Thalassemiabeta-ThalassemiaHemoglobin Ealpha-ThalassemiaFetal HemoglobinGlobinsHemoglobinopathiesHemoglobin A2alpha-GlobinsChelation TherapyHemoglobin JSicilyArabiaHemoglobins, AbnormalHemoglobin AIron OverloadHemoglobinometryErythrocytes, AbnormalBlood TransfusionAnemia, Sickle CellPostoperative ComplicationsHemoglobinsHomozygoteErythrocyte CountErythrocyte IndicesHeterozygote DetectionReticulocytesSplenectomyErythropoiesisIron Chelating AgentsFerritinsHeterozygoteErythrocytesErythrocyte MembraneDeferoxaminePyridones5'-NucleotidaseInterleukin-1betabeta-GlobinsBase SequenceMutationHemoglobin HTreatment OutcomeBone Marrow Transplantationbeta 2-MicroglobulinIndiaPhenotypeIronRetrospective StudiesIntraoperative ComplicationsSickle Cell TraitReceptors, Adrenergic, betaIntegrin beta3HemosiderosisTime Factorsdelta-ThalassemiaFollow-Up StudiesHemoglobin, SickleProspective StudiesDiabetes ComplicationsRisk FactorsTransforming Growth Factor betaOsmotic FragilityAnemia, HypochromicItalyHemoglobin CPregnancy ComplicationsRNA, MessengerHematopoiesis, ExtramedullaryPregnancyAnemiaIntegrin alpha5beta1Integrin beta4beta 2-Glycoprotein IBenzoatesLiverReoperationIntegrin alpha6beta4delta-GlobinsIntegrin beta ChainsErythrocyte AgingEndocrine System DiseasesHemoglobin SC DiseaseElectronics, MedicalHemoglobin C DiseaseInfant, NewbornIntegrin alpha4beta1GenotypeGenesErythrocyte TransfusionCells, CulturedMelanesiaIntegrin alpha2beta1Receptors, Adrenergic, beta-2