British Journal of Haematology

Striking bone marrow plasmacytosis in a patient with sickle cell anaemia
pp. 457-457(1)
Authors: Bayley, Jake; Pavlů, Jiří; Thompson, Mary

Paraneoplastic pemphigus associated with follicular lymphoma
pp. 458-458(1)
Authors: Lachenal, Florence; Amini, Mona; Salino, Samuel; Biron, Pierre

Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (CSF3R) mutations in severe congenital neutropenia
pp. 459-467(9)
Authors: Zeidler, Cornelia; Germeshausen, Manuela; Klein, Christoph; Welte, Karl

Optimal management of adults with ALL
pp. 468-483(16)
Author: Rowe, Jacob M.

A comparative study of bone marrow and peripheral blood CD34⁺ myeloblasts in acute myeloid leukaemia
pp. 484-491(8)
Authors: Cheung, Alice M. S.; Chow, Howard C. H.; Liang, Raymond; Leung, Anskar Y. H.

Molecular and clinical features of chronic lymphocytic leukaemia with stereotyped B cell receptors: results from an Italian multicentre study
pp. 492-506(15)
Authors: Bomben, Riccardo; Dal Bo, Michele; Capello, Daniela; Forconi, Francesco; Maffei, Rossana; Laurenti, Luca; Rossi, Davide; Del Principe, Maria Ilaria; Zucchetto, Antonella; Bertoni, Francesco; Rossi, Francesca Maria; Bulian, Pietro; Cattarossi, Ilaria; Ilariucci, Fiorella; Sozzi, Elisa; Spina, Valeria; Zucca, Emanuele; Degan, Massimo; Lauria, Francesco; Del Poeta, Giovanni; Efremov, Dimitar G.; Marasca, Roberto; Gaidano, Gianluca; Gattei, Valter

Expression and function of toll like receptors in chronic lymphocytic leukaemia cells
pp. 507-516(10)
Authors: Muzio, Marta; Scielzo, Cristina; Bertilaccio, Maria T. S.; Frenquelli, Michela; Ghia, Paolo; Caligaris-Cappio, Federico

Monitoring minimal residual disease in acute myeloid leukaemia with NPM1 mutations by quantitative PCR: clonal evolution is a limiting factor
pp. 517-523(7)
Authors: Papadaki, Christina; Dufour, Annika; Seibl, Marlene; Schneider, Stephanie; Bohlander, Stefan K.; Zellmeier, Evelyn; Mellert, Gudrun; Hiddemann, Wolfgang; Spiekermann, Karsten

High-dose Ara-C and beam with autograft rescue in R-CHOP responsive mantle cell lymphoma patients
pp. 524-530(7)
Authors: van 't Veer, Mars B.; de Jong, Daphne; MacKenzie, Marius; Kluin-Nelemans, Hanneke C.; van Oers, Marinus H. J.; Zijlstra, Jose; Hagenbeek, Anton; van Putten, Wim L. J.

The Stanford V regimen is effective in patients with good risk Hodgkin lymphoma but radiotherapy is a necessary component
pp. 531-537(7)
Authors: Abuzetun, Jamil Y.; Loberiza, Fausto; Vose, Julie; Bierman, Philip; Greg Bociek, R.; Enke, Charles; Bast, Martin; Weisenburger, Dennis; Armitage, James O.

The role of X-inactivation in the gender bias of patients with acquired α-thalassaemia and myelodysplastic syndrome (ATMDS)
pp. 538-545(8)
Authors: Haas, Peter S.; Roy, Noemi B. A.; Gibbons, Richard J.; Deville, Marie-Alice; Fisher, Chris; Schwabe, Michael; Bissé, Emmanuel; van Dorsselaer, Alain; Higgs, Douglas R.; Lübbert, Michael

The t(X;7)(q22;q34) in paediatric T-cell acute lymphoblastic leukaemia results in overexpression of the insulin receptor substrate 4 gene through illegitimate recombination with the T-cell receptor beta locus
pp. 546-551(6)
Authors: Karrman, Kristina; Kjeldsen, Eigil; Lassen, Carin; Isaksson, Margareth; Davidsson, Josef; Andersson, Anna; Hasle, Henrik; Fioretos, Thoas; Johansson, Bertil

