Search Results - Maria João Gil‐da‐Costa

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  1. 1
    Metastatic Thyroid Carcinoma Arising from Congenital Goiter due to Mutation in the Thyroperoxidase Gene1

    Metastatic Thyroid Carcinoma Arising from Congenital Goiter due to Mutation in the Thyroperoxidase Gene1 by Geraldo Medeiros‐Neto, Maria João Gil‐da‐Costa, Cecília L. S. Santos, Ana Maria Medina, J. Costa e Silva, Raymond Tsou, Manuel Sobrinho‐Simões

    Published 1998
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  2. 2
    Evaluation of age-dependent treatment strategies for children and young adults with pineoblastoma: analysis of pooled European Society for Paediatric Oncology (SIOP-E) and US Head Start data

    Evaluation of age-dependent treatment strategies for children and young adults with pineoblastoma: analysis of pooled European Society for Paediatric Oncology (SIOP-E) and US Head... by Martin Mynarek, Barry Pizer, Christelle Dufour, Dannis G. van Vuurden, Miklós Garami, Maura Massimino, Jason Fangusaro, Tom B. Davidson, Maria João Gil‐da‐Costa, Jaroslav Štěrba, Martin Benesch, Nicolas U. Gerber, Björn-Ole Juhnke, Robert Kwiecien, Torsten Pietsch, Marcel Kool, Steven C. Clifford, David W. Ellison, Felice Giangaspero, Pieter Wesseling, Floyd H. Gilles, Nicholas G. Gottardo, Jonathan L. Finlay, Stefan Rutkowski, Katja von Hoff

    Published 2016
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  3. 3
    Somatic mutational profiling and clinical impact of driver genes in Latin‐Iberian medulloblastomas: Towards precision medicine

    Somatic mutational profiling and clinical impact of driver genes in Latin‐Iberian medulloblastomas: Towards precision medicine by Letícia Ganem Rillo Paz Barateiro, Rodrigo de Oliveira Cavagna, Mariana Bisarro dos Reis, Flávia Escremim de Paula, Gustavo Ramos Teixeira, Daniel Antunes Moreno, Murilo Bonatelli, Iara Viana Vidigal Santana, Fabiano Pinto Saggioro, Luciano Neder, João Norberto Stávale, Suzana Mária Fleury Malheiros, Hernán Garcı́a Rivello, Silvia Christiansen, Susana Nunes, Maria João Gil da Costa, Jorge Pinheiro, Carlos Almeida Júnior, Bruna Minniti Mançano, Rui Manuel Reis

    Published 2024
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  4. 4
    High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population

    High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population by Daniel Antunes Moreno, Murilo Bonatelli, Augusto Perazzolo Antoniazzi, Flávia Escremim de Paula, Letícia Ferro Leal, Felipe Antônio de Oliveira Garcia, André Escremim de Paula, Gustavo Ramos Teixeira, Iara Viana Vidigal Santana, Fabiano Pinto Saggioro, Luciano Neder, Elvis Terci Valera, Carlos Alberto Scrideli, João Norberto Stávale, Suzana Mária Fleury Malheiros, MATHEUS HENRIQUE ALVES DE LIMA, Glaucia N. M. Hajj, Hernán Garcı́a Rivello, Silvia Christiansen, Susana Nunes, Maria João Gil‐da‐Costa, Jorge Pinheiro, F Martins, Carlos Almeida, Bruna Minniti Mançano, Rui Manuel Reis

    Published 2023
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  5. 5
    Age and DNA methylation subgroup as potential independent risk factors for treatment stratification in children with atypical teratoid/rhabdoid tumors

    Age and DNA methylation subgroup as potential independent risk factors for treatment stratification in children with atypical teratoid/rhabdoid tumors by Michael C. Frühwald, Martin Hasselblatt, Karolina Nemes, Susanne Bens, Mona Steinbügl, Pascal D. Johann, Kornelius Kerl, Péter Hauser, Eduardo Quiroga, Palma Solano‐Páez, Veronica Biassoni, Maria João Gil‐da‐Costa, Martha Perek-Polnik, Marianne D. van de Wetering, David Sumerauer, Jane Pears, Niklas Stabell, Stefan Holm, Heinz Hengartner, Nicolas U. Gerber, Michael Grotzer, Joachim Boos, Martin Ebinger, Stefan Tippelt, Werner Paulus, Rhoikos Furtwängler, Pablo Hernáiz Driever, Harald Reinhard, Stefan Rutkowski, Paul‐Gerhardt Schlegel, Irene Schmid, Rolf‐Dieter Kortmann, Beate Timmermann, Monika Warmuth‐Metz, Uwe Kordes, Joachim Gerß, Karsten Nysom, Reinhard Schneppenheim, Reiner Siebert, Marcel Kool, Norbert Graf

    Published 2019
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  6. 6
    Diagnostics and treatment of diffuse intrinsic pontine glioma: where do we stand?

