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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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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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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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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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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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Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high-molecular-weight multimers

The New England journal of medicine, 1982-02, Vol.306 (6), p.326-333

1982

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The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A-like phenotype of von Willebrand disease : study of 10 patients and mutated recombinant von Willebrand factor

Blood, 2001-02, Vol.97 (4), p.952-959

2001

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Total deficiency of specific von Willebrand factor-cleaving protease and recovery following plasma therapy in one patient with hemolytic-uremic syndrome

The hematology journal : the official journal of the European Haematology Association, 2001, Vol.2 (5), p.352-354

2001

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Heterogeneous abnormalities in the multimeric structure, antigenic properties, and plasma-platelet content of factor VIII/von Willebrand factor in subtypes of classic (type I) and variant (type IIA) von Willebrand's disease

The Journal of laboratory and clinical medicine, 1983-03, Vol.101 (3), p.411

1983

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Detection of Cutaneous Leishmaniasis Foci in South Ethiopia

The American journal of tropical medicine and hygiene, 2021-07, Vol.105 (1), p.156-158

2021

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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

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

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

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

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

Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high-molecular-weight multimers

The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A-like phenotype of von Willebrand disease : study of 10 patients and mutated recombinant von Willebrand factor

Prognostic value of anti-ADAMTS 13 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 ADAMTS 13 activity

Total deficiency of specific von Willebrand factor-cleaving protease and recovery following plasma therapy in one patient with hemolytic-uremic syndrome

Heterogeneous abnormalities in the multimeric structure, antigenic properties, and plasma-platelet content of factor VIII/von Willebrand factor in subtypes of classic (type I) and variant (type IIA) von Willebrand's disease

Detection of Cutaneous Leishmaniasis Foci in South Ethiopia

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