-
1
-
-
33748802581
-
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
-
JE Sadler, U Budde, JC Eikenboom, EJ Favaloro, FG Hill, L Holmberg 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 4 2006 2103 2114
-
(2006)
J Thromb Haemost
, vol.4
, pp. 2103-2114
-
-
Sadler, J.E.1
Budde, U.2
Eikenboom, J.C.3
Favaloro, E.J.4
Hill, F.G.5
Holmberg, L.6
-
2
-
-
78650513439
-
Identification and functional characterisation of von Willebrand Disease
-
EJ Favaloro Identification and functional characterisation of von Willebrand Disease US Hematology 2 1 2009 16 23
-
(2009)
US Hematology
, vol.2
, Issue.1
, pp. 16-23
-
-
Favaloro, E.J.1
-
3
-
-
63149116476
-
Towards a new paradigm for the identification and functional characterisation of von Willebrand disease
-
EJ Favaloro Towards a new paradigm for the identification and functional characterisation of von Willebrand disease Semin Thromb Hemost 35 2009 60 75
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 60-75
-
-
Favaloro, E.J.1
-
4
-
-
38549157588
-
An update on the von Willebrand factor collagen binding (VWF:CB) assay: 21 years of age and beyond adolescence, but not yet a mature adult
-
EJ Favaloro An update on the von Willebrand factor collagen binding (VWF:CB) assay: 21 years of age and beyond adolescence, but not yet a mature adult Semin Thromb Hemost 33 2007 727 744
-
(2007)
Semin Thromb Hemost
, vol.33
, pp. 727-744
-
-
Favaloro, E.J.1
-
5
-
-
78149472131
-
Genetic testing for the diagnosis of von Willebrand Disease: Benefits and limitations
-
EJ Favaloro, M Krigstein, J Koutts, T Brighton, R Lindeman Genetic testing for the diagnosis of von Willebrand Disease: benefits and limitations J Coag Disorders 2 2010 37 47
-
(2010)
J Coag Disorders
, vol.2
, pp. 37-47
-
-
Favaloro, E.J.1
Krigstein, M.2
Koutts, J.3
Brighton, T.4
Lindeman, R.5
-
6
-
-
73049110802
-
Genetic testing for von Willebrand disease: The case against
-
EJ Favaloro Genetic testing for von Willebrand disease: the case against J Thromb Haemost 8 2010 6 12
-
(2010)
J Thromb Haemost
, vol.8
, pp. 6-12
-
-
Favaloro, E.J.1
-
7
-
-
77956493323
-
ISTH/SSC bleeding assessment tool: A standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders
-
F Rodeghiero, A Tosetto, T Abshire, DM Arnold, B Coller, P James ISTH/SSC joint VWF and Perinatal/Pediatric Hemostasis Subcommittees Working Group ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders J Thromb Haemost 8 9 2010 Sep 2063 2065
-
(2010)
J Thromb Haemost
, vol.8
, Issue.9
, pp. 2063-2065
-
-
Rodeghiero, F.1
Tosetto, A.2
Abshire, T.3
Arnold, D.M.4
Coller, B.5
James, P.6
-
9
-
-
57149089069
-
Genetics of type 2B von Willebrand disease: "true 2B," "tricky 2B," or "not 2B." What are the modifiers of the phenotype?
