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Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders

Journal of thrombosis and haemostasis, 2017-07, Vol.15 (7), p.1511-1521

2017

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Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patients

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.e201-e209

2012

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Peripartum bleeding management in a patient with CalDAG‐GEFI deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-11, Vol.23 (6), p.e533-e535

2017

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An acquired inhibitor to the GPVI platelet collagen receptor in a patient with lupus nephritis

Journal of thrombosis and haemostasis, 2009-09, Vol.7 (9), p.1541-1549

2009

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Use of autologous platelet-rich clots for the prevention of local injury bleeding in patients with severe inherited mucocutaneous bleeding disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-07, Vol.17 (4), p.620-624

2011

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Rare homozygous status of P43 β1-tubulin polymorphism causes alterations in platelet ultrastructure

Thrombosis and haemostasis, 2011-05, Vol.105 (5), p.855-863

2011

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Use of recombinant factor VIIa in 3 patients with inherited type I Glanzmann's thrombasthenia undergoing invasive procedures

Thrombosis and haemostasis, 2000-05, Vol.83 (5), p.644-647

2000

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Identification of the platelet ADP receptor targeted by antithrombotic drugs

Nature (London), 2001-01, Vol.409 (6817), p.202-207

2001

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Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

Haematologica (Roma), 2014-08, Vol.99 (8), p.1387-1394

2014

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Three cases of acquired von Willebrand disease associated with systemic lupus erythematosus

British journal of haematology, 1999-05, Vol.105 (2), p.532-537

1999

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Severe deficiency of glycoprotein VI in a patient with gray platelet syndrome

Blood, 2004-07, Vol.104 (1), p.107-114

2004

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Increased soluble and platelet-associated CD40 ligand in essential thrombocythemia and reactive thrombocytosis

Blood, 2002-04, Vol.99 (7), p.2612-2614

2002

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Decline in C-Reactive Protein After Successful Ablation of Long-Lasting Persistent Atrial Fibrillation

Journal of the American College of Cardiology, 2006-03, Vol.47 (6), p.1231-1233

2006

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Flow cytometry reveals activated GP IIb-IIIa complexes on platelets from patients undergoing thrombolytic therapy after acute myocardial infarction

Blood coagulation & fibrinolysis, 1995-07, Vol.6 (5), p.395-410

1995

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Platelet activation and thrombosis: Studies in a patient with essential thrombocythemia

American journal of hematology, 1996-01, Vol.51 (1), p.79-84

1996

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Screening for factor V Leiden and a prothrombin gene polymorphism in patients with Glanzmann's thrombasthenia

British journal of haematology, 1998-06, Vol.101 (3), p.593-594

1998

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Delayed immunologic thrombocytopenia induced by abciximab

Thrombosis and haemostasis, 2004-10, Vol.92 (4), p.820-828

2004

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Anti‐platelet antibodies in patients with systemic lupus erythematosus and the primary antiphospholipid antibody syndrome: their relationship with the observed thrombocytopenia

British journal of haematology, 1997-08, Vol.98 (2), p.336-341

1997

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Platelet ultrastructural abnormalities in three patients with type 2B von Willebrand disease

British journal of haematology, 2000-09, Vol.110 (3), p.704-714

2000

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Heterozygotes in the bernard–soulier syndrome do not necessarily have giant platelets or thrombocytopenia

British journal of haematology, 2003-02, Vol.120 (4), p.716-717

2003

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Epidural labor analgesia and parturient with type 2B von Willebrand disease

Annales françaises d'anesthésie et de réanimation, 2013-01, Vol.32 (1), p.56-59

2013

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PAICA: a method for characterizing platelet-associated antibodies--its application to the study of idiopathic thrombocytopenic purpura and to the detection of platelet-bound c7E3

Thrombosis and haemostasis, 1996, Vol.76 (6), p.1020-1029

1996

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Are patients with Glanzmann thrombasthenia and the Bernard-Soulier syndrome protected against atherosclerosis?

Advances in experimental medicine and biology, 2001, Vol.489, p.13

2001

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Two different beta3 cysteine substitutions alter alphaIIb beta3 maturation and result in Glanzmann thrombasthenia

Thrombosis and haemostasis, 2002-07, Vol.88 (1), p.104

2002

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Autoimmune thrombocytopenic purpura (AITP) and acquired thrombasthenia due to autoantibodies to GP IIb–IIIa in a patient with an unusual platelet membrane glycoprotein composition

American journal of hematology, 1998-02, Vol.57 (2), p.164-175

1998

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Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders

Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patients

Peripartum bleeding management in a patient with CalDAG‐GEFI deficiency

An acquired inhibitor to the GPVI platelet collagen receptor in a patient with lupus nephritis

Use of autologous platelet-rich clots for the prevention of local injury bleeding in patients with severe inherited mucocutaneous bleeding disorders

Rare homozygous status of P43 β1-tubulin polymorphism causes alterations in platelet ultrastructure

Use of recombinant factor VIIa in 3 patients with inherited type I Glanzmann's thrombasthenia undergoing invasive procedures

Identification of the platelet ADP receptor targeted by antithrombotic drugs

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

Three cases of acquired von Willebrand disease associated with systemic lupus erythematosus

Severe deficiency of glycoprotein VI in a patient with gray platelet syndrome

Increased soluble and platelet-associated CD40 ligand in essential thrombocythemia and reactive thrombocytosis

Decline in C-Reactive Protein After Successful Ablation of Long-Lasting Persistent Atrial Fibrillation

Flow cytometry reveals activated GP IIb-IIIa complexes on platelets from patients undergoing thrombolytic therapy after acute myocardial infarction

Platelet activation and thrombosis: Studies in a patient with essential thrombocythemia

Screening for factor V Leiden and a prothrombin gene polymorphism in patients with Glanzmann's thrombasthenia

Delayed immunologic thrombocytopenia induced by abciximab

Anti‐platelet antibodies in patients with systemic lupus erythematosus and the primary antiphospholipid antibody syndrome: their relationship with the observed thrombocytopenia

Platelet ultrastructural abnormalities in three patients with type 2B von Willebrand disease

Heterozygotes in the bernard–soulier syndrome do not necessarily have giant platelets or thrombocytopenia

Epidural labor analgesia and parturient with type 2B von Willebrand disease

PAICA: a method for characterizing platelet-associated antibodies--its application to the study of idiopathic thrombocytopenic purpura and to the detection of platelet-bound c7E3

Are patients with Glanzmann thrombasthenia and the Bernard-Soulier syndrome protected against atherosclerosis?

Two different beta3 cysteine substitutions alter alphaIIb beta3 maturation and result in Glanzmann thrombasthenia

Autoimmune thrombocytopenic purpura (AITP) and acquired thrombasthenia due to autoantibodies to GP IIb–IIIa in a patient with an unusual platelet membrane glycoprotein composition

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