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Delayed hemolytic transfusion reaction in sickle cell diseaseUrinary albumin excretion is associated with pulmonary hypertension in sickle cell disease: potential role of soluble fms-like tyrosine kinase-1.Albuminuria Is Associated with Endothelial Dysfunction and Elevated Plasma Endothelin-1 in Sickle Cell Anemia.Beta-thalassaemia and sickle cell anaemia as paradigms of hypercoagulability.Coagulation abnormalities of sickle cell disease: Relationship with clinical outcomes and the effect of disease modifying therapies.Care seeking for pain in young adults with sickle cell disease.Hypercoagulability in sickle cell disease and beta-thalassemia.Hemostatic abnormalities in sickle cell disease.Pulmonary hypertension in sickle cell disease: diagnosis and management.Does hydroxyurea prevent pulmonary complications of sickle cell disease?Hypercoagulability and thrombotic complications in hemolytic anemias.Clinical Implications of the Association of Fetal Hemoglobin with Peripheral Oxygen Saturation in Sickle Cell Disease.Sickle Cardiomyopathy: The Missing Forest in the Trees.Monocytosis is associated with hemolysis in sickle cell disease.Prevalence of inherited blood disorders and associations with malaria and anemia in Malawian childrenRenal abnormalities in sickle cell diseaseRenal cell carcinomaMultiple myeloma in the breastMicroangiopathic hemolytic anemia associated with metastatic breast carcinomaThe acute chest syndrome of sickle cell diseaseLow hemoglobin increases risk for cerebrovascular disease, kidney disease, pulmonary vasculopathy, and mortality in sickle cell disease: A systematic literature review and meta-analysisRapid decline in estimated glomerular filtration rate is common in adults with sickle cell disease and associated with increased mortalityA pilot study of the effect of atorvastatin on endothelial function and albuminuria in sickle cell diseaseEffect of renin-angiotensin-aldosterone system blocking agents on progression of glomerulopathy in sickle cell diseaseUsing Machine Learning to Predict Early Onset Acute Organ Failure in Critically Ill Intensive Care Unit Patients With Sickle Cell Disease: Retrospective Study
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description
researcher
@en
wetenschapper
@nl
name
K I Ataga
@en
K I Ataga
@nl
type
label
K I Ataga
@en
K I Ataga
@nl
prefLabel
K I Ataga
@en
K I Ataga
@nl
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0000-0002-4501-9982