Thalassemiabeta-Thalassemiaalpha-ThalassemiaHemoglobin EChelation TherapySeverity of Illness IndexGlobinsIron OverloadHemoglobins, AbnormalHemoglobinopathiesIron Chelating AgentsHemoglobin A2alpha-GlobinsFetal HemoglobinBlood TransfusionDeferoxaminePyridonesbeta-GlobinsAnemia, Sickle CellHemoglobin HSicilyIronHemoglobin JHomozygoteErythrocyte CountErythrocytes, AbnormalFerritinsSickle Cell TraitHeterozygoteHemoglobinsErythrocyte IndicesHemosiderosisHemoglobin AReticulocytesdelta-ThalassemiaHemoglobinometryErythropoiesisSplenectomyHemoglobin, SickleErythrocytesHeterozygote DetectionAnemia, HypochromicOsmotic FragilityItalyHemoglobin CHematopoiesis, ExtramedullaryInjury Severity ScoreGenotypeArabiadelta-GlobinsPhenotypeErythrocyte AgingBenzoatesAnemiaElectronics, MedicalHemoglobin C DiseaseHemoglobin SC DiseaseThailandMutationMelanesiaHemochromatosisEndocrine System DiseasesTreatment OutcomeHemosiderinSiderophoresProspective StudiesPedigreeErythrocyte TransfusionLiverTrauma Severity IndicesRetrospective StudiesPrenatal DiagnosisChromosome DeletionBlood Protein ElectrophoresisHeinz BodiesPrevalenceHemolysisgamma-GlobinsGenesErythrocyte DeformabilityCyprusErythroid Precursor CellsBase SequenceAnemia, HemolyticMagnetic Resonance ImagingBone Marrow TransplantationIron, DietaryAge FactorsTime FactorsRisk FactorsGilbert Disease