-
M Othman, EJ Favaloro Genetics of type 2B von Willebrand disease: "true 2B," "tricky 2B," or "not 2B." What are the modifiers of the phenotype? Semin Thromb Hemost 34 2008 520 531
-
(2008)
Semin Thromb Hemost
, vol.34
, pp. 520-531
-
-
Othman, M.1
Favaloro, E.J.2
-
10
-
-
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
-
AB Federici, PM Mannucci, G Castaman, L Baronciani, P Bucciarelli, MT Canciani 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 113 3 2009 526 534
-
(2009)
Blood
, vol.113
, Issue.3
, pp. 526-534
-
-
Federici, A.B.1
Mannucci, P.M.2
Castaman, G.3
Baronciani, L.4
Bucciarelli, P.5
Canciani, M.T.6
-
11
-
-
0034852807
-
Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen
-
AS Ribba, I Loisel, JM Lavergne, I Juhan-Vague, B Obert, G Cherel Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen Thromb Haemost 86 3 2001 848 854
-
(2001)
Thromb Haemost
, vol.86
, Issue.3
, pp. 848-854
-
-
Ribba, A.S.1
Loisel, I.2
Lavergne, J.M.3
Juhan-Vague, I.4
Obert, B.5
Cherel, G.6
-
12
-
-
70350722434
-
Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factor
-
AF Riddell, K Gomez, CM Millar, G Mellars, S Gill, SA Brown Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factor Blood 114 16 2009 Oct 15 3489 3496
-
(2009)
Blood
, vol.114
, Issue.16
, pp. 3489-3496
-
-
Riddell, A.F.1
Gomez, K.2
Millar, C.M.3
Mellars, G.4
Gill, S.5
Brown, S.A.6
-
13
-
-
77954496769
-
Absent collagen binding in a VWF A3 domain mutant: Utility of the VWF:CB in diagnosis of VWD
-
VH Flood, CA Lederman, JS Wren, PA Christopherson, KD Friedman, RG Hoffmann Absent collagen binding in a VWF A3 domain mutant: utility of the VWF:CB in diagnosis of VWD J Thromb Haemost 8 2010 1431 1432
-
(2010)
J Thromb Haemost
, vol.8
, pp. 1431-1432
-
-
Flood, V.H.1
Lederman, C.A.2
Wren, J.S.3
Christopherson, P.A.4
Friedman, K.D.5
Hoffmann, R.G.6
-
14
-
-
70449584919
-
Identification and prevalence of von Willebrand Disease type 2N (Normandy) in Australia
-
EJ Favaloro, S Mohammed, J Koutts Identification and prevalence of von Willebrand Disease type 2N (Normandy) in Australia Blood Coag Fibrinolysis 20 2009 706 714
-
(2009)
Blood Coag Fibrinolysis
, vol.20
, pp. 706-714
-
-
Favaloro, E.J.1
Mohammed, S.2
Koutts, J.3
-
15
-
-
77949445945
-
Low von Willebrand factor: Sometimes a risk factor and sometimes a disease
-
JE Sadler Low von Willebrand factor: sometimes a risk factor and sometimes a disease Hematology Am Soc Hematol Educ Program 106-12 2009
-
(2009)
Hematology Am Soc Hematol Educ Program
, vol.106
, Issue.12
-
-
Sadler, J.E.1
-
16
-
-
0034545631
-
Assessment of current diagnostic practice and efficacy in testing for von Willebrand's disorder: Results from the second Australasian multi-laboratory survey
-
EJ Favaloro, J Thom, R Baker, on behalf of the Australasian Society for Thrombosis and Haemostasis (ASTH) Emerging Technologies Group Assessment of current diagnostic practice and efficacy in testing for von Willebrand's disorder: Results from the second Australasian multi-laboratory survey Blood Coag Fibrinolysis 11 2000 729 738
-
(2000)
Blood Coag Fibrinolysis
, vol.11
, pp. 729-738
-
-
Favaloro, E.J.1
Thom, J.2
Baker, R.3
-
17
-
-
63049088910
-
Lower limit of assay sensitivity: An under-recognised and significant problem in von Willebrand disease identification and classification
-
EJ Favaloro, R Bonar, K Marsden, on behalf of the RCPA QAP Haemostasis Committee Lower limit of assay sensitivity: an under-recognised and significant problem in von Willebrand disease identification and classification Clin Lab Sci 21 2008 178 185
-
(2008)
Clin Lab Sci
, vol.21
, pp. 178-185
-
-
Favaloro, E.J.1
Bonar, R.2
Marsden, K.3
-
18
-
-
58149099650
-
Preanalytical and postanalytical variables: The leading causes of diagnostic error in haemostasis?
