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Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea.Academic Article Why?
Clinical and hematologic effects of hydroxyurea in children with sickle cell anemia.Academic Article Why?
Clinical relevance of vascular endothelial growth factor levels in sickle cell disease.Academic Article Why?
Exposure to hydroxyurea and pregnancy outcomes in patients with sickle cell anemia.Academic Article Why?
Fracture prevalence and relationship to endocrinopathy in iron overloaded patients with sickle cell disease and thalassemia.Academic Article Why?
Hemoglobin C disease.Academic Article Why?
Hydroxyurea and sickle cell anemia: effect on quality of life.Academic Article Why?
Medication adherence among pediatric patients with sickle cell disease: a systematic review.Academic Article Why?
N-terminal pro-brain natriuretic peptide levels and risk of death in sickle cell disease.Academic Article Why?
Parental and other factors associated with hydroxyurea use for pediatric sickle cell disease.Academic Article Why?
Platelet activation and inhibition in sickle cell disease (pains) study.Academic Article Why?
Quantitative magnetic resonance imaging analysis of the lacrimal gland in sickle cell disease.Academic Article Why?
Calpain-1 regulates platelet function in a humanized mouse model of sickle cell disease.Academic Article Why?
Lower hair cortisol among patients with sickle cell disease may indicate decreased adrenal reserves.Academic Article Why?
Quantitative Analysis of Extracranial Arterial Tortuosity in Patients with Sickle Cell Disease.Academic Article Why?
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