Neuropathy, neuropathic pain, and sickle cell disease
Stimulating erythropoiesis in neonates
Pain and other non-neurological adverse events in children with sickle cell anemia and previous stroke who received hydroxyurea and phlebotomy or chronic transfusions and chelation: Results from the SWiTCH clinical trial
Pain over time and its effects on life in thalassemia
Safety and efficacy of total dose infusion of 1,020 mg of ferumoxytol administered over 15 min
Genome wide SNP array identified multiple mechanisms of genetic changes in Waldenstrom macroglobulinemia
Bendamustine in chronic lymphocytic leukemia: Outcome according to different clinical and biological prognostic factors in the everyday clinical practice
Clofarabine, idarubicin, and cytarabine (CIA) as frontline therapy for patients ≤60 years with newly diagnosed acute myeloid leukemia
Chronic myelomonocytic leukemia: 2013 update on diagnosis, risk stratification, and management
The peripheral blood features of acute myeloid leukemia with inv(16)(p13.1q22)
Peering into the future: Hepcidin testing
Skin involvement with Hodgkin disease: A rare condition late in the course of Hodgkin lymphoma
Variation in chitotriosidase values measured on simultaneous samples by two commercial laboratories
Multiplicative interaction between mean corpuscular volume and red cell distribution width in predicting mortality of elderly patients with and without anemia
Liver stiffness increases acutely during sickle cell vaso-occlusive crisis
A dose-escalation phase IIa study of 2,2-dimethylbutyrate (HQK-1001), an oral fetal globin inducer, in sickle cell disease
Cerebrovascular events in sickle cell-beta thalassemia treated with hydroxyurea: A single center prospective survey in adult Italians
Evaluation of the role of secretory sphingomyelinase and bioactive sphingolipids as biomarkers in hemophagocytic lymphohistiocytosis
Fludarabine-mitoxantrone-rituximab regimen in untreated intermediate/high-risk follicular non-Hodgkin's lymphoma: Experience on 142 patients
Clinical implications of U2AF1 mutation in patients with myelodysplastic syndrome and its stability during disease progression
Tissue iron evaluation in chronically transfused children shows significant levels of iron loading at a very young age