Search Results - Léa Guerrini‐Rousseau

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  1. 1
    ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management

    ERN GENTURIS guidelines on constitutional mismatch repair deficiency diagnosis, genetic counselling, surveillance, quality of life, and clinical management by Chrystelle Colas, Léa Guerrini‐Rousseau, Manon Suerink, Richard Gallon, Christian P. Kratz, Éloïse Ayuso, Laurence Brugières, Katharina Wimmer

    Published 2024
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  2. 2
    Preclinical evaluation of dasatinib alone and in combination with cabozantinib for the treatment of diffuse intrinsic pontine glioma

    Preclinical evaluation of dasatinib alone and in combination with cabozantinib for the treatment of diffuse intrinsic pontine glioma by Nathalène Truffaux, Cathy Philippe, Janna Paulsson, Felipe Andreiuolo, Léa Guerrini‐Rousseau, Gaétan Cornilleau, Ludivine Le Dret, Catherine Richon, Ludovic Lacroix, Stéphanie Puget, Birgit Geoerger, Gilles Vassal, Arne Östman, Jacques Grill

    Published 2014
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  3. 3
    Constitutional mismatch repair deficiency–associated brain tumors: report from the European C4CMMRD consortium

    Constitutional mismatch repair deficiency–associated brain tumors: report from the European C4CMMRD consortium by Léa Guerrini‐Rousseau, Pascale Varlet, Chrystelle Colas, Felipe Andreiuolo, Franck Bourdeaut, Karin Dahan, Christine Devalck, Cécile Faure‐Conter, Maurizio Genuardi, Yael Goldberg, Michaela Kuhlen, Salma Moalla, Enrico Opocher, Vanessa Pérez‐Alonso, Astrid Sehested, Irene Slavc, Sheila Unger, Katharina Wimmer, Jacques Grill, Laurence Brugières

    Published 2019
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  4. 4
    Mesenchymal Transition and PDGFRA Amplification/Mutation Are Key Distinct Oncogenic Events in Pediatric Diffuse Intrinsic Pontine Gliomas

    Mesenchymal Transition and PDGFRA Amplification/Mutation Are Key Distinct Oncogenic Events in Pediatric Diffuse Intrinsic Pontine Gliomas by Stéphanie Puget, Cathy Philippe, Dorine A. Bax, Bastien Job, Pascale Varlet, Marie‐Pierre Junier, Felipe Andreiuolo, Diana Carvalho, Ricardo Reis, Léa Guerrini‐Rousseau, Thomas Roujeau, Philippe Dessen, Catherine Richon, Vladimir Lazar, Gwénaël Le Teuff, Christian Sainte‐Rose, Birgit Geoerger, Gilles Vassal, Chris Jones, Jacques Grill

    Published 2012
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  5. 5
    Germline <i>SUFU</i> mutation carriers and medulloblastoma: clinical characteristics, cancer risk, and prognosis

    Germline <i>SUFU</i> mutation carriers and medulloblastoma: clinical characteristics, cancer risk, and prognosis by Léa Guerrini‐Rousseau, Christelle Dufour, Pascale Varlet, Julien Masliah‐Planchon, Franck Bourdeaut, Marine Guillaud-Bataille, Rachid Abbas, Anne-Isabelle Bertozzi, Fanny Fouyssac, Sophie Huybrechts, Stéphanie Puget, Brigitte Bressac–de Paillerets, Olivier Caron, Nicolas Sévenet, Marina Dimaria, Sophie Villebasse, Olivier Delattre, Dominique Valteau‐Couanet, Jacques Grill, Laurence Brugières

    Published 2017
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  6. 6
    Germline <i>GPR161</i> Mutations Predispose to Pediatric Medulloblastoma

    Germline <i>GPR161</i> Mutations Predispose to Pediatric Medulloblastoma by Matthias Begemann, Sebastian M. Waszak, Giles Robinson, Natalie Jäger, Tanvi Sharma, Cordula Knopp, Florian Kraft, Olga Moser, Martin Mynarek, Léa Guerrini‐Rousseau, Laurence Brugières, Pascale Varlet, Torsten Pietsch, Daniel C. Bowers, Murali Chintagumpala, Felix Sahm, Jan O. Korbel, Stefan Rutkowski, Thomas Eggermann, Amar Gajjar, Paul A. Northcott, Miriam Elbracht, Stefan M. Pfister, Udo Kontny, Ingo Kurth

    Published 2019
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  7. 7
    Prognostic relevance of clinical and molecular risk factors in children with high-risk medulloblastoma treated in the phase II trial PNET HR+5

