Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Lea Guerrini-Rousseau"'
Autor:
Daniel Orbach, Ines B. Brecht, Nadege Corradini, Yassine Bouchoucha, Jelena Roganovic, Franck Bourdeaut, Yves Reguerre, Roland P. Kuiper, Brigitte Bressac de Paillerets, Andrea Ferrari, Calogero Virgone, Jan Godzinski, Gianni Bisogno, Lea Guerrini-Rousseau, Nuno Jorge Farinha, Luca Bergamaschi, Ewa Bien, Michaela Kuhlen, Dominik T. Schneider, Tal Ben Ami
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100023- (2023)
Germline predisposing pathogenic variants (GPVs) are present in approximately 8–10 % of children with all cancer types. Very rare tumours (VRTs) represent many different diseases, defined with an annual incidence
Externí odkaz:
https://doaj.org/article/d62e20c9c6424c0bb4631c4a7f0fd964
Autor:
Stephanie Puget, Cathy Philippe, Dorine A Bax, Bastien Job, Pascale Varlet, Marie-Pierre Junier, Felipe Andreiuolo, Dina Carvalho, Ricardo Reis, Lea Guerrini-Rousseau, Thomas Roujeau, Philippe Dessen, Catherine Richon, Vladimir Lazar, Gwenael Le Teuff, Christian Sainte-Rose, Birgit Geoerger, Gilles Vassal, Chris Jones, Jacques Grill
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e30313 (2012)
Diffuse intrinsic pontine glioma (DIPG) is one of the most frequent malignant pediatric brain tumor and its prognosis is universaly fatal. No significant improvement has been made in last thirty years over the standard treatment with radiotherapy. To
Externí odkaz:
https://doaj.org/article/6e75a25c66ea440bbeecf2bc0985720c
Autor:
Magali Raveneau, Volodia Dangouloff-Ross, Charles-Joris Roux, Raphael Levy, Lea Guerrini-Rousseau, Annick Sevely, Jean Darcourt, Fabrice Bonneville, Nathalie Boddaert
Publikováno v:
Journal of Neuroradiology. 50:130-131
Autor:
Anna Kolodziejczak, Lea Guerrini-Rousseau, Julien Masliah Planchon, Jonas Ecker, Florian Selt, Martin Mynarek, Denise Obrecht, Martin Sill, Steffen Hirsch, Dominik Sturm, Sebastian M Waszak, Vijay Ramaswamy, Virve Pentikainen, Haci Ahmet Demir, Steven C Clifford, Ed Schwalbe, Luca Massimi, Matija Snuderl, Kristyn Galbraith, Matthias A Karajannis, Katie Hill, Bryan Li, Christine L White, Shelagh Redmond, Loizou Loizos, Marcus Jakob, Uwe Kordes, Irene Schmid, Julia Hauer, Claudia Blattmann, Maria Filippidou, Wolfram Scheurlen, Udo Kontny, Kerstin Grund, Christian Sutter, Torsten Pietsch, Cornelis M van Tilburg, Stephan Frank, Denis M Schewe, David Malkin, Michael D Taylor, Uri Tabori, Eric Bouffet, Marcel Kool, Felix Sahm, Andreas von Deimling, Andrey Korshunov, Katja Von Hoff, Christian Kratz, David T W Jones, Stefan Rutkowski, Olaf Witt, Gaelle Bougeard, Kristian W Pajtler, Stefan M Pfister, Franck Bourdeaut, Till Milde
PURPOSE: The prognosis for SHH-medulloblastoma (MB) patients with Li-Fraumeni syndrome (LFS) is poor. Due to lack of comprehensive data for these patients, it is challenging to establish effective therapeutic recommendations. We here describe the lar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15469ae7e19a9bc211d9763086a10d58
https://nrl.northumbria.ac.uk/id/eprint/49500/1/noac079.389.pdf
https://nrl.northumbria.ac.uk/id/eprint/49500/1/noac079.389.pdf
Autor:
Lea Guerrini-Rousseau, Odile Cabaret, Martine Muleris, Dominique Vidaud, Sophie Cotteret, Etienne Rouleau, Tiphaine Adam de Beaumais, Pascale Varlet, Raphael Morscher, Samuel Abbou, Christelle Dufour, Laurence Brugieres, Jacques Grill
Publikováno v:
Neuro-Oncology. 24:i69-i70
