Haemophilia 2004; 10 (Suppl 4): 169-176.
-
(2004)
Haemophilia
, vol.10
, Issue.SUPPL. 4
, pp. 169-176
-
-
Federici, A.B.1
-
10
-
-
0034486136
-
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease
-
Lak M, Peyvandi F, Mannucci PM. Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease. Br J Haematol 2000; 111: 1236-1239.
-
(2000)
Br J Haematol
, vol.111
, pp. 1236-1239
-
-
Lak, M.1
Peyvandi, F.2
Mannucci, P.M.3
-
11
-
-
67849111584
-
Reduced von Willebrand factor survival in von Willebrand disease: Pathophysiologic and clinical relevance
-
Castaman G, Tosetto A, Rodeghiero F. Reduced von Willebrand factor survival in von Willebrand disease: pathophysiologic and clinical relevance. J Thomb Haemost 2009; 7 (Suppl 1): 71-74.
-
(2009)
J Thomb Haemost
, vol.7
, Issue.SUPPL. 1
, pp. 71-74
-
-
Castaman, G.1
Tosetto, A.2
Rodeghiero, F.3
-
12
-
-
1242338729
-
Increased clearance of von Willebrand factor antigen post-DDAVP in Type 1 von Willebrand disease: Is it a potential pathogenic process?
-
Brown SA, Eldridge A, Collins PW, et al. Increased clearance of von Willebrand factor antigen post-DDAVP in Type 1 von Willebrand disease: is it a potential pathogenic process? J Thromb Haemost 2003; 1: 1714-1717.
-
(2003)
J Thromb Haemost
, vol.1
, pp. 1714-1717
-
-
Brown, S.A.1
Eldridge, A.2
Collins, P.W.3
-
13
-
-
43949141204
-
Survival of von Willebrand factor released following DDAVP in a type 1 von Willebrand disease cohort: Influence of glycosylation, proteolysis and gene mutations
-
Millar CM, Riddell AF, Brown SA, et al. Survival of von Willebrand factor released following DDAVP in a type 1 von Willebrand disease cohort: influence of glycosylation, proteolysis and gene mutations. Thromb Haemost 2008; 99: 916-924.
-
(2008)
Thromb Haemost
, vol.99
, pp. 916-924
-
-
Millar, C.M.1
Riddell, A.F.2
Brown, S.A.3
-
14
-
-
33751013939
-
Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival
-
Haberichter SL, Balistreri M, Christopherson P, et al. Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival. Blood 2006; 108: 3344-3351.
-
(2006)
Blood
, vol.108
, pp. 3344-3351
-
-
Haberichter, S.L.1
Balistreri, M.2
Christopherson, P.3
-
15
-
-
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: 3531-3539.
-
(2008)
Blood
, vol.111
, pp. 3531-3539
-
-
Castaman, G.1
Lethagen, S.2
Federici, A.B.3
-
16
-
-
77956468012
-
Homozygous type 2 N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype
-
Castaman G, Giacomelli SH, Jacobi P, et al. Homozygous type 2 N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype. J Thromb Haemost 2010; 8: 2011-2016.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 2011-2016
-
-
Castaman, G.1
Giacomelli, S.H.2
Jacobi, P.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: 136-140.
-
(2000)
Thromb Haemost
, vol.83
, pp. 136-140
-
-
Schneppenheim, R.1
Federici, A.B.2
Budde, U.3
-
19
-
-
0023852791
-
von Willebrand disease "Vicenza" with larger-than-normal (supranormal) von Willebrand factor multimers
-
Mannucci PM, Lombardi R, Castaman G, et al. von Willebrand disease "Vicenza" with larger-than-normal (supranormal) von Willebrand factor multimers. Blood 1988; 71: 65-70.
-
(1988)
Blood
, vol.71
, pp. 65-70
-
-
Mannucci, P.M.1
Lombardi, R.2
Castaman, G.3
-
20
-
-
0036095699
-
Reduced von Willebrand factor survival in type Vicenza von Willebrand disease
-
Casonato A, Pontara E, Sartorello F, et al. Reduced von Willebrand factor survival in type Vicenza von Willebrand disease. Blood 2002; 99: 180-184.
-
(2002)
Blood
, vol.99
, pp. 180-184
-
-
Casonato, A.1
Pontara, E.2
Sartorello, F.3
-
21
-
-
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, et al. 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: 350-351.
-
(2000)
Thromb Haemost
, vol.84
, pp. 350-351
-
-
Castaman, G.1
Missiaglia, E.2
Federici, A.B.3
-
22
-
-
79955439988
-
Intersection of Mechanisms of Type 2A Von Willebrand Disease through Defects in Von Willebrand Factor Multimerization, Secretion, ADAMTS-13 Susceptibility, and Regulated Storage. ASH Annual Meeting Abstracts
-
Jacobi PM, Gill JC, Friedman KD, et al. Intersection of Mechanisms of Type 2A Von Willebrand Disease through Defects in Von Willebrand Factor Multimerization, Secretion, ADAMTS-13 Susceptibility, and Regulated Storage. ASH Annual Meeting Abstracts. Blood 2008; 112: 588.