    Diagnostics and treatment of diffuse intrinsic pontine glioma: where do we stand? by Fatma E. El‐Khouly, Sophie E. M. Veldhuijzen van Zanten, Vicente Santa‐María López, N. Harry Hendrikse, Gertjan J.L. Kaspers, G. Loizos, David Sumerauer, Karsten Nysom, Kaie Pruunsild, Virve Pentikäinen, Halldora K. Thorarinsdottir, Giedrė Rutkauskienė, Victor Calvagna, Monika Drogosiewicz, Monica Dragomir, Ladislav Deak, Lidija Kitanovski, André O. von Bueren, Rejin Kebudi, Irene Slavc, Sandra Jacobs, Filip Jadrijević-Cvrlje, Natacha Entz‐Werlé, Jacques Grill, Antonis Kattamis, Péter Hauser, Jane Pears, Veronica Biassoni, Maura Massimino, Enrique López Aguilar, Ingrid Kristin Torsvik, Maria João Gil‐da‐Costa, Э. В. Кумирова, Ofelia Cruz, Stefan Holm, Simon Bailey, Tim Hayden, Ulrich W. Thomale, Geert O. Janssens, Christof M. Kramm, Dannis G. van Vuurden

    Published 2019
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  7. 7
    NFB-13. Rhabdoid Tumor Predisposition Syndrome (RTPS) – Finding Evidence by systematic Analyses

    NFB-13. Rhabdoid Tumor Predisposition Syndrome (RTPS) – Finding Evidence by systematic Analyses by Karolina Nemes, Susanne Bens, Pascal D. Johann, Mona Steinbügl, Miriam Gruhle, Denis Kachanov, M. V. Teleshova, Péter Hauser, Thorsten Simon, Stephan Tippelt, W. Eberl, Wilhelm Woessmann, Christian P. Kratz, Floor Abbink, Pablo Hernáiz Driever, Matthias Eyrich, David Sumerauer, Till Milde, Harald Reinhard, Alfred Leipold, Marianne D. van de Wetering, Maria João Gil‐da‐Costa, Georg Ebetsberger‐Dachs, Carmen Hernández Marqúes, Nina Bauer, Veronica Biassoni, Clarice Franco Meneses, Stephanie Knirsch, Melchior Lauten, Nicolas U. Gerber, Martin Chada, Kornelius Kerl, Andreas Lemmer, Heidrun Boztug, Michaela Kuhlen, Rhoikos Furtwängler, Uwe Kordes, Reiner Schneppenheim, Christian Vokuhl, Martin Hasselblatt, Thomas Kröncke, Brigitte Bison, Patrick Melchior, Beate Timmermann, Joachim Gerß, Reiner Siebert, Michael C. Frühwald

    Published 2022
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  8. 8
    Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study

    Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study by Katja von Hoff, Christine Haberler, Felix Schmitt-Hoffner, Elizabeth Schepke, Teresa de Rojas, Sandra Jacobs, Michal Zápotocký, David Sumerauer, Marta Perek‐Polnik, Christelle Dufour, Dannis G. van Vuurden, Irene Slavc, Johannes Gojo, Jessica C. Pickles, Nicolas U. Gerber, Maura Massimino, Maria João Gil‐da‐Costa, Miklós Garami, Э. В. Кумирова, Astrid Sehested, David Scheie, Ofelia Cruz, Lucas Moreno, Jaeho Cho, Bernward Zeller, Niels Bovenschen, Michael Grotzer, Daniel Alderete, Matija Snuderl, Olga Zheludkova, Andrey Golanov, Konstantin Okonechnikov, Martin Mynarek, Björn Ole Juhnke, Stefan Rutkowski, Ulrich Schüller, Barry Pizer, Barbara von Zezschwitz, Robert Kwiecien, Maximilian Wechsung, Frank Konietschke, Eugene I. Hwang, Dominik Sturm, Stefan M. Pfister, Andreas von Deimling, Elisabeth J. Rushing, Marina Ryzhova, Péter Hauser, Maria Łastowska, Pieter Wesseling, Felice Giangaspero, Cynthia Hawkins, Dominique Figarella-Branger, Charles G. Eberhart, Peter C. Burger, Marco Gessi, Andrey Korshunov, Tom Jacques, David Capper, Torsten Pietsch, Marcel Kool

    Published 2021
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  9. 9
    Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas

    Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas by Ana Guerreiro Stücklin, Scott Ryall, Kohei Fukuoka, Michal Zápotocký, Álvaro Lassaletta, Christopher Li, Taylor Bridge, Byungjin Kim, Anthony Arnoldo, Paul E. Kowalski, Yunan Zhong, Monique Johnson, Claire Li, Arun Ramani, Robert Siddaway, Liana Nobre, Pasqualino de Antonellis, Christopher Dunham, Sylvia Cheng, Daniel R. Boué, Jonathan L. Finlay, Scott Coven, Inmaculada de Prada, Marta Pérez‐Somarriba, Cláudia C. Faria, Michael Grotzer, Elisabeth J. Rushing, David Sumerauer, Josef Zámečnı́k, Lenka Krsková, Miguel García-Ariza, Ofelia Cruz, Andrés Morales La Madrid, Palma Solano‐Páez, Keita Terashima, Yoshiko Nakano, Koichi Ichimura, Motoo Nagane, Hiroaki Sakamoto, Maria João Gil‐da‐Costa, Roberto Silva, Donna L. Johnston, Jean Michaud, Bev Wilson, Frank K.H. van Landeghem, Angélica Oviedo, P. Daniel McNeely, Bruce Crooks, Iris Fried, Nataliya Zhukova, Jordan R. Hansford, Amulya NageswaraRao, Livia Garzia, Mary Shago, Michael Brudno, Meredith S. Irwin, Ute Bartels, Vijay Ramaswamy, Éric Bouffet, Michael D. Taylor, Uri Tabori, Cynthia Hawkins

    Published 2019
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  10. 10
    The molecular landscape of ETMR at diagnosis and relapse

    The molecular landscape of ETMR at diagnosis and relapse by Sander Lambo, Susanne Gröbner, Tobias Rausch, Sebastian M. Waszak, Christin Schmidt, Aparna Gorthi, July Carolina Romero, Monika Mauermann, Sebastian Brabetz, Sonja Krausert, Ivo Buchhalter, Jan Köster, Danny A. Zwijnenburg, Martin Sill, Jens-Martin Hübner, Norman Mack, Benjamin Schwalm, Marina Ryzhova, Volker Hovestadt, Simon Papillon‐Cavanagh, Jennifer A. Chan, Pablo Landgraf, Ben Ho, Till Milde, Olaf Witt, Jonas Ecker, Felix Sahm, David Sumerauer, David W. Ellison, Brent A. Orr, Anna Darabi, Christine Haberler, Dominique Figarella‐Branger, Pieter Wesseling, Jens Schittenhelm, Marc Remke, Michael D. Taylor, Maria João Gil‐da‐Costa, Maria Łastowska, Wiesława Grajkowska, Martin Hasselblatt, Péter Hauser, Torsten Pietsch, Emmanuelle Uro‐Coste, Franck Bourdeaut, Julien Masliah‐Planchon, Valérie Rigau, Sanda Alexandrescu, Stephan Wolf, Xiao-Nan Li, Ulrich Schüller, Matija Snuderl, Matthias A. Karajannis, Felice Giangaspero, Nada Jabado, Andreas von Deimling, David Jones, Jan Korbel, Katja von Hoff, Peter Lichter, Annie Huang, Alexander J. R. Bishop, Stefan M. Pfister, Andrey Korshunov, Marcel Kool

    Published 2019
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  11. 11
    Development of the SIOPE DIPG network, registry and imaging repository: a collaborative effort to optimize research into a rare and lethal disease

    Development of the SIOPE DIPG network, registry and imaging repository: a collaborative effort to optimize research into a rare and lethal disease by Sophie E. M. Veldhuijzen van Zanten, Joshua Baugh, Brooklyn Chaney, Dennis de Jongh, Esther Sánchez Aliaga, Frederik Barkhof, Johan Noltes, Ruben De Wolf, Jet Van Dijk, Antonio Cannarozzo, Carin M. Damen-Korbijn, Jan A. Lieverst, Niclas Colditz, Marion Hoffmann, Monika Warmuth‐Metz, Brigitte Bison, David Jones, Dominik Sturm, Gerrit H. Gielen, Chris Jones, Esther Hulleman, Raphaël Calmon, David Castel, Pascale Varlet, G Giraud, Irene Slavc, Stefaan Van Gool, Sandra Jacobs, Filip Jadrijević-Cvrlje, David Sumerauer, Karsten Nysom, Virve Pentikäinen, Sanna‐Maria Kivivuori, Pierre Leblond, Natasha Entz-Werle, André O. von Bueren, Antonis Kattamis, Darren Hargrave, Péter Hauser, Miklós Garami, Halldora K. Thorarinsdottir, Jane Pears, Lorenza Gandola, Giedrė Rutkauskienė, Geert O. Janssens, Ingrid Kristin Torsvik, Marta Perek‐Polnik, Maria João Gil‐da‐Costa, Olga Zheludkova, Л. И. Шац, Ladislav Deak, Lidija Kitanovski, Ofelia Cruz, Andrés Morales La Madrid, Stefan Holm, Nicolas U. Gerber, Rejin Kebudi, Richard G. Grundy, Enrique López‐Aguilar, Marta Zapata‐Tarrés, John Emmerik, Tim Hayden, Simon Bailey, Veronica Biassoni, Maura Massimino, Jacques Grill, W. Peter Vandertop, Gertjan J.L. Kaspers, Maryam Fouladi, Christof M. Kramm, Dannis G. van Vuurden

    Published 2017
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