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Clinical, immunologic, and genetic features of an autoimmune lymphoproliferative syndrome associated with abnormal lymphocyte apoptosis.
First report of reversal of organ dysfunction in sickle cell anemia by the use of hydroxyurea: splenic regeneration.
A point mutation in the catalytic domain of c-kit induces growth factor independence, tumorigenicity, and differentiation of mast cells.
Retroviral-mediated gene correction for X-linked severe combined immunodeficiency.
Phospholipase A2 levels in acute chest syndrome of sickle cell disease.
Induction of tolerance in nondefective mice after in utero transplantation of major histocompatibility complex-mismatched fetal hematopoietic stem cells.
Surgery and anesthesia in sickle cell disease. Cooperative Study of Sickle Cell Diseases.
Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease.
Neurologic complications after allogeneic marrow transplantation for sickle cell anemia.
Pulmonary fat embolism: a distinct cause of severe acute chest syndrome in sickle cell anemia.