British Journal of Haematology

Papers to be published in forthcoming issues
pp. x-x(1)

Congenital mitral stenosis presenting with haemolytic anaemia
pp. 579-579(1)

¹⁸F-fluorodeoxyglucose positron emission tomography/computed tomography in the evaluation of early response in a primary hepatic lymphoma
pp. 580-580(1)

A review of the scientific and literary accomplishments of Professor R.G. Macfarlane CBE, FRS
pp. 581-590(10)
Author: Hougie, Cecil

The diagnosis and management of factor VIII and IX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors Organisation
pp. 591-605(15)
Authors: Hay, Charles R. M.; Brown, S.; Collins, P. W.; Keeling, D. M.; Liesner, R.

Treatment of severe aplastic anaemia with combined immunosuppression: anti-thymocyte globulin, ciclosporin and mycophenolate mofetil
pp. 606-611(6)
Authors: Scheinberg, Phillip; Nunez, Olga; Wu, Colin; Young, Neal S.

Transformed diffuse large B-cell lymphomas with gains of the discontinuous 12q12-14 amplicon display concurrent deregulation of CDK2, CDK4 and GADD153 genes
pp. 612-621(10)
Authors: Al-Assar, Osama; Rees-Unwin, Karen S.; Menasce, Lia P.; Hough, Rachael E.; Goepel, John R.; Hammond, David W.; Hancock, Barry W.

Retreatment with rabbit anti-thymocyte globulin and ciclosporin for patients with relapsed or refractory severe aplastic anaemia
pp. 622-627(6)
Authors: Scheinberg, Phillip; Nunez, Olga; Young, Neal S.

Timing of autologous stem cell transplantation from last chemotherapy affects lymphocyte collection and survival in non-Hodgkin lymphoma
pp. 628-633(6)
Authors: Holtan, Shernan G.; Porrata, Luis F.; Inwards, David J.; Ansell, Stephen M.; Micallef, Ivana N.; Johnston, Patrick B.; Litzow, Mark R.; Gastineau, Dennis A.; Markovic, Svetomir N.

Haematopoietic stem cell transplantation as primary therapy of sporadic adult Burkitt lymphoma
pp. 634-637(4)
Authors: Song, Kevin W.; Barnett, Michael J.; Gascoyne, Randy D.; Horsman, Douglas E.; Forrest, Donna L.; Hogge, Donna E.; Lavoie, Julyle C.; Nantel, Stephen H.; Nevill, Thomas J.; Shepherd, John D.; Smith, Clayton A.; Sutherland, Heather J.; Voss, Nicholas J.; Toze, Cynthia L.; Connors, Joseph M.

C-terminal nucleophosmin mutations are uncommon in chronic myeloid disorders
pp. 638-641(4)
Authors: Caudill, Jonathan S. C.; Sternberg, Alexander J.; Li, Chin-Yang; Tefferi, Ayalew; Lasho, Terra L.; Steensma, David P.

Overexpression of the VAV proto-oncogene product is associated with B-cell chronic lymphocytic leukaemia displaying loss on 13q
pp. 642-645(4)
Authors: Prieto-Sánchez, Rosario M.; Hernández, José A.; García, Juan L.; Gutiérrez, Norma C.; Miguel, Jesús San; Bustelo, Xosé R.; Hernández, Jesús M.

Long-term results of an ultra low-dose cytarabine-based regimen for the treatment of acute megakaryoblastic leukaemia in children with Down syndrome
pp. 646-648(3)
Authors: Al-Ahmari, Ali; Shah, Niketa; Sung, Lillian; Zipursky, Alvin; Hitzler, Johann

Allogeneic stem cell transplantation for severe acquired aplastic anaemia using a fludarabine-based preparative regimen
pp. 649-654(6)
Authors: Resnick, Igor B.; Aker, Memet; Shapira, Michael Y.; Tsirigotis, Panagiotis D.; Bitan, Menachem; Abdul-Hai, Ali; Samuel, Simcha; Ackerstein, Aliza; Gesundheit, Benjamin; Zilberman, Irina; Miron, Svetlana; Yoffe, Luba; Lvovich, Alex; Slavin, Shimon; Or, Reuven

Measurement of von Willebrand factor binding to a recombinant fragment of glycoprotein Ibα in an enzyme-linked immunosorbent assay-based method: performances in patients with type 2B von Willebrand disease
pp. 655-663(9)
Authors: Caron, Claudine; Hilbert, Lysiane; Vanhoorelbeke, Karen; Deckmyn, Hans; Goudemand, Jenny; Mazurier, Claudine

Distinguishing between type 2B and pseudo-von Willebrand disease and its clinical importance
pp. 664-666(3)
Authors: Enayat, Mohammad S.; Guilliatt, Andrea M.; Lester, William; Wilde, Jonathan T.; Williams, Michael D.; Hill, Frank G.H.

Severe infections in thalassaemic patients: prevalence and predisposing factors
pp. 667-674(8)
Authors: Rahav, Galia; Volach, Vania; Shapiro, Mervyn; Rund, Deborah; Rachmilewitz, Eliezer A.; Goldfarb, Ada

α-Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β-thalassaemia
pp. 675-682(8)
Authors: Lai, Mei I.; Jiang, Jie; Silver, Nicholas; Best, Steve; Menzel, Stephan; Mijovic, Aleksandar; Colella, Stefano; Ragoussis, Jiannis; Garner, Chad; Weiss, Mitchell J.; Thein, Swee L.

Pyruvate kinase deficiency in France: a 3-year study reveals 27 new mutations
pp. 683-689(7)
Authors: Pissard, Serge; Max-Audit, Isabelle; Skopinski, Laurent; Vasson, Aurélie; Vivien, Pascal; Bimet, Catherine; Goossens, Michel; Galacteros, Frederic; Wajcman, Henri

101 years of McCrae's (not Auer's) rods
pp. 690-690(1)

Plasma as a source of mRNA for determining IgV_H mutation status in patients with chronic lymphocytic leukaemia
pp. 690-692(3)

Increased CA-15.3 levels in the serum of patients with homozygous β-thalassaemia and sickle cell/β-thalassaemia
pp. 692-694(3)

Author index
pp. 695-697(3)

Keyword index
pp. 698-700(3)