Search Results - "Frühwald, Michael Christoph"

Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor by Kordes, Uwe, Gesk, Stefan, Frühwald, Michael Christoph, Graf, Norbert, Leuschner, Ivo, Hasselblatt, Martin, Jeibmann, Astrid, Oyen, Florian, Peters, Ove, Pietsch, Torsten, Siebert, Reiner, Schneppenheim, Reinhard

“…The SMARCB1 gene status in 50 patients with atypical teratoid rhabdoid tumor and/or malignant rhabdoid tumor recruited to a German registry was prospectively…”
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Improved 6‐year overall survival in AT/RT – results of the registry study Rhabdoid 2007 by Bartelheim, Kerstin, Nemes, Karolina, Seeringer, Angela, Kerl, Kornelius, Buechner, Jochen, Boos, Joachim, Graf, Norbert, Dürken, Matthias, Gerss, Joachim, Hasselblatt, Martin, Kortmann, Rolf‐Dieter, Teichert von Luettichau, Irene, Nagel, Inga, Nygaard, Randi, Oyen, Florian, Quiroga, Eduardo, Schlegel, Paul‐Gerhardt, Schmid, Irene, Schneppenheim, Reinhard, Siebert, Reiner, Solano‐Paez, Palma, Timmermann, Beate, Warmuth‐Metz, Monika, Frühwald, Michael Christoph

“…Atypical teratoid rhabdoid tumors (AT/RT) are characterized by mutations and subsequent inactivation of SMARCB1 (INI1, hSNF5), a predilection for very young…”
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The extraordinary challenge of treating patients with congenital rhabdoid tumors—a collaborative European effort by Nemes, Karolina, Clément, Nathalie, Kachanov, Denis, Bens, Susanne, Hasselblatt, Martin, Timmermann, Beate, Schneppenheim, Reinhard, Gerss, Joachim, Siebert, Reiner, Furtwängler, Rhoikos, Bourdeaut, Franck, Frühwald, Michael Christoph, Zlatic, Monica, Shamanskaya, Tatyana, Varfolomeeva, Svetlana, Kerl, Kornelius, Abbink, Floor, Ebinger, Martin, Tippelt, Stephan, Graf, Norbert, Hernáiz‐Driever, Pablo, Gil‐Da‐Costa, Maria João, Klingebiel, Thomas, Kortmann, Rolf‐Dieter, Pears, Jane, Schlegel, Paul‐Gerhardt, Andre, Nicolas, Bertozzi, Anne‐Isabelle, Corradini, Nadège, Dufour, Christelle, Fouyssac, Fanny, Leblond, Pierre, Delattre, Olivier, Masliah‐Planchon, Julien, Simon, Thorsten, Witt, Olaf

“…Background Congenital rhabdoid tumors are rare and highly aggressive malignancies. In general, patients are considered to be incurable and are often treated…”
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ATRT-17. ASSISTED REPRODUCTIVE TECHNOLOGIES AND THE DEVELOPMENT OF MALIGNANT RHABDOID TUMOURS by Nemes, Karolina, Hasselblatt, Martin, Bens, Susanne, Erdreich-Epstein, Anat, Biegel, Jaclyn, Khatib, Ziad, Liaugaudiene, Olga, Sadeghipour, Alireza, Ebetsberger-Dachs, Georg, Lemmer, Andreas, Khurana, Claudia, von der Weid, Nicolas, Schmid, Irene, Mora, Jaume, Marques, Carmen Hernandez, Pears, Jane, Timmermann, Beate, Kodes, Uwe, Gerss, Joachim, Furtwängler, Rhoikos, Siebert, Reiner, Frühwald, Michael Christoph

“…Abstract As the pathogenesis of rhabdoid tumors (RT) relies on epigenetic disturbances a potential link to assisted reproductive technologies (ART) deserves…”
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Medulloblastoma: A developmental abnormality of the cerebellum. A comprehensive analysis of genetic and epigenetic alterations by Fruhwald, Michael Christoph

“…Medulloblastomas are the most common malignant tumors of the CNS in children. The propensity of these malignancies to arise from the developing cerebellum…”
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