Constitutional Mismatch Repair Deficiency (CMMRD) and Neurofibromatosis type 1 (NF1) are brain tumor predisposing syndromes associated with café-au-lait macules (CALM). Due to this overlap, establishing the differential diagnosis can be difficult, b
Autor:
Lea Guerrini-Rousseau, Jane Merlevede, Philippe Denizeau, Felipe Andrejuolo, Pascale Varlet, Stephanie Puget, Kevin Beccaria, Thomas Blauwblomme, Odile Cabaret, Nadim Hamzaoui, Franck Bourdeaut, Cecile Faure-Conter, Martine Muleris, Chrystelle Colas, Tiphaine Adam de Beaumais, David Castel, Etienne Rouleau, Laurence Brugieres, Jacques Grill, Marie-Anne Debily
Publikováno v:
Neuro-Oncology. 24:i70-i70
PURPOSE: Constitutional Mismatch Repair Deficiency (CMMRD) is a cancer predisposition due to bi-allelic mutations in one of the four main mismatch repair (MMR) genes (PMS2, MSH2, MSH6 or MLH1) associated with early onset of cancers, especially gliobl
Autor:
Lea Guerrini-Rousseau, Pauline Hoarau, Gaelle Bougeard, Lisa Golmard, Chrystelle Colas, Marion Gauthier-Villars, Claude Houdayer, Thierry Frebourg, Franck Bourdeaut, Laurence Brugieres
Publikováno v:
Neuro-Oncology. 24:i47-i47
A pathogenic or likely pathogenic variant (PV) in a major cancer predisposition gene is identified in almost 10% of children or young adults who developed a cancer, regardless of their family history. This incidence may increase by the development of
Autor:
Léa Guerrini-Rousseau, Arnault Tauziède-Espariat, David Castel, Etienne Rouleau, Philipp Sievers, Raphaël Saffroy, Kévin Beccaria, Thomas Blauwblomme, Lauren Hasty, Franck Bourdeaut, Jacques Grill, Pascale Varlet, Marie-Anne Debily
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-4 (2023)
Externí odkaz:
https://doaj.org/article/fcb93cde8689407bb1f8654b19eec9d8
Autor:
Arnault Tauziède-Espariat, Aurore Siegfried, Yvan Nicaise, Thomas Kergrohen, Philipp Sievers, Alexandre Vasiljevic, Alexandre Roux, Edouard Dezamis, Chiara Benevello, Marie-Christine Machet, Sophie Michalak, Chloe 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, the RENOCLIP-LOC, the BIOMECA (Biomarkers for Ependymomas in Children, Adolescents) consortium
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-13 (2021)
Abstract The cIMPACT-NOW Update 7 has replaced the WHO nosology of “ependymoma, RELA fusion positive” by “Supratentorial-ependymoma, C11orf95-fusion positive”. This modification reinforces the idea that supratentorial-ependymomas exhibiting f
Externí odkaz:
https://doaj.org/article/760e1e11f97e4d039be01fc2b9183b94
Autor:
Callec L; Laetitia Callec, CHU- Hôpitaux de Brabois, Department of Pediatrics, Vandoeuvre les Nancy, France., Lardy-Cleaud A; Audrey Lardy-Cleaud, Department of Biostatistic, Centre Léon Bérard, Lyon, France., Guerrini-Rousseau L; Lea Guerrini-Rousseau, Department of Pediatric and Adolescents Oncology, Institut Gustave Roussy, Paris-Saclay University, Villejuif, France., Alapetite C; Claire Alapetite, Institut Curie, Department of Radiation Oncology, Paris, France., Vignon L; Lucie Vignon, INSERM, Paris-Descartes University, Department of Epidemiology, French National Registry of Childhood Solid Tumour Registry (RNTSE), Villejuif, France., Chastagner P; Pascal Chastagner, CHU- Hôpitaux de Brabois, Department of Pediatrics, Vandoeuvre les Nancy, France., Frappaz D; Didier Frappaz, Institut d'Hemato-oncologie Pediatrique, Lyon, France., Faure-Conter C; Cecile Faure-Conter, Institut d'Hemato-oncologie Pediatrique, Lyon, France. Electronic address: cecile.conter@ihope.fr.
Publikováno v:
European journal of cancer (Oxford, England : 1990) [Eur J Cancer] 2020 Sep; Vol. 136, pp. 186-194. Date of Electronic Publication: 2020 Jul 22.