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Number of items: 8.

Journal Article

Dietzsch, Stefan, Placzek, Felix, Pietschmann, Klaus, von Bueren, Andre O., Matuschek, Christiane, Glueck, Albrecht, Guckenberger, Matthias, Budach, Volker, Welzel, Jutta, Poettgen, Christoph, Schmidberger, Heinz, Heinzelmann, Frank, Paulsen, Frank, Escudero, Montserrat Pazos, Schwarz, Rudolf, Hornung, Dagmar, Martini, Carmen, Grosu, Anca Ligia, Stueben, Georg, ablonska, Karolina J., Dunst, Juergen, Stranzl-Lawatsch, Heidi, Dieckmann, Karin, Timmermann, Beate, Pietsch, Torsten, Warmuth-Metz, Monika, Bison, Brigitte, Kwiecien, Robert, Benesch, Martin, Gerber, Nicolas U., Grotzer, Michael A., Pfister, Stefan M., Clifford, Steven C., von Hoff, Katja, Klagges, Sabine, Rutkowski, Stefan, Kortmann, Rolf-Dieter and Mynarek, Martin (2020). Evaluation of Prognostic Factors and Role of Participation in a Randomized Trial or a Prospective Registry in Pediatric and Adolescent Nonmetastatic Medulloblastoma - A Report From the HIT 2000 Trial. Adv. Radiat. Oncol., 5 (6). S. 1158 - 1170. SAN DIEGO: ELSEVIER INC. ISSN 2452-1094

Gessi, Marco, von Bueren, Andre O., Treszl, Andras, Muehlen, Anja zur, Hartmann, Wolfgang ORCID: 0000-0002-7609-5021, Warmuth-Metz, Monika, Rutkowski, Stefan and Pietsch, Torsten (2014). MYCN amplification predicts poor outcome for patients with supratentorial primitive neuroectodermal tumors of the central nervous system. Neuro-Oncology, 16 (7). S. 924 - 933. CARY: OXFORD UNIV PRESS INC. ISSN 1523-5866

Gessi, Marco, von Bueren, Andre O., Treszl, Andras, Muehlen, Anja zur, Hartmann, Wolfgang ORCID: 0000-0002-7609-5022, Warmuth-Metz, Monika, Rutkowski, Stefan and Pietsch, Torsten (2014). MYCN amplification predicts poor outcome for patients with supratentorial primitive neuroectodermal tumors of the central nervous system. Neuro-Oncology, 96.575325880677 (4.98385010224095). S. 1329.18259023355 - 1335.94169234138. CARY: OXFORD UNIV PRESS INC. ISSN 1523-5867

Juenger, Stephanie T., Andreiuolo, Felipe, Mynarek, Martin, Doerner, Evelyn, zur Muehlen, Anja, Rutkowski, Stefan, von Bueren, Andre O. and Pietsch, Torsten ORCID: 0000-0003-0763-6506 (2020). Ependymomas in infancy: underlying genetic alterations, histological features, and clinical outcome. Childs Nerv. Syst., 36 (11). S. 2693 - 2701. NEW YORK: SPRINGER. ISSN 1433-0350

Juenger, Stephanie T., Mynarek, Martin, Wohlers, Inken, Doerner, Evelyn, zur Muehlen, Anja, Velez-Char, Natalia, von Hoff, Katja, Rutkowski, Stefan, Warmuth-Metz, Monika, Kortmann, Rolf-Dieter, Timmermann, Beate, Rahmann, Sven, Klein-Hitpass, Ludger, von Bueren, Andre O. and Pietsch, Torsten (2019). Improved risk-stratification for posterior fossa ependymoma of childhood considering clinical, histological and genetic features - a retrospective analysis of the HIT ependymoma trial cohort. Acta Neuropathol. Commun., 7 (1). LONDON: BMC. ISSN 2051-5960

Pfaff, Elke, El Damaty, Ahmed, Balasubramanian, Gnana Prakash, Blattner-Johnson, Mirjam, Worst, Barbara C., Stark, Sebastian, Witt, Hendrik, Pajtler, Kristian W. ORCID: 0000-0002-3562-6121, van Tilburg, Cornelis M., Witt, Ruth, Milde, Till, Jakobs, Martin, Fiesel, Petra, Fruehwald, Michael C., Driever, Pablo Hernaiz, Thomale, Ulrich W., Schuhmann, Martin U., Metzler, Markus, Bochennek, Konrad, Simon, Thorsten, Duerken, Matthias, Karremann, Michael ORCID: 0000-0002-9961-4752, Knirsch, Stephanie, Ebinger, Martin ORCID: 0000-0002-4229-8058, von Bueren, Andre O., Pietsch, Torsten, Herold-Mende, Christel, Reuss, David E., Kiening, Karl, Lichter, Peter, Eggert, Angelika, Kramm, Christof M., Pfister, Stefan M., Jones, David T. W., Baechli, Heidi and Witt, Olaf (2019). Brainstem biopsy in pediatric diffuse intrinsic pontine glioma in the era of precision medicine: the INFORM study experience. Eur. J. Cancer, 114. S. 27 - 36. OXFORD: ELSEVIER SCI LTD. ISSN 1879-0852

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

Worst, Barbara C., van Tilburg, Cornelis M., Balasubramanian, Gnana Prakash, Fiesel, Petra, Witt, Ruth, Freitag, Angelika, Boudalil, Miream, Previti, Christopher, Wolf, Stephan, Schmidt, Sabine, Chotewutmontri, Sasithorn, Bewerunge-Hudler, Melanie, Schick, Matthias, Schlesner, Matthias ORCID: 0000-0002-5896-4086, Hutter, Barbara ORCID: 0000-0002-9034-0329, Taylor, Lenka, Borst, Tobias, Sutter, Christian, Bartram, Claus R., Milde, Till ORCID: 0000-0002-7267-1052, Pfaff, Elke, Kulozik, Andreas E., von Stackelberg, Arend, Meisel, Roland, Borkhardt, Arndt, Reinhardt, Dirk, Klusmann, Jan-Henning ORCID: 0000-0002-1070-0727, Fleischhack, Gudrun, Tippelt, Stephan, Dirksen, Uta, Juergens, Heribert, Kramm, Christof M., von Bueren, Andre O., Westermann, Frank, Fischer, Matthias, Burkhardt, Birgit, Wossmann, Wilhelm, Nathrath, Michaela, Bielack, Stefan S., Fruehwald, Michael C., Fulda, Simone ORCID: 0000-0002-0459-6417, Klingebiel, Thomas, Koscielniak, Ewa, Schwab, Matthias, Tremmel, Roman ORCID: 0000-0003-1564-0433, Driever, Pablo Hernaiz, Schulte, Johannes H., Brors, Benedikt ORCID: 0000-0001-5940-3101, von Deimling, Andreas ORCID: 0000-0002-5863-540X, Lichter, Peter, Eggert, Angelika, Capper, David ORCID: 0000-0003-1945-497X, Pfister, Stefan M., Jones, David T. W. and Witt, Olaf (2016). Next-generation personalised medicine for high-risk paediatric cancer patients - The INFORM pilot study. Eur. J. Cancer, 65. S. 91 - 102. OXFORD: ELSEVIER SCI LTD. ISSN 1879-0852

This list was generated on Tue Oct 19 04:50:39 2021 CEST.