Long-term follow-up analysis after rituximab therapy in children with refractory symptomatic ITP: identification of factors predictive of a sustained response
pp. 552-558(7)
Authors: Parodi, Emilia; Rivetti, Elisa; Amendola, Giovanni; Bisogno, Gianni; Calabrese, Roberto; Farruggia, Piero; Giordano, Paola; Rosaria Matarese, Sofia Maria; Nardi, Margherita; Nobili, Bruno; Notarangelo, Lucia D.; Russo, Giovanna; Vimercati, Chiara; Zecca, Marco; De Mattia, Domenico; Ramenghi, Ugo

Long-term outcome of initially homogenously treated and relapsed childhood acute lymphoblastic leukaemia in Austria - A population-based report of the Austrian Berlin-Frankfurt-Münster (BFM) Study Group
pp. 559-570(12)
Authors: Reismüller, Bettina; Attarbaschi, Andishe; Peters, Christina; Dworzak, Michael N.; Pötschger, Ulrike; Urban, Christian; Fink, Franz-Martin; Meister, Bernhard; Schmitt, Klaus; Dieckmann, Karin; Henze, Günter; Haas, Oskar A.; Gadner, Helmut; Mann, Georg

Manufacturing of human placenta-derived mesenchymal stem cells for clinical trials
pp. 571-579(9)
Authors: Brooke, Gary; Rossetti, Tony; Pelekanos, Rebecca; Ilic, Nina; Murray, Patricia; Hancock, Sonia; Antonenas, Vicki; Huang, Gillian; Gottlieb, David; Bradstock, Ken; Atkinson, Kerry

Compartmentalization regulates the interaction between the platelet integrin α_IIbβ₃ and ICln
pp. 580-590(11)
Authors: Larkin, Deirdre; Treumann, Achim; Murphy, Derek; DeChaumont, Ciaran; Kiernan, Aoife; Moran, Niamh

Phosphatidylserine surface expression and integrin αIIbβ3 activity on thrombin/convulxin stimulated platelets/particles of different sizes
pp. 591-602(12)
Authors: Rukoyatkina, Natalia; Begonja, Antonija J.; Geiger, Jörg; Eigenthaler, Martin; Walter, Ulrich; Gambaryan, Stepan

Expansion of haematopoietic stem cells from normal donors and bone marrow failure patients by recombinant hoxb4
pp. 603-612(10)
Authors: Tang, Yong; Chen, Jichun; Young, Neal S.

The role of Epstein-Barr virus in Richter syndrome
pp. 613-613(1)
Authors: Nourse, Jamie; Jones, Kimberley; Gandhi, Maher K.

The role of Epstein-Barr virus in Richter syndrome: response to Nourse et al
pp. 614-615(2)
Authors: Omoti, Caroline Edijana; Omoti, Afekhide Ernest

Complex inheritance of chronic haemolytic anaemia
pp. 615-616(2)
Authors: Coutinho, Rita; Bento, Celeste; Almeida, Helena; Cunha, Elisabete; Manco, Licínio; Ferreira, Fátima; Ribeiro, M. Letícia

Improving management of neutropenic sepsis in the emergency department
pp. 617-618(2)
Authors: Richardson, Simon; Pallot, David; Hughes, Tom; Littlewood, Timothy

Immature platelet fraction as novel laboratory parameter predicting the course of neonatal thrombocytopenia
pp. 619-621(3)
Authors: Cremer, Malte; Paetzold, Judith; Schmalisch, Gerd; Hammer, Hannes; Loui, Andrea; Dame, Christof; Weimann, Andreas

Anti-Fy3 in sickle cell disease: a difficult transfusion problem
pp. 621-622(2)
Authors: Went, Richard; Wright, Josh; Webster, Robert; Stamps, Robert

Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF
pp. 622-624(3)
Authors: Ament, Andrea E.; Li, Zhongyuan; Sturm, Amy C.; Perko, James D.; Lawson, Sarah; Masterson, Margaret; Quadros, Edward V.; Tanner, Stephan M.

Corrigendum
pp. 625-625(1)

Transfusion Microbiology
pp. 626-626(1)
Author: Murphy, Mike