Long-term experience with imatinib therapy in chronic phase chronic myelogenous leukemia—Remarkable activity with room for improvement
Sustained remissions and low rate of BCR-ABL resistance mutations with imatinib treatment chronic myelogenous leukemia in patients treated in late chronic phase: A 5-year follow up
Combination chemotherapy with low-dose cytarabine, homoharringtonine, and granulocyte colony-stimulating factor priming in patients with relapsed or refractory acute myeloid leukemia
Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations
Evaluation of opioid induced nausea and vomiting in sickle cell disease
UGT2B7 promoter variant -840G>A contributes to the variability in hepatic clearance of morphine in patients with sickle cell disease
The prognostic significance of leukemic cells clearance kinetics evaluation during the initial course of induction therapy with HAD (homoharringtonine, cytosine arabinoside, daunorubicin) in patients with de novo acute myeloid leukemia
Transendothelial migration of leukocytes is promoted by plasma from a subgroup of immune thrombocytopenic purpura patients with small-vessel ischemic brain disease
Utility of consecutive repeat HIT ELISA testing for heparin-induced thrombocytopenia
Nodular lymphocyte predominant Hodgkin lymphoma at atypical locations may be associated with increased numbers of large cells and a diffuse histologic component
Soluble TWEAK is markedly elevated in hemophagocytic lymphohistiocytosis
Decreased incidence of acute graft-versus-host disease by continuous infusion of cyclosporine with a higher target blood level
Pharmacogenetics of morphine: Potential implications in sickle cell disease
Testing for recombinant erythropoietin
Hypersplenism induced by splenic vein ligation
Prolonged half-life of Argatroban in patients with renal dysfunction and antiphospholipid antibody syndrome being treated for heparin-induced thrombocytopenia
Late onset of autoimmune hemolytic anemia and pure red cell aplasia after allogeneic hematopoietic stem cell transplantation using in vivo alemtuzumab
Superficial venous thrombosis associated with congenital absence of the inferior vena cava and previous episode of deep venous thrombosis
Hypertriglyceridemia presenting as “pink blood” and elevated hemoglobin level
Weisses Blut— Leukapheresis in acute leukemia
Diagnosis of thrombotic thrombocytopenic purpura with normal ADAMTS13 activity and absence of its inhibitor (anti-ADAMTS13 antibodies)
Response to Boctor and Smith
Hemoglobin—E β thalassemia presenting with recurrent priapism—a rare complication
The erythrocyte mean corpuscular volume is associated with serum levels of thyroid stimulating hormone in women