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                             27 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Analysis of mutational status, SNP rs16754, and expression levels of Wilms tumor 1 (WT1) gene in acute promyelocytic leukemia Gaur, Girish Chander
2012
91 12 p. 1855-1860
artikel
2 Analysis of SNP rs16754 of WT1 gene in a series of de novo acute myeloid leukemia patients Luna, Irene
2012
91 12 p. 1845-1853
artikel
3 A unique pattern of extranodal involvement in Korean adults with sporadic Burkitt lymphoma: a single center experience Jang, Sun-Joo
2012
91 12 p. 1917-1922
artikel
4 CD99 expression and newly diagnosed diffuse large B-cell lymphoma treated with rituximab-CHOP immunochemotherapy Hong, Junshik
2012
91 12 p. 1897-1906
artikel
5 Central nervous system involvement of primary cutaneous diffuse large B cell lymphoma-leg type diagnosed according to the WHO 2008 classification Aoki, Kazunari
2012
91 12 p. 1975-1976
artikel
6 Clinical outcome of treatment with a combined regimen of decitabine and aclacinomycin/cytarabine for patients with refractory acute myeloid leukemia Song, Lu Xi
2012
91 12 p. 1879-1886
artikel
7 Concomitant inhibition of DNA methyltransferase and BCL-2 protein function synergistically induce mitochondrial apoptosis in acute myelogenous leukemia cells Tsao, Twee
2012
91 12 p. 1861-1870
artikel
8 Donor compatibility and performance status affect outcome of allogeneic haematopoietic stem cell transplant in patients with relapsed or refractory acute myeloid leukaemia Damiani, Daniela
2012
91 12 p. 1937-1943
artikel
9 Excellent long-term survival of 170 patients with Waldenström’s macroglobulinemia treated in private oncology practices and a university hospital Hensel, M.
2012
91 12 p. 1923-1928
artikel
10 Fractionated doses of gemtuzumab ozogamicin combined with 3 + 7 induction chemotherapy as salvage treatment for young patients with acute myeloid leukemia in first relapse Malfuson, J. V.
2012
91 12 p. 1871-1877
artikel
11 Frequency and distribution of asymptomatic brain lesions in patients with β-thalassemia intermedia Karimi, Mehran
2012
91 12 p. 1833-1838
artikel
12 Hb Etobicoke mutation in a hybrid HBA212 allele [HBA212 84 (F5) Ser>Arg; HBA212:c.255C>G] Silva, Marcilene Rezende
2012
91 12 p. 1971-1974
artikel
13 Hereditary hemorrhagic telangiectasia patients can tolerate anticoagulation Edwards, Christine Priscilla
2012
91 12 p. 1959-1968
artikel
14 Hypothermic cardiopulmonary bypass surgery in a 7-year-old boy with a cold agglutinin Hubeek, I.
2012
91 12 p. 1989-1990
artikel
15 Large pericardial effusion as a life-threatening complication after hematopoietic stem cell transplantation—association with chronic GVHD in late-onset adult patients Liu, Yao-Chung
2012
91 12 p. 1953-1958
artikel
16 Left and right ventricular function and volume assessment in young thalassemia major patients with no related myocardial iron overload Fernandes, Juliano L.
2012
91 12 p. 1839-1844
artikel
17 NT-pro-BNP: not the prognostic all-rounder in elderly patients undergoing allogeneic stem cell transplantation Haas, Peter S.
2012
91 12 p. 1929-1935
artikel
18 Patients with diffuse large B cell lymphoma in partial response or stable disease after first-line R-CHOP: the prognostic value of the absolute lymphocyte count and impact of autologous stem cell transplantation Hung, Man-Hsin
2012
91 12 p. 1907-1915
artikel
19 Real-world costs of autologous and allogeneic stem cell transplantations for haematological diseases: a multicentre study Blommestein, H. M.
2012
91 12 p. 1945-1952
artikel
20 Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family Kedar, Prabhakar
2012
91 12 p. 1985-1986
artikel
21 Recurrent superior vena cava syndrome caused by IgD multiple myeloma Farnault, L.
2012
91 12 p. 1977-1978
artikel
22 Response to “Severe pernicious anemia with distinct cytogenetic and flow cytometric aberrations mimicking myelodysplastic syndrome” Wells, Denise A.
2012
91 12 p. 1983
artikel
23 Severe pernicious anemia with distinct cytogenetic and flow cytometric aberrations mimicking myelodysplastic syndrome Parmentier, Stefani
2012
91 12 p. 1979-1981
artikel
24 Simultaneous analysis of the expression of 14 genes with individual prognostic value in myelodysplastic syndrome patients at diagnosis: WT1 detection in peripheral blood adversely affects survival Santamaría, Carlos
2012
91 12 p. 1887-1895
artikel
25 Successful cholecystectomy in a patient with aplastic anemia–paroxysmal nocturnal hemoglobinuria during eculizumab treatment Ando, Keiko
2012
91 12 p. 1987-1988
artikel
26 The pharmacokinetic analysis of cyclosporine is essential for the management of refractory pure red cell aplasia Kato, Yuichi
2012
91 12 p. 1991-1992
artikel
27 Thrombotic complications without evidence of hemolysis in paroxysmal nocturnal hemoglobinuria: is eculizumab indicated? Bellido, M.
2012
91 12 p. 1969-1970
artikel
                             27 gevonden resultaten
 
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