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Haematologica|May 30, 2013
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal rangeSilverio Perrotta, Daniel P Stiehl, Francesca Punzo, et al.
Haematologica|May 2, 2013
Clinical implications of the molecular genetics of chronic lymphocytic leukemiaRobin Foà, Ilaria Del Giudice, Anna Guarini, et al.
Haematologica|June 12, 2013
Inhibiting Polo-like kinase 1 causes growth reduction and apoptosis in pediatric acute lymphoblastic leukemia cellsStefanie A Hartsink-Segers, Carla Exalto, Matthew Allen, et al.
Haematologica|November 12, 2013
Allogeneic stem cell transplantation for advanced cutaneous T-cell lymphomas: a study from the French Society of Bone Marrow Transplantation and French Study Group on Cutaneous LymphomasAdèle de Masson, Marie Beylot-Barry, Jean-David Bouaziz, et al.
Haematologica|November 12, 2013
Oral melphalan and dexamethasone grants extended survival with minimal toxicity in AL amyloidosis: long-term results of a risk-adapted approachGiovanni Palladini, Paolo Milani, Andrea Foli, et al.
Haematologica|October 29, 2013
Autologous stem cell transplantation after conditioning with yttrium-90 ibritumomab tiuxetan plus BEAM in refractory non-Hodgkin diffuse large B-cell lymphoma: results of a prospective, multicenter, phase II clinical trialJavier Briones, Silvana Novelli, José A García-Marco, et al.
Haematologica|October 29, 2013
Comparison of horse and rabbit antithymocyte globulin in immunosuppressive therapy for refractory cytopenia of childhoodAyami Yoshimi, Marry M van den Heuvel-Eibrink, Irith Baumann, et al.
Haematologica|August 6, 2013
High CD45 surface expression determines relapse risk in children with precursor B-cell and T-cell acute lymphoblastic leukemia treated according to the ALL-BFM 2000 protocolGunnar Cario, Peter Rhein, Rita Mitlöhner, et al.
Haematologica|October 1, 2013
Novel exon 2 α spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct α spectrin defectsSabina Swierczek, Archana M Agarwal, Kubendran Naidoo, et al.
Haematologica|October 1, 2013
Acquired ASXL1 mutations are common in patients with inherited GATA2 mutations and correlate with myeloid transformationRobert R West, Amy P Hsu, Steven M Holland, et al.
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