Guidelines for pediatric management of severe chronic neutropenia
Intravenous or oral iron?
Pruritus in primary myelofibrosis : Clinical and laboratory correlates
Electrocardiographic consequences of cardiac iron overload in thalassemia major
Thrombin generation reveals high procoagulant potential in the plasma of sickle cell disease children
Response-adjusted ISS (RaISS) is a simple and reliable prognostic scoring system for predicting progression-free survival in transplanted patients with multiple myeloma
Pancreatic iron and glucose dysregulation in thalassemia major
Polymorphism in the protease-activated receptor-4 gene region associates with platelet activation and perioperative myocardial injury
Pituitary iron and volume predict hypogonadism in transfusional iron overload
Retrospective analysis of weekly intravenous immunoglobulin prophylaxis versus intravenous immunoglobulin by IgG level monitoring in hematopoietic stem cell transplant recipients
Environmental, lifestyle, and familial/ethnic factors associated with myeloproliferative neoplasms
Immunoglobulin light chain amyloidosis : 2012 update on diagnosis, prognosis, and treatment
Malaria – one swallow makes a summer
Systemic mastocytosis with associated clonal hematological non-mast-cell lineage disease : A case review
Test of the month : The chromogenic antifactor Xa assay
Leukocytosis : The mysteries within
Uveitis as the initial manifestation of diffuse large B-cell lymphoma
Peripheral blood and bone marrow findings in B-cell lymphoma, unclassifiable with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma
Blood tests may predict early primary myelofibrosis in patients presenting with essential thrombocythemia
TP53 mutations and polymorphisms in primary myelofibrosis
Relative efficacy of steroid therapy in immune thrombocytopenia mediated by anti-platelet GPIIbIIIa versus GPIbα antibodies
Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous : Description of seven new G6PD mutants
Treatment of molecular relapse in patients with acute myeloid leukemia using clofarabine monotherapy
The potential role of pre-transplant HBcIgG seroposivity as predictor of clinically relevant cytomegalovirus infection in patients with lymphoma undergoing autologous hematopoietic stem cell transplantation : A study from the Rome Transplant Network
Fetal hemoglobin in sickle cell anemia : Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans
Spontaneous graft versus host disease occurring in a patient with multiple myeloma after autologous stem cell transplant
Transfusional iron overload in children with sickle cell anemia on chronic transfusion therapy for secondary stroke prevention
Complications of implantable venous access devices in patients with sickle cell disease
Inhibition of cell-mediated immunity by the histone deacetylase inhibitor vorinostat : Implications for therapy of cutaneous T-cell lymphoma
The diagnostic value of biopsy of small peripheral lymph nodes in patients with suspected lymphoma
Safety of plasma-derived protein C for treating disseminated intravascular coagulation in adult patients with active cancer
Severe hypocalcemia and drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome under deferasirox therapy for myelodysplasic syndrome
Comment on : Neutropenia and anemia with reduced serum vitamin B(12)
Clinical trial opportunities in hemostasis and thrombosis : NHBLI State-of-the-science symposium
Congenital and acquired neutropenias consensus guidelines on therapy and follow-up in childhood from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica)