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Journal Articles

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

Yamaja Setty, PhD, Nigel S. Key, MBChB, Angara Koneti Rao, MD, Suba Krishnan, MD, Suhita Gayen-Betal, PhD, Marie J Stuart, MD

Blood (2010) 116 (21): 4210.

https://doi.org/10.1182/blood.V116.21.4210.4210

Published: 2010

Journal Articles

A Pilot Study of Tapered Oral Dexamethasone for the Acute Chest Syndrome of Sickle Cell Disease.

Charles T. Quinn, MD, MS, Marie J. Stuart, MD, Karen Kesler, PhD, Kenneth I. Ataga, MD, Winfred C. Wang, MD, Lori Styles, MD, Kim Smith-Whitley, MD, Ted Wun, MD, Suba Krishnan, MD, Frans A. Kuypers, PhD, Yamaja Setty, PhD, Nigel S. Key, MB, ChB, Seungshin Rhee, MS, George R. Buchanan, MD

Blood (2009) 114 (22): 1515.

https://doi.org/10.1182/blood.V114.22.1515.1515

Published: 2009

Journal Articles

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

Yamaja Setty, PhD, Suhita Gayen-Betal, PhD, Suba Krishnan, MD, Maureen Meier, RN, Michele Cahill, Marie J. Stuart, MD

Blood (2009) 114 (22): 2566.

https://doi.org/10.1182/blood.V114.22.2566.2566

Published: 2009

Journal Articles

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

Suhita Gayen Betal, Gregory J Kato, Marlene Peters Lawrence, Catherine Seamon, Yamaja Setty, PhD, Marie J. Stuart, MD, Suba Krishnan, MD

Blood (2009) 114 (22): 2587.

https://doi.org/10.1182/blood.V114.22.2587.2587

Published: 2009

Journal Articles

Phosphatidylserine (PS)-Positive Erythrocytes Bind to Both Immobilized and Soluble Thrombospondin-1 (TSP-1) Via Its Heparin Binding Domain.

Yamaja B.N. Setty, PhD, Suhita Gayen Betal, PhD, Surekha Kulkarni, BS, Marie J. Stuart, MD

Blood (2006) 108 (11): 1568.

https://doi.org/10.1182/blood.V108.11.1568.1568

Published: 2006

Journal Articles

Fetal Hemoglobin Protects Against Activation of Hemostasis Endothelial and Circulating Blood Cells in Sickle Cell Anemia.

Yamaja Setty, PhD, Vijender R. Vaidyula, PhD, Carlton D. Dampier, MD, A. Koneti Rao, MD, Marie J. Stuart, MD

Blood (2005) 106 (11): 3191.

https://doi.org/10.1182/blood.V106.11.3191.3191

Published: 2005

Journal Articles

Phosphatidylserine-Positive Erythrocytes Modulate Tissue Factor Activity In Vivo and In Vitro in Sickle Cell Disease.

Yamaja B.N Setty, Ph.D., Nigel S. Key, M.D., Marie J. Stuart, M.D.

Blood (2004) 104 (11): 240.

https://doi.org/10.1182/blood.V104.11.240.240

Published: 2004

Journal Articles

Role of erythrocyte phosphatidylserine in sickle red cell–endothelial adhesion

B. N. Yamaja Setty, Surekha Kulkarni, Marie J. Stuart

Blood (2002) 99 (5): 1564–1571.

https://doi.org/10.1182/blood.V99.5.1564

Published: 2002

Journal Articles

Thrombophilia in sickle cell disease: the red cell connection

B. N. Yamaja Setty, A. Koneti Rao, Marie J. Stuart

Blood (2001) 98 (12): 3228–3233.

https://doi.org/10.1182/blood.V98.12.3228

Published: 2001

Journal Articles

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

B. N. Yamaja Setty, Surekha Kulkarni, Carlton D. Dampier, Marie J. Stuart

Blood (2001) 97 (9): 2568–2573.

https://doi.org/10.1182/blood.V97.9.2568

Published: 2001

Journal Articles

Fetal hemoglobin in sickle cell disease: relationship to erythrocyte phosphatidylserine exposure and coagulation activation

B. N. Yamaja Setty, Surekha Kulkarni, A. Koneti Rao, Marie J. Stuart

Blood (2000) 96 (3): 1119–1124.

https://doi.org/10.1182/blood.V96.3.1119

Published: 2000

Journal Articles

Sickle Cell Acute Chest Syndrome: Pathogenesis and Rationale for Treatment

Marie J. Stuart, B.N. Yamaja Setty

Blood (1999) 94 (5): 1555–1560.

https://doi.org/10.1182/blood.V94.5.1555

Published: 1999

NARROW

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

A Pilot Study of Tapered Oral Dexamethasone for the Acute Chest Syndrome of Sickle Cell Disease.

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

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

Phosphatidylserine (PS)-Positive Erythrocytes Bind to Both Immobilized and Soluble Thrombospondin-1 (TSP-1) Via Its Heparin Binding Domain.

Fetal Hemoglobin Protects Against Activation of Hemostasis Endothelial and Circulating Blood Cells in Sickle Cell Anemia.

Phosphatidylserine-Positive Erythrocytes Modulate Tissue Factor Activity In Vivo and In Vitro in Sickle Cell Disease.

Role of erythrocyte phosphatidylserine in sickle red cell–endothelial adhesion

Thrombophilia in sickle cell disease: the red cell connection

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

Fetal hemoglobin in sickle cell disease: relationship to erythrocyte phosphatidylserine exposure and coagulation activation

Sickle Cell Acute Chest Syndrome: Pathogenesis and Rationale for Treatment

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ASH Publications

American Society of Hematology

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ASH Publications

American Society of Hematology

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