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Specific von Willebrand factor–cleaving protease in thrombotic microangiopathies: a study of 111 cases

Blood, 2001-09, Vol.98 (6), p.1765-1772

2001

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Thrombotic thrombocytopenic purpura related to severe ADAMTS13 deficiency in children

Pediatric nephrology (Berlin, West), 2009, Vol.24 (1), p.19-29

2009

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Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome)

Thrombosis and haemostasis, 2007-09, Vol.98 (3), p.593-599

2007

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Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF

Thrombosis and haemostasis, 1999-11, Vol.82 (5), p.1382-1385

1999

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Improvement of von Willebrand factor proteolysis after prostacyclin infusion in severe pulmonary arterial hypertension

Circulation (New York, N.Y.), 2000-11, Vol.102 (20), p.2460-2462

2000

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Comparison of FRETS-VWF73 to full-length VWF as a substrate for ADAMTS13 activity measurement in human plasma samples

Thrombosis and haemostasis, 2006-06, Vol.95 (6), p.1049-1051

2006

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A new mutation, S1285F, within the A1 loop of von Willebrand factor induces a conformational change in A1 loop with abnormal binding to platelet GPIb and botrocetin causing type 2M von Willebrand disease

British journal of haematology, 2003-02, Vol.120 (4), p.643-651

2003

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Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen

Thrombosis and haemostasis, 2001-09, Vol.86 (3), p.848-854

2001

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Complete defect in vWF-cleaving protease activity associated with increased shear-induced platelet aggregation in thrombotic microangiopathy

Thrombosis and haemostasis, 2002-05, Vol.87 (5), p.808-811

2002

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Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome

The Journal of pediatrics, 2003-03, Vol.142 (3), p.310-317

2003

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Assays of ADAMTS-13 activity

Seminars in hematology, 2004, Vol.41 (1), p.41-47

2004

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Mapping and functional studies of two alloantibodies developed in patients with type 3 von Willebrand disease

Thrombosis and haemostasis, 2000-02, Vol.83 (2), p.274-281

2000

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Thrombotic Thrombocytopenic Purpura Associated with von Willebrand Factor-Cleaving Protease (ADAMTS13) Deficiency in Children

Seminars in thrombosis and hemostasis, 2006-03, Vol.32 (2), p.090-097

2006

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New assay for measuring binding of platelet glycoprotein IIb/IIIa to unpurified von Willebrand factor

Thrombosis and haemostasis, 1999-07, Vol.82 (1), p.134-139

1999

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von Willebrand factor: structure and function

Thrombosis and haemostasis, 1993, Vol.70 (1), p.99-104

1993

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Von Willebrand factor C1C2 domain is involved in platelet adhesion to polymerized fibrin at high shear rate

Blood, 2004-03, Vol.103 (5), p.1741-1746

2004

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Conformational Changes in the A3 Domain of von Willebrand Factor Modulate the Interaction of the A1 Domain With Platelet Glycoprotein Ib

Blood, 1999-03, Vol.93 (6), p.1959-1968

1999

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Von Willebrand Factor: Structure and Function

Mayo Clinic proceedings, 1991-05, Vol.66 (5), p.516-523

1991

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Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease

Thrombosis and haemostasis, 2006-05, Vol.95 (5), p.776-781

2006

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Platelet aggregation induced by a monoclonal antibody to the A1 domain of von Willebrand factor

Blood, 1998-05, Vol.91 (10), p.3792-3799

1998

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Role of Platelet Membrane Glycoproteins and Von Willebrand Factor in Adhesion of Platelets to Subendothelium and Collagen

Annals of the New York Academy of Sciences, 1987-12, Vol.516 (1), p.52-65

1987

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Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)

Journal of thrombosis and haemostasis, 2004-03, Vol.2 (3), p.424-429

2004

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ADAMTS 13, la protéase spécifique du facteur von Willebrand

M.S. Médecine sciences, 2002-01, Vol.18 (1), p.15-17

2002

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Purpura thrombotique thrombocytopénique par déficit héréditaire en ADAMTS13 (syndrome d'Upshaw-Schulman) : actualités et perspectives

Hématologie, 2005-10, Vol.11 (5), p.321-324

2005

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Specific von Willebrand factor–cleaving protease in thrombotic microangiopathies: a study of 111 cases

Thrombotic thrombocytopenic purpura related to severe ADAMTS13 deficiency in children

Molecular characterization of four ADAMTS13 mutations responsible for congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome)

Prognostic value of anti-ADAMTS13 antibody features (Ig isotype, titer, and inhibitory effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic microangiopathy with undetectable ADAMTS13 activity

Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF

Improvement of von Willebrand factor proteolysis after prostacyclin infusion in severe pulmonary arterial hypertension

Comparison of FRETS-VWF73 to full-length VWF as a substrate for ADAMTS13 activity measurement in human plasma samples

A new mutation, S1285F, within the A1 loop of von Willebrand factor induces a conformational change in A1 loop with abnormal binding to platelet GPIb and botrocetin causing type 2M von Willebrand disease

Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen

Complete defect in vWF-cleaving protease activity associated with increased shear-induced platelet aggregation in thrombotic microangiopathy

Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome

Assays of ADAMTS-13 activity

Mapping and functional studies of two alloantibodies developed in patients with type 3 von Willebrand disease

Thrombotic Thrombocytopenic Purpura Associated with von Willebrand Factor-Cleaving Protease (ADAMTS13) Deficiency in Children

New assay for measuring binding of platelet glycoprotein IIb/IIIa to unpurified von Willebrand factor

von Willebrand factor: structure and function

Von Willebrand factor C1C2 domain is involved in platelet adhesion to polymerized fibrin at high shear rate

Conformational Changes in the A3 Domain of von Willebrand Factor Modulate the Interaction of the A1 Domain With Platelet Glycoprotein Ib

Von Willebrand Factor: Structure and Function

Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease

Platelet aggregation induced by a monoclonal antibody to the A1 domain of von Willebrand factor

Role of Platelet Membrane Glycoproteins and Von Willebrand Factor in Adhesion of Platelets to Subendothelium and Collagen

Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)

ADAMTS 13, la protéase spécifique du facteur von Willebrand

Purpura thrombotique thrombocytopénique par déficit héréditaire en ADAMTS13 (syndrome d'Upshaw-Schulman) : actualités et perspectives

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