Risultati della ricerca - Aurélie Méneret

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  1. 1
    <i>ADCY5</i> mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias

    <i>ADCY5</i> mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias di Jennifer Friedman, Aurélie Méneret, Donghui Chen, Oriane Trouillard, Marie Vidailhet, Wendy H. Raskind, Emmanuel Roze

    Pubblicazione 2015
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  2. 2
    Cognitive and Psychiatric Adverse Effects of Foslevodopa/Foscarbidopa in Patients with Parkinson's Disease

    Cognitive and Psychiatric Adverse Effects of Foslevodopa/Foscarbidopa in Patients with Parkinson's Disease di Sacha Brohée, Emmanuel Roze, David Grabli, Hélène Letrillart, Lise Mantisi, Cendrine Foucard, Élodie Hainque, Florence Cormier, Aurélie Méneret, Fabien Hauw

    Pubblicazione 2025
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  3. 3
    Scoping Review on<scp>ADCY5</scp>‐Related Movement Disorders

    Scoping Review on<scp>ADCY5</scp>‐Related Movement Disorders di Poornima Jayadev Menon, Christelle Nilles, Laura Silveira‐Moriyama, Ruiyi Yuan, Claudio M. de Gusmão, Alexander Münchau, Miryam Carecchio, Steve Grossman, Gay Grossman, Aurélie Méneret, Emmanuel Roze, Tamara Pringsheim

    Pubblicazione 2023
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  4. 4
    Abnormalities of motor function, transcription and cerebellar structure in mouse models of<i>THAP1</i>dystonia

    Abnormalities of motor function, transcription and cerebellar structure in mouse models of<i>THAP1</i>dystonia di Marta Ruiz, Georgina Pérez-García, Maitane Ortiz‐Virumbrales, Aurélie Méneret, Andrika Morant, Jessica Kottwitz, Tania Fuchs, Justine Bonet, Pedro Gonzalez‐Alegre, Patrick R. Hof, Laurie J. Ozelius, Michelle E. Ehrlich

    Pubblicazione 2015
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  5. 5
    RAD51 deficiency disrupts the corticospinal lateralization of motor control

    RAD51 deficiency disrupts the corticospinal lateralization of motor control di Cécile Gallea, Traian Popa, Cécile Hubsch, Romain Valabrègue, Vanessa Brochard, Prantik Kundu, Benoît Schmitt, Éric Bardinet, Eric Bertasi, Constance Flamand‐Roze, Nicolas Alexandre, Christine Delmaire, Aurélie Méneret, Christel Depienne, Cyril Poupon, Lucie Hertz‐Pannier, M. Cincotta, Marie Vidailhet, Stéphane Lehericy, Sabine Meunier, Emmanuel Roze

    Pubblicazione 2013
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  6. 6
    The supplementary motor area modulates interhemispheric interactions during movement preparation

    The supplementary motor area modulates interhemispheric interactions during movement preparation di Quentin Welniarz, Cécile Gallea, Jean‐Charles Lamy, Aurélie Méneret, Traian Popa, Romain Valabrègue, Benoît Béranger, Vanessa Brochard, Constance Flamand‐Roze, Oriane Trouillard, Cécilia Bonnet, Norbert Brüggemann, Pierre Bitoun, Bertrand Degos, Cécile Hubsch, Élodie Hainque, Jean‐Louis Golmard, Marie Vidailhet, Stéphane Lehéricy, Isabelle Dusart, Sabine Meunier, Emmanuel Roze

    Pubblicazione 2019
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  7. 7
    Increased diagnostic yield in complex dystonia through exome sequencing

    Increased diagnostic yield in complex dystonia through exome sequencing di Thomas Wirth, Christine Tranchant, Nathalie Drouot, Boris Keren, Cyril Mignot, Laura Cif, Romain Lefaucheur, Laurence Lion‐François, Aurélie Méneret, Domitille Gras, Emmanuel Roze, Cécile Laroche, Pierre Burbaud, Stéphanie Bannier, Ouhaïd Lagha‐Boukbiza, Marie‐Aude Spitz, Vincent Laugel, Matthieu Béreau, Emmanuelle Ollivier, Patrick Nitschké, Diane Doummar, Gabrielle Rudolf, Mathieu Anheim, Jamel Chelly

    Pubblicazione 2020
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  8. 8
    Long-term effect of apomorphine infusion in advanced Parkinson’s disease: a real-life study

    Long-term effect of apomorphine infusion in advanced Parkinson’s disease: a real-life study di Bruna Meira, Bertrand Degos, Elise Corsetti, Mohamed Doulazmi, Emeline Berthelot, Clara Virbel-Fleischman, Pauline Dodet, Aurélie Méneret, Louise‐Laure Mariani, Cécile Delorme, Florence Cormier‐Dequaire, David Bendetowicz, Nicolas Villain, Clément Tarrano, Lise Mantisi, Hélène Letrillart, Céline Louapre, Eavan McGovern, Yulia Worbe, David Grabli, Marie Vidailhet, Élodie Hainque, Emmanuel Roze

