Hermansky-Pudlak syndrome
Haemophagocytic syndrome associated with Hodgkin lymphoma and Pneumocystis jiroveci pneumonitis
Consensus recommendations
Recommendations for the management of the haematological and onco-haematological aspects of Gaucher disease1
FLT3 inhibition in acute myeloid leukaemia
Waldenström macroglobulinaemia
CD154 induces a switch in pro-survival Bcl-2 family members in chronic lymphocytic leukaemia
Frequent occurrence of B-cell lymphomas in angioimmunoblastic T-cell lymphoma and proliferation of Epstein–Barr virus-infected cells in early cases
High expression of connective tissue growth factor in pre-B acute lymphoblastic leukaemia
Somatically mutated immunoglobulin IGHV@ genes without intraclonal heterogeneity indicate a postgerminal centre origin of primary intraocular diffuse large B-cell lymphomas
Dysregulation of CD47 and the ligands thrombospondin 1 and 2 in multiple myeloma
Outcome of children with nodular lymphocyte predominant Hodgkin lymphoma – a Children's Cancer and Leukaemia Group report
Elevated endogenous thrombin potential is associated with an increased risk of a first deep venous thrombosis but not with the risk of recurrence
Measurement of global haemostasis in severe haemophilia A following factor VIII infusion
Inhibition of Akt induces significant downregulation of survivin and cytotoxicity in human multiple myeloma cells
Haematopoietic stem cells participate in muscle regeneration
Establishment and exploitation of hyperdiploid and non-hyperdiploid human myeloma cell lines
Striking response to intrathecal liposomal cytarabine in a patient with meningeal myelomatosis
JAK2V617F in idiopathic venous thromboembolism occurring in the absence of inherited or acquired thrombophilia
Splenic peliosis and rupture in patients with dyskeratosis congenita on androgens and granulocyte colony-stimulating factor
Trisomy 11 with MLL-PTD in a case of infant AML M0
Haemangioblastic transformation of myeloproliferative disease?
Amendment to the guideline for diagnosis and investigation of polycythaemia/erythrocytosis
The disappearance of two alleles of JAK2 V617F from peripheral blood of a polycythaemia vera patient correlates with transformation into myelofibrosis
Platelets, 2nd Edition