Marie J Stuart
Affiliation: Thomas Jefferson University
- Sickle-cell diseaseMarie J Stuart
Department of Pediatrics, Division of Hematology, the Marian Anderson Sickle Cell Anemia Research Hematology Laboratories, Thomas Jefferson University, Philadelphia, PA 19107, USA
Lancet 364:1343-60. 2004..Understanding of disease as the result of a continuing interaction between basic scientists and clinical researchers is best exemplified by this entity...
- Role of erythrocyte phosphatidylserine in sickle red cell-endothelial adhesionB N Yamaja Setty
Division of Research Hematology, Department of Pediatrics, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107, USA
Blood 99:1564-71. 2002..Our study signals the entrance of an important new contributor to the field of sickle erythrocyte-endothelial adhesion. The implications of erythrocyte PS exposure in relation to the vascular pathology of SCD need to be assessed...
- Eicosanoids in sickle cell disease: potential relevance of neutrophil leukotriene B4 to disease pathophysiologyB N Yamaja Setty
Marian Anderson Comprehensive Sickle Cell Anemia Care and Research Center, Department of Pediatrics, Division of Research Hematology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA
J Lab Clin Med 139:80-9. 2002..These properties of LTB(4) are relevant to disease pathophysiology, providing further evidence of the contribution of the neutrophil to the proinflammatory and proadhesive phenotype in SCD...
- Hypoxaemia in sickle cell disease: biomarker modulation and relevance to pathophysiologyB N Yamaja Setty
Department of Pediatrics and the Marian Anderson Sickle Cell Center Core Laboratory, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107, USA
Lancet 362:1450-5. 2003..We attempted to examine the biological relations, and describe the haematological risk factors for oxyhaemoglobin desaturation...