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Role of erythrocyte phosphatidylserine in sickle red cell–endothelial adhesion

Blood, 2002-03, Vol.99 (5), p.1564-1571

2002

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Microvascular endothelial cells express a phosphatidylserine receptor: a functionally active receptor for phosphatidylserine-positive erythrocytes

Blood, 2008-01, Vol.111 (2), p.905-914

2008

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Tissue factor-positive monocytes in children with sickle cell disease: correlation with biomarkers of haemolysis

British journal of haematology, 2012-05, Vol.157 (3), p.370-380

2012

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Hypoxaemia in sickle cell disease: biomarker modulation and relevance to pathophysiology

The Lancet (British edition), 2003-11, Vol.362 (9394), p.1450-1455

2003

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Thrombophilia in sickle cell disease: the red cell connection

Blood, 2001-12, Vol.98 (12), p.3228-3233

2001

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Specialized Pro-Resolving Mediator (SPM) Profile in Blood from Children with Sickle Cell Disease (SCD): Comparison with Age-, and Race- Matched Controls

Blood, 2022-11, Vol.140 (Supplement 1), p.11088-11088

2022

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Phosphatidylserine-positive erythrocytes bind to immobilized and soluble thrombospondin-1 via its heparin-binding domain

Translational research : the journal of laboratory and clinical medicine, 2008-10, Vol.152 (4), p.165-177

2008

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Pathophysiologic Implications of Type-2 Phosphatidylserine-Positive Erythrocytes in Hemoglobin SS Disease (sickle cell anemia) and β-Thalassemia

Blood, 2017-12, Vol.130, p.3521-3521

2017

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Tapered oral dexamethasone for the acute chest syndrome of sickle cell disease

British journal of haematology, 2011-10, Vol.155 (2), p.263-267

2011

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Fetal hemoglobin in sickle cell anemia: relationship to erythrocyte adhesion markers and adhesion

Blood, 2001-05, Vol.97 (9), p.2568-2573

2001

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Relationship of Omega-3 fatty acids DHA and EPA with the inflammatory biomarker hs-CRP in children with sickle cell anemia

Prostaglandins, leukotrienes and essential fatty acids, 2019-07, Vol.146, p.11-18

2019

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Type-2 Phosphatidylserine (PS)-Positive Erythrocytes and Their Association with Markers of Hemolysis and Hemostatic Activation in Children with Sickle Cell Disease (SCD)

Blood, 2015-12, Vol.126 (23), p.943-943

2015

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Increased levels of the inflammatory biomarker C‐reactive protein at baseline are associated with childhood sickle cell vasocclusive crises

British journal of haematology, 2010-03, Vol.148 (5), p.797-804

2010

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Quantitative Sensory Testing in Children with Sickle Cell Disease

Blood, 2017-12, Vol.130, p.3541-3541

2017

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Quantitative sensory testing in children with sickle cell disease: additional insights and future possibilities

British journal of haematology, 2019-06, Vol.185 (5), p.925-934

2019

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Microvascular Endothelial Cells Express Phosphatidylserine Receptor: A Functionally Active Receptor for Phosphatidylserine-Positive Erythrocytes

Blood, 2007-11, Vol.110 (11), p.1720-1720

2007

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Acute chest syndrome of sickle cell disease: new light on an old problem

Current opinion in hematology, 2001-03, Vol.8 (2), p.111-122

2001

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Tissue Factor Procoagulant Activity and Coagulation Activation In Sickle Cell Disease: Relationship with Biomarkers of Hemolysis and Inflammation

Blood, 2010-11, Vol.116 (21), p.4210-4210

2010

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Imbalance in Arachidonic Acid to Docosahexaenoic Acid Ratios in the Sickle Red Cell Is Associated with Inflammation

Blood, 2009-11, Vol.114 (22), p.2566-2566

2009

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Sickle cell vaso-occlusive crisis is associated with abnormalities in the ratio of vasoconstrictor to vasodilator prostanoids

Pediatric research, 1995-07, Vol.38 (1), p.95-102

1995

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Thrombin Generation in Sickle Cell Disease: Insights From Computerized Automated Thrombography

Blood, 2009-11, Vol.114 (22), p.2587-2587

2009

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Heme Induces Endothelial Tissue Factor Expression: Potential Role in Hemostatic Activation in Patients with Intravascular Hemolysis Including Sickle Cell Disease

Blood, 2008-11, Vol.112 (11), p.1902-1902

2008

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Inflammation and Coagulation Activation Influence Clinical Disease Burden in Sickle Cell Disease

Blood, 2008-11, Vol.112 (11), p.4812-4812

2008

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Sickle Cell Acute Chest Syndrome: Pathogenesis and Rationale for Treatment

Blood, 1999-09, Vol.94 (5), p.1555-1560

1999

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Sickle Cell Acute Chest Syndrome: Pathogenesis and Rationale for Treatment

Blood, 1999-09, Vol.94 (5), p.1555-1560

1999

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Role of erythrocyte phosphatidylserine in sickle red cell–endothelial adhesion

Microvascular endothelial cells express a phosphatidylserine receptor: a functionally active receptor for phosphatidylserine-positive erythrocytes

Tissue factor-positive monocytes in children with sickle cell disease: correlation with biomarkers of haemolysis

Hypoxaemia in sickle cell disease: biomarker modulation and relevance to pathophysiology

Thrombophilia in sickle cell disease: the red cell connection

Specialized Pro-Resolving Mediator (SPM) Profile in Blood from Children with Sickle Cell Disease (SCD): Comparison with Age-, and Race- Matched Controls

Phosphatidylserine-positive erythrocytes bind to immobilized and soluble thrombospondin-1 via its heparin-binding domain

Pathophysiologic Implications of Type-2 Phosphatidylserine-Positive Erythrocytes in Hemoglobin SS Disease (sickle cell anemia) and β-Thalassemia

Tapered oral dexamethasone for the acute chest syndrome of sickle cell disease

Fetal hemoglobin in sickle cell anemia: relationship to erythrocyte adhesion markers and adhesion

Relationship of Omega-3 fatty acids DHA and EPA with the inflammatory biomarker hs-CRP in children with sickle cell anemia

Type-2 Phosphatidylserine (PS)-Positive Erythrocytes and Their Association with Markers of Hemolysis and Hemostatic Activation in Children with Sickle Cell Disease (SCD)

Increased levels of the inflammatory biomarker C‐reactive protein at baseline are associated with childhood sickle cell vasocclusive crises

Quantitative Sensory Testing in Children with Sickle Cell Disease

Quantitative sensory testing in children with sickle cell disease: additional insights and future possibilities

Microvascular Endothelial Cells Express Phosphatidylserine Receptor: A Functionally Active Receptor for Phosphatidylserine-Positive Erythrocytes

Acute chest syndrome of sickle cell disease: new light on an old problem

Tissue Factor Procoagulant Activity and Coagulation Activation In Sickle Cell Disease: Relationship with Biomarkers of Hemolysis and Inflammation

Imbalance in Arachidonic Acid to Docosahexaenoic Acid Ratios in the Sickle Red Cell Is Associated with Inflammation

Sickle cell vaso-occlusive crisis is associated with abnormalities in the ratio of vasoconstrictor to vasodilator prostanoids

Thrombin Generation in Sickle Cell Disease: Insights From Computerized Automated Thrombography

Heme Induces Endothelial Tissue Factor Expression: Potential Role in Hemostatic Activation in Patients with Intravascular Hemolysis Including Sickle Cell Disease

Inflammation and Coagulation Activation Influence Clinical Disease Burden in Sickle Cell Disease

Sickle Cell Acute Chest Syndrome: Pathogenesis and Rationale for Treatment

Sickle Cell Acute Chest Syndrome: Pathogenesis and Rationale for Treatment

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