Search Results - "Dreschmann, Verena"

Supratentorial ependymoma in childhood: more than just RELA or YAP by Zschernack, Valentina, Jünger, Stephanie T., Mynarek, Martin, Rutkowski, Stefan, Garre, Maria Luisa, Ebinger, Martin, Neu, Marie, Faber, Jörg, Erdlenbruch, Bernhard, Claviez, Alexander, Bielack, Stefan, Brozou, Triantafyllia, Frühwald, Michael C., Dörner, Evelyn, Dreschmann, Verena, Stock, Annika, Solymosi, Laszlo, Hench, Jürgen, Frank, Stephan, Vokuhl, Christian, Waha, Andreas, Andreiuolo, Felipe, Pietsch, Torsten

“…Two distinct genetically defined entities of ependymoma arising in the supratentorial compartment are characterized by the presence of either a C11orf95-RELA…”
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Type, Frequency, and Spatial Distribution of Immune Cell Infiltrates in CNS Germinomas: Evidence for Inflammatory and Immunosuppressive Mechanisms by Zapka, Pia, Dörner, Evelyn, Dreschmann, Verena, Sakamato, Noriaki, Kristiansen, Glen, Calaminus, Gabriele, Vokuhl, Christian, Leuschner, Ivo, Pietsch, Torsten

“…Abstract Central nervous system germinomas are characterized by a massive immune cell infiltrate. We systematically characterized these immune cells in 28…”
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High frequency of H3F3A K27M mutations characterizes pediatric and adult high-grade gliomas of the spinal cord by Gessi, Marco, Gielen, Gerrit H., Dreschmann, Verena, Waha, Andreas, Pietsch, Torsten

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High frequency of H3F3A (K27M) mutations characterizes pediatric and adult high-grade gliomas of the spinal cord by Gessi, Marco, Gielen, Gerrit H, Dreschmann, Verena, Waha, Andreas, Pietsch, Torsten

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Genomic Alterations of Adamantinomatous and Papillary Craniopharyngioma by Goschzik, Tobias, Gessi, Marco, Dreschmann, Verena, Gebhardt, Ursel, Wang, Linghua, Yamaguchi, Shigeru, Wheeler, David A, Lauriola, Libero, Lau, Ching C, Müller, Hermann L, Pietsch, Torsten

“…Craniopharyngiomas are rare histologically benign but clinically challenging neoplasms. To obtain further information on the molecular genetics and biology of…”
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Supratentorial ependymomas of childhood carry C11orf95–RELA fusions leading to pathological activation of the NF-κB signaling pathway by Pietsch, Torsten, Wohlers, Inken, Goschzik, Tobias, Dreschmann, Verena, Denkhaus, Dorota, Dörner, Evelyn, Rahmann, Sven, Klein-Hitpass, Ludger

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Childhood supratentorial ependymomas with YAP1‐MAMLD1 fusion: an entity with characteristic clinical, radiological, cytogenetic and histopathological features by Andreiuolo, Felipe, Varlet, Pascale, Tauziède‐Espariat, Arnault, Jünger, Stephanie T., Dörner, Evelyn, Dreschmann, Verena, Kuchelmeister, Klaus, Waha, Andreas, Haberler, Christine, Slavc, Irene, Corbacioglu, Selim, Riemenschneider, Markus J., Leipold, Alfred, Rüdiger, Thomas, Körholz, Dieter, Acker, Till, Russo, Alexandra, Faber, Jörg, Sommer, Clemens, Armbrust, Sven, Rose, Martina, Erdlenbruch, Bernhard, Hans, Volkmar H., Bernbeck, Benedikt, Schneider, Dominik, Lorenzen, Johann, Ebinger, Martin, Handgretinger, Rupert, Neumann, Manuela, van Buiren, Miriam, Prinz, Marco, Roganovic, Jelena, Jakovcevic, Antonia, Park, Sung‐Hye, Grill, Jacques, Puget, Stéphanie, Messing‐Jünger, Martina, Reinhard, Harald, Bergmann, Markus, Hattingen, Elke, Pietsch, Torsten