    Prognostic relevance of clinical and molecular risk factors in children with high-risk medulloblastoma treated in the phase II trial PNET HR+5 by Christelle Dufour, Stéphanie Foulon, Anne Geoffray, Julien Masliah‐Planchon, Dominique Figarella‐Branger, Valérie Bernier‐Chastagner, Laëtitia Padovani, Léa Guerrini‐Rousseau, Cécile Faure‐Conter, Céline Icher, Anne‐Isabelle Bertozzi, Pierre Leblond, Tasnime Akbaraly, Franck Bourdeaut, Nicolás André, Céline Chappé, Pascale Schneider, Émilie De Carli, Pascal Chastagner, Claire Berger, Julien Lejeune, Christine Soler, Natacha Entz‐Werlé, Marie‐Bernadette Delisle

    Published 2020
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  8. 8
    Long-term weight gain in children with craniopharyngioma

    Long-term weight gain in children with craniopharyngioma by Sibylle Rovani, Victoria Butler, Dinane Samara‐Boustani, Graziella Pinto, Laura González-Briceño, Adrien Nguyen Quoc, Gaëlle Vermillac, Athanasia Stoupa, Alix Besançon, Jacques Beltrand, Caroline Thalassinos, Isabelle Flechtner, Yamina Dassa, Magali Viaud, Maria Beatriz Arrom-Branas, Nathalie Boddaert, Stéphanie Puget, Thomas Blauwblomme, Claire Alapetite, Stéphanie Bolle, François Doz, Jacques Grill, Christelle Dufour, Franck Bourdeaut, Samuel Abbou, Léa Guerrini‐Rousseau, Amaury Leruste, Kévin Beccaria, Michel Polak, Dulanjalee Kariyawasam

    Published 2024
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  9. 9
    Supratentorial non-RELA, ZFTA-fused ependymomas: a comprehensive phenotype genotype correlation highlighting the number of zinc fingers in ZFTA-NCOA1/2 fusions

    Supratentorial non-RELA, ZFTA-fused ependymomas: a comprehensive phenotype genotype correlation highlighting the number of zinc fingers in ZFTA-NCOA1/2 fusions by Arnault Tauziède‐Espariat, Aurore Siegfried, Yvan Nicaise, Thomas Kergrohen, Philipp Sievers, Alexandre Vasiljevic, Alexandre Roux, Edouard Dezamis, Chiara Benevello, Marie‐Christine Machet, Sophie Michalak, Chloé Puiseux, Francisco Llamas‐Gutierrez, Pierre Leblond, Franck Bourdeaut, Jacques Grill, Christelle Dufour, Léa Guerrini‐Rousseau, Samuel Abbou, Volodia Dangouloff‐Ros, Nathalie Boddaert, Raphaël Saffroy, Lauren Hasty, Ellen Wahler, Mélanie Pagès, Felipe Andreiuolo, Emmanuèle Lechapt, Fabrice Chrétien, Thomas Blauwblomme, Kévin Beccaria, Johan Pallud, Stéphanie Puget, Emmanuelle Uro‐Coste, Pascale Varlet

    Published 2021
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  10. 10
    Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort

    Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort by Sebastian M. Waszak, Paul A. Northcott, Ivo Buchhalter, Giles Robinson, Christian Sutter, Susanne N. Groebner, Kerstin Grund, Laurence Brugières, David Jones, Kristian W. Pajtler, A. Sorana Morrissy, Marcel Kool, Dominik Sturm, Lukas Chávez, Aurélie Ernst, Sebastian Brabetz, M. Hain, Thomas Zichner, Maia Segura‐Wang, Joachim Weischenfeldt, Tobias Rausch, Balca R. Mardin, Xin Zhou, Cristina Baciu, Christian Lawerenz, Jennifer A. Chan, Pascale Varlet, Léa Guerrini‐Rousseau, Daniel W. Fults, Wiesława Grajkowska, Péter Hauser, Nada Jabado, Young‐Shin Ra, Karel Zitterbart, Suyash Shringarpure, Francisco M. De La Vega, Carlos D. Bustamante, Ho‐Keung Ng, Arie Perry, Tobey J. MacDonald, Pablo Hernáiz Driever, Anne Bendel, Daniel C. Bowers, Geoffrey McCowage, Murali Chintagumpala, Richard J. Cohn, Tim Hassall, Gudrun Fleischhack, Tone Eggen, Finn Wesenberg, Maria Feychting, Birgitta Lannering, Joachim Schüz, Christoffer Johansen, Tina Veje Andersen, Martin Röösli, Claudia E. Kuehni, Michael Grotzer, Kristina Kjærheim, Camelia M. Monoranu, Tenley C. Archer, Elizabeth S. Duke, Scott L. Pomeroy, Shelagh Redmond, Stephan Frank, David Sumerauer, Wolfram Scheurlen, Marina Ryzhova, Till Milde, Christian P. Kratz, David Samuel, Jinghui Zhang, David A. Solomon, Marco A. Marra, Roland Eils, Claus R. Bartram, Katja von Hoff, Stefan Rutkowski, Vijay Ramaswamy, Richard J. Gilbertson, Andrey Korshunov, Michael D. Taylor, Peter Lichter, David Malkin, Amar Gajjar, Jan O. Korbel, Stefan M. Pfister

    Published 2018
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