Sickle cell anemia as an inflammatory disease

Journal of Clinical Investigation

Volumn 106, Issue 3, 2000, Pages 337-338

  Platt, O S ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN S; PADGEM PROTEIN;

BLOOD FLOW; ERYTHROCYTE MEMBRANE; HUMAN; INFLAMMATION; LEUKOCYTE ADHERENCE; LEUKOCYTE COUNT; NONHUMAN; NOTE; PATHOPHYSIOLOGY; PRIORITY JOURNAL; REPERFUSION INJURY; SICKLE CELL ANEMIA; VASCULAR ENDOTHELIUM;

EID: 0033837987     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI10726     Document Type: Note

References (9)

1. Hypoxia/reoxygenation causes inflammatory response in transgenic sickle mice but not in norreal mice
2. Blockade of adhesion of sickle cells to endothelium by monoclonal antibodies
3. Laboratory profile of sickle cell disease: A cross-sectional analysis. The Cooperative Study of Sickle Cell Disease
4. Pain in sickle cell disease. Rates and risk factors
5. Mortality in sickle cell disease. Life expectancy and risk factors for early death
6. The acute chest syndrome in sickle cell disease: Incidence and risk factors. The Cooperative Study of Sickle Cell Disease
7. Silent cerebral infarcts in sickle cell anemia: A risk factor analysis. The Cooperative Study of Sickle Cell Disease
8. Prediction of adverse outcomes in children with sickle cell disease
9. Genetic influences on F cells and other hematologic variables: A twin heritability study