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                             32 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Acquired amegakaryocytic thrombocytopenic purpura possibly induced by anti-PD-1 antibody Iyama, Satoshi

99 7 p. 1669-1670
artikel
2 A novel NAP1L4/NUTM1 fusion arising from translocation t(11;15)(p15;q12) in a myeloid neoplasm with eosinophilia and rearrangement of PDGFRA highlights an unusual clinical feature and therapeutic reaction Cheng, Zhao

99 7 p. 1561-1564
artikel
3 Antifungal prophylaxis and novel drugs in acute myeloid leukemia: the midostaurin and posaconazole dilemma Stemler, Jannik

99 7 p. 1429-1440
artikel
4 Autoimmune thrombotic thrombocytopenic purpura (TTP) associated with COVID-19 Albiol, Nil

99 7 p. 1673-1674
artikel
5 Baseline clinical characteristics and disease burden in patients with paroxysmal nocturnal hemoglobinuria (PNH): updated analysis from the International PNH Registry Schrezenmeier, Hubert

99 7 p. 1505-1514
artikel
6 Comparison of central nervous system relapse outcomes following haploidentical vs identical-sibling transplant for acute lymphoblastic leukemia Chen, Qi

99 7 p. 1643-1653
artikel
7 Could ruxolitinib be effective in patients with COVID-19 infection at risk of acute respiratory distress syndrome (ARDS)? Caocci, Giovanni

99 7 p. 1675-1676
artikel
8 COVID-19 infection associated with autoimmune hemolytic anemia Capes, Antoine

99 7 p. 1679-1680
artikel
9 Dynamics of hematopoiesis is disrupted by impaired hematopoietic microenvironment in a mouse model of hemophagocytic lymphohistiocytosis Tsuboi, Isao

99 7 p. 1515-1523
artikel
10 Fifteen years of newborn sickle cell disease screening in Madrid, Spain: an emerging disease in a European country García-Morín, Marina

99 7 p. 1465-1474
artikel
11 Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia Sales, Rahyssa Rodrigues

99 7 p. 1453-1463
artikel
12 Genotypic-phenotypic heterogeneity of δβ-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India Hariharan, Priya

99 7 p. 1475-1483
artikel
13 Geriatric nutritional risk index as a useful prognostic factor in second allogeneic hematopoietic stem cell transplantation Kaito, Satoshi

99 7 p. 1655-1665
artikel
14 Hematological findings in coronavirus disease 2019: indications of progression of disease Liu, Xiaoqing

99 7 p. 1421-1428
artikel
15 Hematological malignancies in Ukraine in post-Chernobyl era: sources of data and their preliminary analysis Koval, Stella V.

99 7 p. 1543-1550
artikel
16 Hodgkin lymphoma-associated hemophagocytic lymphohistiocytosis—a dangerous disease Jin, Zhili

99 7 p. 1575-1581
artikel
17 Immunosuppression therapy is effective for both acquired tumor-associated and primary pure red cell aplasia: a match pair case-control study Chen, Zesong

99 7 p. 1485-1491
artikel
18 Improved time to treatment failure and survival in ibrutinib-treated malignancies with a pharmaceutical care program: an observational cohort study Zerbit, Jeremie

99 7 p. 1615-1625
artikel
19 LPS-induced expression and release of monocyte tissue factor in patients with haemophilia Holstein, Katharina

99 7 p. 1531-1542
artikel
20 Lymphopenia at diagnosis predicts survival of patients with immunodeficiency-associated lymphoproliferative disorders Watanabe, Mizuki

99 7 p. 1565-1573
artikel
21 Modern management of splenomegaly in patients with myelofibrosis Tremblay, Douglas

99 7 p. 1441-1451
artikel
22 Monosomal karyotype and chromosome 17p loss or TP53 mutations in decitabine-treated patients with acute myeloid leukemia Becker, Heiko

99 7 p. 1551-1560
artikel
23 Nationwide study of paroxysmal nocturnal hemoglobinuria in South Korea: paradox of eculizumab Kang, Ka-Won

99 7 p. 1493-1503
artikel
24 Outcome of stem cell transplantation for Waldenström’s macroglobulinemia: analysis of the Japan Society for Hematopoietic Cell Transplantation (JSHCT) Lymphoma Working Group Sakurai, Masatoshi

99 7 p. 1635-1642
artikel
25 Progression of disease within 2 years (POD24) is a clinically relevant endpoint to identify high-risk follicular lymphoma patients in real life Sortais, Clara

99 7 p. 1595-1604
artikel
26 R-CHOP appears to be the best first-line treatment for second primary diffuse large B cell lymphoma: a cancer registry study Systchenko, T.

99 7 p. 1605-1613
artikel
27 Renin angiotensin system inhibitors reduce the incidence of arterial thrombotic events in patients with hypertension and chronic myeloid leukemia treated with second- or third-generation tyrosine kinase inhibitors Mulas, Olga

99 7 p. 1525-1530
artikel
28 Results of R-ESHAP as salvage therapy in refractory/relapsed follicular lymphoma: a real-world experience on behalf of GELCAB group Muntañola, A.

99 7 p. 1627-1634
artikel
29 Safe administration of granulocyte colony-stimulating factor (G-CSF) to a patient with G-CSF–producing multiple myeloma Kikuchi, Taku

99 7 p. 1667-1668
artikel
30 SARS-CoV-2 impact in a community-based hematological ward in an Italian Red Zone Visani, Giuseppe

99 7 p. 1677-1678
artikel
31 The interval between progression and therapy initiation is the key prognostic parameter in relapsing diffuse large B cell lymphoma: analysis from the Czech Lymphoma Study Group database (NIHIL) Janikova, Andrea

99 7 p. 1583-1594
artikel
32 Uterine myeloid sarcoma Martino, Giovanni

99 7 p. 1671-1672
artikel
                             32 gevonden resultaten
 
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