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One or more keywords matched the following items that are connected to Platt, Orah
Item TypeName
Academic Article Acquisition of mutans streptococci and caries prevalence in pediatric sickle cell anemia patients receiving long-term antibiotic therapy.
Academic Article Oral magnesium supplements reduce erythrocyte dehydration in patients with sickle cell disease.
Academic Article Reticulocyte hemoglobin: an integrated parameter for evaluation of erythropoietic activity.
Academic Article Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group.
Academic Article The febrile child with sickle cell disease: a pediatrician's quandary.
Academic Article Hydroxyurea for the treatment of sickle cell anemia.
Academic Article Pathology of membrane proteins in sickle erythrocytes.
Academic Article Influence of sickle hemoglobinopathies on growth and development.
Academic Article Molecular defect in the sickle erythrocyte skeleton. Abnormal spectrin binding to sickle inside-our vesicles.
Academic Article Sickle reticulocytes adhere to VCAM-1.
Academic Article Preventing stroke in sickle cell anemia.
Academic Article Cation depletion by the sodium pump in red cells with pathologic cation leaks. Sickle cells and xerocytes.
Academic Article Hydroxyurea enhances fetal hemoglobin production in sickle cell anemia.
Academic Article Exercise-induced hemolysis in sickle cell anemia: shear sensitivity and erythrocyte dehydration.
Academic Article The acute chest syndrome of sickle cell disease.
Academic Article Protective effects of phosphodiesterase-4 (PDE-4) inhibition in the early phase of pulmonary arterial hypertension in transgenic sickle cell mice.
Academic Article Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy.
Academic Article Is there treatment for sickle cell anemia?
Academic Article Mammalian reticulocytes lose adhesion to fibronectin during maturation to erythrocytes.
Academic Article Bone marrow transplantation in sickle cell anemia--the dilemma of choice.
Academic Article Silent cerebral infarcts in sickle cell anemia: a risk factor analysis. The Cooperative Study of Sickle Cell Disease.
Academic Article Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia.
Academic Article Membrane protein interactions in sickle red blood cells: evidence of abnormal protein 3 function.
Academic Article Lung function in children with sickle cell anemia.
Academic Article Energy reserve and cation composition of irreversibly sickled cells in vivo.
Academic Article HPLC measurement, blood distribution, and pharmacokinetics of oral clotrimazole, potentially useful antisickling agent.
Academic Article Mortality in sickle cell disease. Life expectancy and risk factors for early death.
Academic Article Therapy with oral clotrimazole induces inhibition of the Gardos channel and reduction of erythrocyte dehydration in patients with sickle cell disease.
Academic Article Hydroxyurea increases fetal hemoglobin production in sickle cell anemia.
Academic Article Prevention and management of stroke in sickle cell anemia.
Academic Article Influence of hydroxyurea on fetal hemoglobin production in vitro.
Academic Article Pulmonary hypertension and nitric oxide depletion in sickle cell disease.
Academic Article Sickle cell paths converge on hydroxyurea.
Academic Article Chemotherapy to increase fetal hemoglobin in patients with sickle cell anemia.
Academic Article Sickle cell anemia as an inflammatory disease.
Academic Article A new therapeutic approach for sickle cell disease. Blockade of the red cell Ca(2+)-activated K+ channel by clotrimazole.
Academic Article Pain in sickle cell disease. Rates and risk factors.
Academic Article Easing the suffering caused by sickle cell disease.
Concept Hemoglobin SC Disease
Concept Anemia, Sickle Cell
Grant USE OF HYDROXYUREA IN SICKLE CELL ANEMIA
Grant COMPREHENSIVE SICKLE CELL CENTER
Grant GENETIC MODIFIERS OF SEVERITY IN SICKLE CELL ANEMIA
Academic Article Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort.
Search Criteria
  • Anemia Sickle Cell
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.