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Ameliorating attention problems in children with sickle cell disease: a pilot study of methylphenidate.Academic Article Why?
Bidirectional processes linking social determinants of health and pediatric sickle cell anemia management: A qualitative study.Academic Article Why?
Calpain-1 regulates platelet function in a humanized mouse model of sickle cell disease.Academic Article Why?
Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea.Academic Article Why?
Characterizing medical decision-making in sickle cell disease during childhood: Qualitative perspectives of caregivers.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?
Effects of Experienced Discrimination in Pediatric Sickle Cell Disease: Caregiver and Provider Perspectives.Academic Article Why?
Executive Functioning Predicts Adaptive Functioning and Self-Care Independence in Pediatric 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?
Health-related quality of life in children with sickle cell disease using the child health questionnaire.Academic Article Why?
Hemoglobin C disease.Academic Article Why?
Hydroxyurea and sickle cell anemia: effect on quality of life.Academic Article Why?
Individuals with Sickle Cell Disease Using SBAR as a Communication Tool: A Pilot Study.Academic Article Why?
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