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X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.
Pulmonary hypertension and NO in sickle cell.
Management of chronic viral hepatitis in patients with thalassemia: recommendations from an international panel.
The effect of deferasirox on cardiac iron in thalassemia major: impact of total body iron stores.
Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome.
Use of chromosome engineering to model a segmental deletion of chromosome band 7q22 found in myeloid malignancies.
Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury.
Mutations in CBL occur frequently in juvenile myelomonocytic leukemia.
The graft-versus-leukemia effect using matched unrelated donors is not superior to HLA-identical siblings for hematopoietic stem cell transplantation.
A retroviral mutagenesis screen reveals strong cooperation between Bcl11a overexpression and loss of the Nf1 tumor suppressor gene.