Items where Author or Editor is "Goehring, Gudrun" - Kölner UniversitätsPublikationsServer

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Number of items: 6.

Journal Article

Koenecke, Christian ORCID: 0000-0001-7025-1735, Goehring, Gudrun, de Wreede, Liesbeth C., van Biezen, Anja, Scheid, Christof, Volin, Liisa ORCID: 0000-0002-9731-8335, Maertens, Johan, Finke, Juergen, Schaap, Nicolaas ORCID: 0000-0001-7696-4752, Robin, Marie ORCID: 0000-0003-1388-9876, Passweg, Jakob, Cornelissen, Jan, Beelen, Dietrich ORCID: 0000-0001-5050-220X, Heuser, Michael ORCID: 0000-0001-5318-9044, de Witte, Theo and Kroeger, Nicolaus (2015). Impact of the revised International Prognostic Scoring System, cytogenetics and monosomal karyotype on outcome after allogeneic stem cell transplantation for myelodysplastic syndromes and secondary acute myeloid leukemia evolving from myelodysplastic syndromes: a retrospective multicenter study of the European Society of Blood and Marrow Transplantation. Haematologica, 100 (3). S. 400 - 409. PAVIA: FERRATA STORTI FOUNDATION. ISSN 0390-6078

Ripperger, Tim ORCID: 0000-0001-6470-8612, Bielack, Stefan S., Borkhardt, Arndt, Brecht, Ines B., Burkhardt, Birgit, Calaminus, Gabriele, Debatin, Klaus-Michael ORCID: 0000-0002-8397-1886, Deubzer, Hedwig, Dirksen, Uta, Eckert, Cornelia, Eggert, Angelika, Erlacher, Miriam, Fleischhack, Gudrun, Fruehwald, Michael C., Gnekow, Astrid, Goehring, Gudrun, Graf, Norbert ORCID: 0000-0002-2248-323X, Hanenberg, Helmut, Hauer, Julia, Hero, Barbara, Hettmer, Simone, von Hoff, Katja, Horstmann, Martin, Hoyer, Juliane, Illig, Thomas, Kaatsch, Peter, Kappler, Roland ORCID: 0000-0002-8581-2803, Kerl, Kornelius, Klingebiel, Thomas, Kontny, Udo, Kordes, Uwe ORCID: 0000-0001-6375-2320, Koerholz, Dieter, Koscielniak, Ewa, Kramm, Christof M., Kuhlen, Michaela, Kulozik, Andreas E., Lamottke, Britta, Leuschner, Ivo, Lohmann, Dietmar R. ORCID: 0000-0002-2624-9889, Meinhardt, Andrea, Metzler, Markus ORCID: 0000-0002-4523-1676, Meyer, Lder H., Moser, Olga, Nathrath, Michaela, Niemeyer, Charlotte M., Nustede, Rainer, Pajtler, Kristian W. ORCID: 0000-0002-3562-6121, Paret, Claudia ORCID: 0000-0002-9094-1634, Rasche, Mareike, Reinhardt, Dirk, Riess, Olaf, Russo, Alexandra, Rutkowski, Stefan, Schlegelberger, Brigitte, Schneider, Dominik, Schneppenheim, Reinhard, Schrappe, Martin, Schroeder, Christopher, von Schweinitz, Dietrich, Simon, Thorsten, Sparber-Sauer, Monika, Spix, Claudia, Stanulla, Martin ORCID: 0000-0002-3834-0727, Steinemann, Doris, Strahm, Brigitte, Temming, Petra, Thomay, Kathrin, von Bueren, Andre O., Vorwerk, Peter, Witt, Olaf, Wlodarski, Marcin, Woessmann, Willy, Zenker, Martin, Zimmermann, Stefanie, Pfister, Stefan M. and Kratz, Christian P. (2017). Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology. Am. J. Med. Genet. A, 173 (4). S. 1017 - 1038. HOBOKEN: WILEY. ISSN 1552-4833

Speckmann, Carsten ORCID: 0000-0002-6217-1556, Sahoo, Sushree Sangita, Rizzi, Marta, Hirabayashi, Shinsuke, Karow, Axel, Serwas, Nina Kathrin, Hoemberg, Marc, Damatova, Natalja, Schindler, Detlev, Vannier, Jean-Baptiste, Boulton, Simon J., Pannicke, Ulrich, Goehring, Gudrun, Thomay, Kathrin, Verdu-Amoros, J. J., Hauch, Holger, Woessmann, Wilhelm, Escherich, Gabriele, Laack, Eckart, Rindle, Liliana, Seidl, Maximilian, Rensing-Ehl, Anne, Lausch, Ekkehart, Jandrasits, Christine, Strahm, Brigitte, Schwarz, Klaus, Ehl, Stephan R., Niemeyer, Charlotte, Boztug, Kaan ORCID: 0000-0001-8387-9185 and Wlodarski, Marcin W. (2017). Clinical and Molecular Heterogeneity of RTE L1 Deficiency (vol 8, pg 449, 2017). Front. Immunol., 8. LAUSANNE: FRONTIERS MEDIA SA. ISSN 1664-3224

Speckmann, Carsten ORCID: 0000-0002-6217-1556, Sahoo, Sushree Sangita, Rizzi, Marta, Hirabayashi, Shinsuke, Karow, Axel, Serwas, Nina Kathrin, Hoemberg, Marc, Damatova, Natalja, Schindler, Detlev, Vannier, Jean-Baptiste, Boulton, Simon J., Pannicke, Ulrich, Goehring, Gudrun, Thomay, Kathrin, Verdu-Amoros, J. J., Hauch, Holger, Woessmann, Wilhelm, Escherich, Gabriele, Laack, Eckart, Rindle, Liliana, Seidl, Maximilian, Rensing-Ehl, Anne, Lausch, Ekkehart, Jandrasits, Christine ORCID: 0000-0003-1357-4401, Strahm, Brigitte, Schwarz, Klaus, Ehl, Stephan R., Niemeyer, Charlotte, Boztug, Kaan ORCID: 0000-0001-8387-9185 and Wlodarski, Marcin W. (2017). Clinical and Molecular Heterogeneity of RTEL1 Deficiency. Front. Immunol., 8. LAUSANNE: FRONTIERS MEDIA SA. ISSN 1664-3224

Suttorp, Meinolf, Schulze, Philipp, Glauche, Ingmar, Goehring, Gudrun, von Neuhoff, Nils, Metzler, Markus, Sedlacek, Petr, de Bont, Eveline S. J. M., Balduzzi, Adriana, Lausen, Birgitte, Aleinikova, Olga, Sufliarska, Sabina, Henze, Guenter, Strauss, Gabriele, Eggert, Angelika, Kremens, Bernhard, Groll, Andreas H., Berthold, Frank, Klein, Christoph, Gross-Wieltsch, Ute, Sykora, Karl Walter, Borkhardt, Arndt, Kulozik, Andreas E., Schrappe, Martin, Nowasz, Christina, Krumbholz, Manuela, Tauer, Josephine T. ORCID: 0000-0002-6079-4653, Claviez, Alexander, Harbott, Jochen, Kreipe, Hans H., Schlegelberger, Brigitte and Thiede, Christian (2018). Front-line imatinib treatment in children and adolescents with chronic myeloid leukemia: results from a phase III trial. Leukemia, 32 (7). S. 1657 - 1670. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5551

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