parvovirus b19 infections in paediatric sickle cell disease patients genotype and hydroxyurea treatment influence disease severity

Original title: “Parvovirus B19 infections in paediatric sickle cell disease patients: Genotype and hydroxyurea treatment influence disease severity.”

metabolic dysregulation linked to sickling tendency in sickle cell anemia independent of hbf

Original title: “Metabolic dysregulation linked to sickling tendency in sickle cell anemia independent of HbF.”

clinical base editing for hemoglobinopathies across different genetic backgrounds

Original title: “Clinical base editing for β-hemoglobinopathies across different genetic backgrounds.”

rare and underrecognized complication of sickle cell disease in a pediatric patient acute soft head syndrome

Original title: “A rare and underrecognized complication of sickle cell disease in a pediatric patient: acute soft head syndrome.”

lesser known medication safety considerations in sickle cell disease

Original title: “Lesser-known medication safety considerations in sickle cell disease.”

characteristics of donor and recipient clonal hematopoiesis in nonmyeloablative transplant for sickle cell disease

Original title: “Characteristics of Donor and Recipient Clonal Hematopoiesis in Nonmyeloablative Transplant for Sickle Cell Disease.”

orbital compression syndrome mimicking severe malaria in a child with sickle cell disease in a ugandan refugee settlement a case report

Original title: “Orbital Compression Syndrome Mimicking Severe Malaria in a Child with Sickle Cell Disease in a Ugandan Refugee Settlement: A Case Report.”

hydromorphone induced choreiform dyskinesia in a patient with homozygous sickle cell disease a reversible adverse effect

Original title: “Hydromorphone-induced choreiform dyskinesia in a patient with homozygous sickle cell disease: a reversible adverse effect.”

humanistic and economic burden among caregivers of adults and children with sickle cell disease and recurrent vaso occlusive crises

Original title: “Humanistic and economic burden among caregivers of adults and children with sickle cell disease and recurrent vaso-occlusive crises.”