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Stroke and conversion to high risk in children screened with transcranial Doppler ultrasound during the STOP study.
Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis.
Gene interactions and stroke risk in children with sickle cell anemia.
Deferiprone and hepatic fibrosis.
Prenatal origin of childhood acute myeloid leukemias harboring chromosomal rearrangements t(15;17) and inv(16).
Platelet factor 4 enhances generation of activated protein C in vitro and in vivo.
Distinct HLA associations by stroke subtype in children with sickle cell anemia.
Hematologic effects of inactivating the Ras processing enzyme Rce1.
Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease.
Comprehensive banking of sibling donor cord blood for children with malignant and nonmalignant disease.