-
EJ Favaloro, G Lippi, DM Adcock Preanalytical and postanalytical variables: The leading causes of diagnostic error in haemostasis? Semin Thromb Hemost 34 2008 612 634
-
(2008)
Semin Thromb Hemost
, vol.34
, pp. 612-634
-
-
Favaloro, E.J.1
Lippi, G.2
Adcock, D.M.3
-
19
-
-
34547890673
-
2B or not 2B? Disparate discrimination of functional VWF discordance using different assay panels or methodologies may lead to success or failure in the early identification of Type 2B VWD
-
EJ Favaloro, R Bonar, M Meiring, A Street, K Marsden, on behalf of the RCPA QAP in Haematology 2B or not 2B? Disparate discrimination of functional VWF discordance using different assay panels or methodologies may lead to success or failure in the early identification of Type 2B VWD Thromb Haemost 98 2007 346 358
-
(2007)
Thromb Haemost
, vol.98
, pp. 346-358
-
-
Favaloro, E.J.1
Bonar, R.2
Meiring, M.3
Street, A.4
Marsden, K.5
-
20
-
-
33746616053
-
Reducing errors in identification of von Willebrand disease: The experience of the Royal College of Pathologists of Australasia Quality Assurance Program
-
EJ Favaloro, R Bonar, G Kershaw, J Sioufi, R Baker, M Hertzberg on behalf of the RCPA QAP in Haematology Reducing errors in identification of von Willebrand disease: The experience of the Royal College of Pathologists of Australasia Quality Assurance Program Semin Thromb Hemost 32 2006 505 513
-
(2006)
Semin Thromb Hemost
, vol.32
, pp. 505-513
-
-
Favaloro, E.J.1
Bonar, R.2
Kershaw, G.3
Sioufi, J.4
Baker, R.5
Hertzberg, M.6
-
21
-
-
33746644201
-
An external quality assessment program for von Willebrand factor laboratory analysis: An overview from the European concerted action on thrombosis and disabilities foundation
-
P Meijer, F Haverkate An external quality assessment program for von Willebrand factor laboratory analysis: an overview from the European concerted action on thrombosis and disabilities foundation Semin Thromb Hemost 32 5 2006 485 491
-
(2006)
Semin Thromb Hemost
, vol.32
, Issue.5
, pp. 485-491
-
-
Meijer, P.1
Haverkate, F.2
-
22
-
-
54149117446
-
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) - A rebuttal
-
EJ Favaloro 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) - a rebuttal J Thromb Haemost 6 2008 1999 2001
-
(2008)
J Thromb Haemost
, vol.6
, pp. 1999-2001
-
-
Favaloro, E.J.1
-
23
-
-
63049090898
-
Desmopressin therapy to assist the functional identification and characterisation of von Willebrand disease: Differential utility from combining two (VWF:CB and VWF:RCo) von Willebrand factor activity assays?
-
EJ Favaloro, J Thom, D Patterson, S Just, T Dixon, J Koutts Desmopressin therapy to assist the functional identification and characterisation of von Willebrand disease: differential utility from combining two (VWF:CB and VWF:RCo) von Willebrand factor activity assays? Thromb Res 123 2009 862 868
-
(2009)
Thromb Res
, vol.123
, pp. 862-868
-
-
Favaloro, E.J.1
Thom, J.2
Patterson, D.3
Just, S.4
Dixon, T.5
Koutts, J.6
-
24
-
-
69549098342
-
Potential supplementary utility of combined PFA-100 and functional VWF testing for the laboratory assessment of desmopressin and factor concentrate therapy in von Willebrand disease
-
EJ Favaloro, J Thom, D Patterson, S Just, M Baccala, T Dixon Potential supplementary utility of combined PFA-100 and functional VWF testing for the laboratory assessment of desmopressin and factor concentrate therapy in von Willebrand disease Blood Coag Fibrinolysis 20 2009 475 483
-
(2009)
Blood Coag Fibrinolysis
, vol.20
, pp. 475-483
-
-
Favaloro, E.J.1
Thom, J.2
Patterson, D.3
Just, S.4
Baccala, M.5
Dixon, T.6
|