| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A CD33-specific single-chain immunotoxin mediates potent apoptosis of cultured human myeloid leukaemia cells
|
Schwemmlein, Michael
|
|
2006
|
133 |
2 |
p. 141-151
|
artikel
|
| 2 |
A century of Auer's rods
|
|
|
2006
|
133 |
2 |
p. 111
|
artikel
|
| 3 |
Allogeneic haematopoietic stem cell transplantation in relapsed or refractory anaplastic large cell lymphoma of children and adolescents – a Berlin–Frankfurt–Münster group report
|
Woessmann, Willi
|
|
2006
|
133 |
2 |
p. 176-182
|
artikel
|
| 4 |
An unusual case of indigestion: persistence of phagocytosed Auer rods in acute promyelocytic leukaemia
|
|
|
2006
|
133 |
2 |
p. 112
|
artikel
|
| 5 |
Aspirin use in myeloma: a note of caution regarding potential tumour necrosis factor-alpha elevation
|
|
|
2006
|
133 |
2 |
p. 216
|
artikel
|
| 6 |
Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotype
|
Worth, Austen
|
|
2006
|
133 |
2 |
p. 124-140
|
artikel
|
| 7 |
Circulating levels and clinical significance of soluble CD86 in myeloma patients
|
Hock, B. D.
|
|
2006
|
133 |
2 |
p. 165-172
|
artikel
|
| 8 |
Co-inheritance of α+-thalassaemia and sickle trait results in specific effects on haematological parameters
|
Wambua, Sammy
|
|
2006
|
133 |
2 |
p. 206-209
|
artikel
|
| 9 |
Delayed diagnosis and complications of Fanconi anaemia at advanced age – a paradigm
|
Huck, Kirsten
|
|
2006
|
133 |
2 |
p. 188-197
|
artikel
|
| 10 |
Hereditary pyrimidine 5′-nucleotidase deficiency: from genetics to clinical manifestations
|
Zanella, Alberto
|
|
2006
|
133 |
2 |
p. 113-123
|
artikel
|
| 11 |
High incidence of myelodysplasia and secondary leukaemia in the UK Medical Research Council Pilot of autografting in chronic lymphocytic leukaemia
|
Milligan, Donald W.
|
|
2006
|
133 |
2 |
p. 173-175
|
artikel
|
| 12 |
Papers to be published in forthcoming issues
|
|
|
2006
|
133 |
2 |
p. x
|
artikel
|
| 13 |
Phase I/II study of vaccination with dendritic-like leukaemia cells for the immunotherapy of acute myeloid leukaemia
|
Roddie, H.
|
|
2006
|
133 |
2 |
p. 152-157
|
artikel
|
| 14 |
Positron emission tomography scans for distinguishing between osteomyelitis and infarction in sickle cell disease
|
|
|
2006
|
133 |
2 |
p. 212-214
|
artikel
|
| 15 |
Prognostic model for disease-specific and overall mortality in newly diagnosed symptomatic patients with Waldenstrom macroglobulinaemia
|
Ghobrial, Irene M.
|
|
2006
|
133 |
2 |
p. 158-164
|
artikel
|
| 16 |
Stroke may appear to be rare in Saudi-Arabian and Nigerian children with sickle cell disease, but not in Cameroonian sickle cell patients
|
|
|
2006
|
133 |
2 |
p. 210
|
artikel
|
| 17 |
Stroke may appear to be rare in Saudi-Arabian and Nigerian children with sickle cell disease, but not in Cameroonian sickle cell patients – response to Njamnshi et al
|
|
|
2006
|
133 |
2 |
p. 211
|
artikel
|
| 18 |
Temporal development of myeloma in a syngeneic twin pair
|
|
|
2006
|
133 |
2 |
p. 211-212
|
artikel
|
| 19 |
The c.−1639G > A polymorphism of the VKORC1 gene is a major determinant of the response to acenocoumarol in anticoagulated patients
|
Montes, Ramón
|
|
2006
|
133 |
2 |
p. 183-187
|
artikel
|
| 20 |
The use of rituximab in two children with allo-antibodies towards factor VIII
|
|
|
2006
|
133 |
2 |
p. 214-216
|
artikel
|
| 21 |
Use of the oral chelator deferiprone in the treatment of iron overload in patients with Hb H disease
|
Chan, Joyce C. W.
|
|
2006
|
133 |
2 |
p. 198-205
|
artikel
|
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