-
(2008)
Blood
, vol.112
, pp. 588
-
-
Jacobi, P.M.1
Gill, J.C.2
Friedman, K.D.3
-
23
-
-
33748347075
-
Inherited and de novo von Willebrand disease Vicenza in UK families with the R1205H mutation: Diagnostic pitfalls and new insights
-
Lester WA, Guilliat AM, Surdhar GK, et al. Inherited and de novo von Willebrand disease Vicenza in UK families with the R1205H mutation: diagnostic pitfalls and new insights. Br J Haematol 2006; 135: 91-96.
-
(2006)
Br J Haematol
, vol.135
, pp. 91-96
-
-
Lester, W.A.1
Guilliat, A.M.2
Surdhar, G.K.3
-
24
-
-
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, et al. 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: 876-879.
-
(2000)
Br J Haematol
, vol.108
, pp. 876-879
-
-
Castaman, G.1
Eikenboom, J.C.J.2
Missiaglia, E.3
-
25
-
-
42149120672
-
Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)
-
Budde U, Schneppenheim R, Eikenboom J, et al. Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD). J Thromb Haemost 2008; 6: 762-771.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 762-771
-
-
Budde, U.1
Schneppenheim, R.2
Eikenboom, J.3
-
26
-
-
46749133213
-
Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: Molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD)
-
Haberichter SL, Castaman G, Budde U, et al. Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD). Blood 2008; 111: 4979-4985.
-
(2008)
Blood
, vol.111
, pp. 4979-4985
-
-
Haberichter, S.L.1
Castaman, G.2
Budde, U.3
-
27
-
-
29244439008
-
The discriminant power of bleeding history for the diagnosis of type 1 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 1 von Willebrand disease: an international, multicenter study. J Thromb Haemost 2005; 3: 2619-2626.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 2619-2626
-
-
Rodeghiero, F.1
Castaman, G.2
Tosetto, A.3
-
28
-
-
0036624746
-
The elusive pathogenesis of von Willebrand disease Vicenza
-
Castaman G, Rodeghiero F, Mannucci PM. The elusive pathogenesis of von Willebrand disease Vicenza. Blood 2002; 99: 4243-4244.
-
(2002)
Blood
, vol.99
, pp. 4243-4244
-
-
Castaman, G.1
Rodeghiero, F.2
Mannucci, P.M.3
-
29
-
-
28444499005
-
Cysteine-mutations in von Willebrand factor associated with increased clearance
-
Schooten CJ, Tjernberg P, Westein E, et al. Cysteine-mutations in von Willebrand factor associated with increased clearance. J Thromb Haemost 2005; 3: 2228-2237.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 2228-2237
-
-
Schooten, C.J.1
Tjernberg, P.2
Westein, E.3
-
30
-
-
0031892630
-
Pregnancy in women with von Willebrand's disease or factor XI deficiency
-
Kadir RA, Lee CA, Sabin CA, et al. Pregnancy in women with von Willebrand's disease or factor XI deficiency. Br J Obstet Gynaecol 1998; 105: 314-321.
-
(1998)
Br J Obstet Gynaecol
, vol.105
, pp. 314-321
-
-
Kadir, R.A.1
Lee, C.A.2
Sabin, C.A.3
-
31
-
-
33645559083
-
Factor VIII and von Willebrand factor changes after desmopressin and during pregnancy in type 2M von Willebrand disease Vicenza: A prospective study comparing patients with single (R1205H) and double (R1205H-M740I) defect
-
Castaman G, Federici AB, Bernardi M, et al. Factor VIII and von Willebrand factor changes after desmopressin and during pregnancy in type 2M von Willebrand disease Vicenza: a prospective study comparing patients with single (R1205H) and double (R1205H-M740I) defect. J Thromb Haemost 2006; 4: 357-360.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 357-360
-
-
Castaman, G.1
Federici, A.B.2
Bernardi, M.3
-
32
-
-
0033852254
-
Pregnancy in women with type 1 von Willebrand disease caused by heterozygosity for von Willebrand factor mutation C1130F
-
Castaman G, Eikenboom JCJ, Contri A, et al. Pregnancy in women with type 1 von Willebrand disease caused by heterozygosity for von Willebrand factor mutation C1130F. Thromb Haemost 2000; 84: 351-352.
-
(2000)
Thromb Haemost
, vol.84
, pp. 351-352
-
-
Castaman, G.1
Eikenboom, J.C.J.2
Contri, A.3
-
33
-
-
77953210923
-
Pregnancy and delivery in women with von Willebrand disease and different von Willebrand factor mutations
-
Castaman G, Tosetto A, Rodeghiero F. Pregnancy and delivery in women with von Willebrand disease and different von Willebrand factor mutations. Haematologica 2009; 95: 963-969.
-
(2009)
Haematologica
, vol.95
, pp. 963-969
-
-
Castaman, G.1
Tosetto, A.2
Rodeghiero, F.3
-
34
-
-
0026713114
-
Consistency of responses to repeated DDAVP infusions in patients with von Willebrand disease and haemophilia A
-
Mannucci PM, Bettega D, Cattaneo M. Consistency of responses to repeated DDAVP infusions in patients with von Willebrand disease and haemophilia A. Br J Haematol 1992; 82: 87-93.
-
(1992)
Br J Haematol
, vol.82
, pp. 87-93
-
-
Mannucci, P.M.1
Bettega, D.2
Cattaneo, M.3
|