Myeloma crystal tubulopathy and Fanconi syndrome: a rare histological finding
Strongyloides stercoralis hyperinfection in a patient treated for multiple myeloma
Diagnosis and management of maternal thrombocytopenia in pregnancy
Short- and long-term risks of splenectomy for benign haematological disorders: should we revisit the indications?
Diagnosis and management of acute graft-versus-host disease
Diagnosis and management of chronic graft-versus-host disease
Organ-specific management and supportive care in chronic graft-versus-host disease
A rare fraction of drug-resistant follicular lymphoma cancer stem cells interacts with follicular dendritic cells to maintain tumourigenic potential
Outcome disparities in multiple myeloma: a SEER-based comparative analysis of ethnic subgroups
Long-term follow-up of myelodysplastic syndrome patients with moderate/severe anaemia receiving human recombinant erythropoietin + 13- cis -retinoic acid and dihydroxylated vitamin D3: independent positive impact of erythroid response on survival
Phase II study of sorafenib in patients with relapsed or refractory lymphoma
Success of allogeneic marrow transplantation for children with severe aplastic anaemia
De novo childhood myelodysplastic/myeloproliferative disease with unique molecular characteristics
Large deletion in the Factor VIII gene ( F8 ) involving segmental duplications in int22h shows no haematological phenotype in female carriers, but may be embryonic lethal in males
Decreased bone density and bone strength in a mouse model of severe factor VIII deficiency
A Chinese family carrying novel mutations in SEC23B and HFE2 , the genes responsible for congenital dyserythropoietic anaemia II (CDA II) and primary iron overload, respectively
Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia
Safety and efficacy of a long-acting liposomal formulation of plasma-derived factor VIII in haemophilia A patients