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Results: 1-25 | 26-35
Results: 1-25/35

Authors: Paulussen, M Ahrens, S Dunst, J Winkelmann, W Exner, GU Kotz, R Amann, G Dockhorn-Dworniczak, B Harms, D Muller-Weihrich, S Welte, K Kornhuber, B Janka-Schaub, G Gobel, U Treuner, J Voute, PA Zoubek, A Gadner, H Jurgens, H
Citation: M. Paulussen et al., Localized Ewing tumor of bone: Final results of the cooperative Ewing's Sarcoma Study CESS 86, J CL ONCOL, 19(6), 2001, pp. 1818-1829

Authors: Germeshausen, M Schulze, H Gaudig, A Krukemeier, S Strauss, G Welte, K Ballmaier, M
Citation: M. Germeshausen et al., Congenital Amegakaryocytic thrombocytopenia (CAMT) - a defect of the thrombopoietin receptor c-Mpl, KLIN PADIAT, 213(4), 2001, pp. 155-161

Authors: Lauten, M Stanulla, M Zimmermann, M Welte, K Riehm, H Schrappe, M
Citation: M. Lauten et al., Clinical outcome of patients with childhood acute lymphoblastic leukaemia and an initial leukaemic blood blast count of less than 1000 per microliter, KLIN PADIAT, 213(4), 2001, pp. 169-174

Authors: Beger, C Pierce, LN Kruger, M Marcusson, EG Robbins, JM Welcsh, P Welch, PJ Welte, K King, MC Barber, JR Wong-Staal, F
Citation: C. Beger et al., Identification of Id4 as a regulator of BRCA1 expression by using a ribozyme-library-based inverse genomics approach, P NAS US, 98(1), 2001, pp. 130-135

Authors: Schiller, M Bohm, M Zeidler, C Germeshausen, M Welte, K Luger, TA Bonsmann, G
Citation: M. Schiller et al., Cyclic Neutropenia with mutation in the gene encoding neutrophil elastase (ELA2), HAUTARZT, 52(9), 2001, pp. 790

Authors: Germeshausen, M Schulze, H Ballmaier, M Zeidler, C Welte, K
Citation: M. Germeshausen et al., Mutations in the gene encoding neutrophil elastase (ELA2) are not sufficient to cause the phenotype of congenital neutropenia, BR J HAEM, 115(1), 2001, pp. 222-224

Authors: Tschan, CA Pilz, C Zeidler, C Welte, K Germeshausen, M
Citation: Ca. Tschan et al., Time course of increasing numbers of mutations in the granulocyte colony-stimulating factor receptor gene in a patient with congenital neutropenia who developed leukemia, BLOOD, 97(6), 2001, pp. 1882-1884

Authors: Germeshausen, M Ballmaier, M Schulze, H Welte, K Flohr, T Beiske, K Storm-Mathisen, I Abrahamsen, TG
Citation: M. Germeshausen et al., Granulocyte colony-stimulating factor receptor mutations in a patient withacute lymphoblastic leukemia secondary to severe congenital neutropenia, BLOOD, 97(3), 2001, pp. 829-830

Authors: Ballmaier, M Germeshausen, W Welte, K
Citation: M. Ballmaier et al., Screening for c-mpl mutations in patients with congenital amegakaryocytic thrombocytopenia identities a polymorphism - Response, BLOOD, 97(11), 2001, pp. 3676-3676

Authors: Ballmaier, M Germeshausen, M Schulze, H Cherkaoui, K Lang, S Gaudig, A Krukemeier, S Eilers, M Strauss, G Welte, K
Citation: M. Ballmaier et al., c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia, BLOOD, 97(1), 2001, pp. 139-146

Authors: Anderer, G Schrappe, M Brechlin, AM Lauten, M Muti, P Welte, K Stanulla, M
Citation: G. Anderer et al., Polymorphisms within glutathione S-transferase genes and initial response to glucocorticoids in childhood acute lymphoblastic leukaemia, PHARMACOGEN, 10(8), 2000, pp. 715-726

Authors: Stanulla, M Kasper, B Schrappe, M Viehmann, S Harbott, J Ludwig, WD Welte, K
Citation: M. Stanulla et al., Granulocyte colony-stimulating factor receptor expression and 11q23/MLL genotype in childhood acute lymphoblastic leukemia developing during the first 18 months of life, LEUKEMIA, 14(2), 2000, pp. 337-338

