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Haematologica|August 4, 2006
Out of hospital treatment with subcutaneous low molecular weight heparin in patients with acute deep-vein thrombosis: a prospective study in daily practiceMajida Zidane, Leonard H van Hulsteijn, Bernard J Brenninkmeijer, et al.
Haematologica|August 23, 2006
Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overloadS Majore, F Milano, F Binni, et al.
Haematologica|August 4, 2006
The role of HLA mismatch, splenectomy and recipient Epstein-Barr virus seronegativity as risk factors in post-transplant lymphoproliferative disorder following allogeneic hematopoietic stem cell transplantationMikael Sundin, Katarina Le Blanc, Olle Ringdén, et al.
Haematologica|August 4, 2006
Combination erythropoietin-hydroxyurea therapy in sickle cell disease: experience from the National Institutes of Health and a literature reviewJane A Little, Vicki R McGowan, Gregory J Kato, et al.
Haematologica|August 4, 2006
Osteonecrosis after allogeneic stem cell transplantation in childhood. A case-control study in ItalyMaura Faraci, Maria Grazia Calevo, Edoardo Lanino, et al.
Haematologica|August 23, 2006
Transient loss of the Y-chromosome in an elderly man with anemia and lead poisoning: chance occurrence or a clonal marker of the underlying hematological abnormality?Elpis Mantadakis, Anna M Boula, George Girakis, et al.
Haematologica|August 23, 2006
Heparin- induced thrombocytopenia occurring in the first trimester of pregnancy: successful treatment with lepirudin. A case reportAnna Furlan, Fabrizio Vianello, Maurizio Clementi, et al.
Haematologica|August 23, 2006
Erythrophagocytosis in de novo-philadelphia-positive acute leukemia of ambiguous lineageFrancisco J Ortuño, Cristina Castilla, Maria J Moreno, et al.
Haematologica|August 23, 2006
Successful treatment of refractory angioimmunoblastic T-cell lymphoma with thalidomide and dexamethasoneKarthik Ramasamy, ZiYi Lim, Antonio Pagliuca, et al.
Haematologica|March 15, 2006
Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotypeCornelis L Harteveld, Gerard Steen, L Thomas Vlasveld, et al.
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