“…Ependymoma with YAP1‐MAMLD1 fusion is a rare, recently described supratentorial neoplasm of childhood, with few cases published so far. We report on 15…”
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Abstract 2853: Comparison of methods for detection of hemispheric gliomas of infancy and their characteristic oncogenic tyrosine kinase gene fusions by Pietsch, Torsten, Gielen, Gerrit, Waha, Andreas, Dörner, Evelyn, Dreschmann, Verena, Kramm, Christof, Vokuhl, Christian

“…Abstract Introduction High grade hemispheric gliomas in infancy (IHG) are characterized by a more favorable outcome compared to high grade gliomas in older…”
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Dysembryoplastic Neuroepithelial Tumor of the Septum Pellucidum and the Supratentorial Midline: Histopathologic, Neuroradiologic, and Molecular Features of 7 Cases by Gessi, Marco, Hattingen, Elke, Dörner, Evelyn, Goschzik, Tobias, Dreschmann, Verena, Waha, Andreas, Pietsch, Torsten

“…Dysembryoplastic neuroepithelial tumors (DNTs) are one of the most common epilepsy-associated low-grade glioneuronal tumors of the central nervous system…”
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Abstract 2492: Identification of RBMS1 in the amplified region 2q24 as a major driver of cellular growth in childhood hepatoblastoma by Rodemann, Martin, Dreschmann, Verena, Dörner, Evelyn, von Schweinitz, Dietrich, Vokuhl, Christian, Pietsch, Torsten

“…Abstract Hepatoblastoma represents the most common primary malignancy of the liver in childhood. Pathological activation of the WNT signaling pathway is…”
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TMIC-47. IMMUNOBIOLOGICAL CHARACTERIZATION OF CNS GERMINOMAS – EVIDENCE FOR INFLAMMATORY AND SUPPRESSIVE IMMUNOLOGICAL MECHANISMS by Zapka, Pia, Doerner, Evelyn, Dreschmann, Verena, Sakamoto, Noriaki, Kristiansen, Glen, Calaminus, Gabriele, Vokuhl, Christian, Leuschner, Ivo, Pietsch, Torsten

“…Germinomas of the CNS are characterized by a massive immune cell infiltrate. Aim of our study was to systematically characterize and quantify these immune…”
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High frequency of H3F3A.sup.K27M mutations characterizes pediatric and adult high-grade gliomas of the spinal cord by Gessi, Marco, Gielen, Gerrit H, Dreschmann, Verena, Waha, Andreas, Pietsch, Torsten

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High frequency of H3F3A ^sup K27M^ mutations characterizes pediatric and adult high-grade gliomas of the spinal cord by Gessi, Marco, Gielen, Gerrit H, Dreschmann, Verena, Waha, Andreas, Pietsch, Torsten

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Intramedullary gangliogliomas: histopathologic and molecular features of 25 cases by Gessi, Marco, MD, Dörner, Evelyn, Dreschmann, Verena, Antonelli, Manila, MD, Waha, Andreas, PhD, Giangaspero, Felice, MD, Gnekow, Astrid, MD, Pietsch, Torsten, MD

“…Summary Gangliogliomas are uncommon glioneuronal tumors, which usually arise in the cerebral hemispheres and occasionally in the brain stem. Gangliogliomas…”
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High-Resolution Genomic Analysis of Cribriform Neuroepithelial Tumors of the Central Nervous System by Gessi, Marco, Japp, Anna Sophia, Dreschmann, Verena, zur Mühlen, Anja, Goschzik, Tobias, Dörner, Evelyn, Pietsch, Torsten

“…Cribriform neuroepithelial tumors (CRINET) are one of several recently characterized entities in the broad spectrum of solid tumors with SMARCB1-INI1 loss…”
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High frequency of H3F3AK27M mutations characterizes pediatric and adult high-grade gliomas of the spinal cord by Gessi, Marco, Gielen, Gerrit H., Dreschmann, Verena, Waha, Andreas, Pietsch, Torsten

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Supratentorial ependymomas of childhood carry C11orf95-RELA fusions leading to pathological activation of the NF-[kappa]B signaling pathway by Pietsch, Torsten, Wohlers, Inken, Goschzik, Tobias, Dreschmann, Verena, Denkhaus, Dorota, Dörner, Evelyn, Rahmann, Sven, Klein-hitpass, Ludger

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