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Acute chest syndrome in sickle cell disease: clinical presentation and course. Cooperative Study of Sickle Cell Disease.
Clincal, 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.