Authors: Schulze, H Ballmaier, M Welte, K Germeshausen, M
Citation: H. Schulze et al., Thrombopoietin induces the generation of distinct Stat1, Stat3, Stat5a andStat5b homo- and heterodimeric complexes with different kinetics in human platelets, EXP HEMATOL, 28(3), 2000, pp. 294-304

Authors: Zeidler, C Schwinzer, B Welte, K
Citation: C. Zeidler et al., Severe congenital neuropenia: Diagnosis and therapy, KLIN PADIAT, 212(4), 2000, pp. 145-152

Authors: Corbacioglu, S Bux, J Konig, A Gabrilove, JL Welte, K Bussel, JB
Citation: S. Corbacioglu et al., Serum granulocyte colony-stimulating factor levels are not increased in patients with autoimmune neutropenia of infancy, J PEDIAT, 137(1), 2000, pp. 96-99

Authors: Mierke, CT Ballmaier, M Werner, U Manns, MP Welte, K Bischoff, SC
Citation: Ct. Mierke et al., Human endothelial cells regulate survival and proliferation of human mast cells, J EXP MED, 192(6), 2000, pp. 801-811

Authors: Cario, G zur Stadt, U Reiter, A Welte, K Sykora, KW
Citation: G. Cario et al., Variant translocations in sporadic Burkitt's lymphoma detected in fresh tumour material: analysis of three cases, BR J HAEM, 110(3), 2000, pp. 537-546

Authors: Zeidler, C Boxer, L Dale, DC Freedman, MH Kinsey, S Welte, K
Citation: C. Zeidler et al., Management of Kostmann syndrome in the G-CSF era, BR J HAEM, 109(3), 2000, pp. 490-495

Authors: Stanulla, M Stumm, M Dieckvoss, BO Seidemann, K Schemmel, V Brechlin, AM Schrappe, M Welte, K Reiter, A
Citation: M. Stanulla et al., No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence, BR J HAEM, 109(1), 2000, pp. 117-120

Authors: Dale, DC Person, RE Bolyard, AA Aprikyan, AG Bos, C Bonilla, MA Boxer, LA Kannourakis, G Zeidler, C Welte, K Benson, KF Horwitz, M
Citation: Dc. Dale et al., Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia, BLOOD, 96(7), 2000, pp. 2317-2322

Authors: Freedman, MH Bonilla, MA Fier, C Bolyard, AA Scarlata, D Boxer, LA Brown, S Cham, B Kannourakis, G Kinsey, SE Mori, PG Cottle, T Welte, K Dale, DC
Citation: Mh. Freedman et al., Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy, BLOOD, 96(2), 2000, pp. 429-436

Authors: Kasper, B Tidow, N Grothues, D Welte, K
Citation: B. Kasper et al., Differential expression and regulation of GTPases (RhoA and Rac2) and GDIs(LyGDI and RhoGDI) in neutrophils from patients with severe congenital neutropenia, BLOOD, 95(9), 2000, pp. 2947-2953

Authors: Zeidler, C Welte, K Barak, Y Barriga, F Bolyard, AA Boxer, L Cornu, G Cowan, MJ Dale, DC Flood, T Freedman, M Gadner, H Mandel, H O'Reilly, RJ Ramenghi, U Reiter, A Skinner, R Vermylen, C Levine, JE
Citation: C. Zeidler et al., Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation, BLOOD, 95(4), 2000, pp. 1195-1198

Authors: Stanulla, M Schrappe, M Brechlin, AM Zimmermann, M Welte, K
Citation: M. Stanulla et al., Polymorphisms within glutathione S-transferase genes (GSTM1, GSTT1, GSTP1)and risk of relapse in childhood B-cell precursor acute lymphoblastic leukemia: a case-control study, BLOOD, 95(4), 2000, pp. 1222-1228

Authors: Schrappe, M Reiter, A Ludwig, WD Harbott, J Zimmermann, M Hiddemann, W Niemeyer, C Henze, G Feldges, A Zintl, F Kornhuber, B Ritter, J Welte, K Gadner, H Riehm, H
Citation: M. Schrappe et al., Improved outcome in childhood acute lymphoblastic leukemia despite reduceduse of anthracyclines and cranial radiotherapy: results of trial ALL-BFM 90, BLOOD, 95(11), 2000, pp. 3310-3322
Risultati: 1-25 | 26-35