    Pubblicazione 2021
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  9. 9
    RAD51 Haploinsufficiency Causes Congenital Mirror Movements in Humans

    RAD51 Haploinsufficiency Causes Congenital Mirror Movements in Humans di Christel Depienne, Delphine Bouteiller, Aurélie Méneret, S. Billot, Sergiu Groppa, Stephan Klebe, Fanny Charbonnier‐Beaupel, Jean‐Christophe Corvol, Jean‐Paul Saraiva, Norbert Brueggemann, Kailash P. Bhatia, M. Cincotta, Vanessa Brochard, Constance Flamand‐Roze, Wassila Carpentier, Sabine Meunier, Yannick Marie, Marion Gaussen, Giovanni Stévanin, Rosine Wehrlé, Marie Vidailhet, Christine Klein, Isabelle Dusart, Alexis Brice, Emmanuel Roze

    Pubblicazione 2012
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  10. 10
    Mutations in the netrin-1 gene cause congenital mirror movements

    Mutations in the netrin-1 gene cause congenital mirror movements di Aurélie Méneret, Elizabeth A. Franz, Oriane Trouillard, Thomas Oliver, Yvrick Zagar, Stephen P. Robertson, Quentin Welniarz, R. J. M. Gardner, Cécile Gallea, Myriam Srour, Christel Depienne, Christine L. Jasoni, Caroline Dubacq, Florence Riant, Jean‐Charles Lamy, Marie‐Pierre Morel, Raphaël Guérois, Jessica Andréani, Coralie Fouquet, Mohamed Doulazmi, Marie Vidailhet, Guy A. Rouleau, Alexis Brice, Alain Chédotal, Isabelle Dusart, Emmanuel Roze, David Markie

    Pubblicazione 2017
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  11. 11
    Congenital mirror movements

    Congenital mirror movements di Aurélie Méneret, Christel Depienne, Florence Riant, Oriane Trouillard, Delphine Bouteiller, M. Cincotta, Pierre Bitoun, Julia Wickert, Lagroua Isabelle, Ana Westenberger, Alessandra Borgheresi, Diane Doummar, Marcello Romano, Símone Rossi, Luc Defebvre, Linda De Meırleır, Alberto J. Espay, Simona Fiori, Stephan Klebe, Chloé Quēlin, Sabine Rudnik–Schöneborn, Ghislaine Plessis, Russell C. Dale, Susan Sklower Brooks, Karolina Dzieżyc, Pierre Pollak, Jean‐Louis Golmard, Marie Vidailhet, Alexis Brice, Emmanuel Roze

    Pubblicazione 2014
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  12. 12
    <i>DCC</i>mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome

    <i>DCC</i>mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome di Ashley P.L. Marsh, Timothy J. Edwards, Charles A. Galea, Helen Cooper, Elizabeth C. Engle, Saumya Shekhar Jamuar, Aurélie Méneret, Marie‐Laure Moutard, Caroline Nava, Agnès Rastetter, Gail Robinson, Guy A. Rouleau, Emmanuel Roze, Megan Spencer‐Smith, Oriane Trouillard, Thierry Billette de Villemeur, Christopher A. Walsh, Timothy W. Yu, Delphine Héron, Elliott H. Sherr, Linda J. Richards, Christel Depienne, Richard J. Leventer, Paul J. Lockhart

    Pubblicazione 2017
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  13. 13
    <i>ADCY5</i> -related dyskinesia

    <i>ADCY5</i> -related dyskinesia di Donghui Chen, Aurélie Méneret, Jennifer Friedman, Olena Korvatska, Alona Gad, Emily Bonkowski, Holly A.F. Stessman, Diane Doummar, Cyril Mignot, Mathieu Anheim, Saunder Bernes, Marie Y. Davis, Nathalie Damon‐Perrière, Bertrand Degos, David Grabli, Domitille Gras, Fuki M. Hisama, Katherine M. Mackenzie, Phillip D. Swanson, Christine Tranchant, Marie Vidailhet, Steven P. Winesett, Oriane Trouillard, Laura M. Amendola, Michael O. Dorschner, Michael D. Weiss, Evan E. Eichler, Ali Torkamani, Emmanuel Roze, Thomas D. Bird, Wendy H. Raskind

    Pubblicazione 2015
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  14. 14
    Highlighting the Dystonic Phenotype Related to <scp><i>GNAO1</i></scp>

    Highlighting the Dystonic Phenotype Related to <scp><i>GNAO1</i></scp> di Thomas Wirth, Giacomo Garone, Manju A. Kurian, Amélie Piton, Francisca Millan, Aida Telegrafi, Nathalie Drouot, Gabrielle Rudolf, Jamel Chelly, Warren A. Marks, Lydie Bürglen, Diane Demailly, Phillipe Coubes, Mayté Castro Jimenez, Sylvie Joriot, Jamal Ghoumid, Jérémie Belin, Jean‐Marc Faucheux, Lubov Blumkin, Mariam Hull, Mered Parnes, Claudia Ravelli, Gaëtan Poulen, Nadège Calmels, Andrea H. Németh, Martin A. Smith, Angela Barnicoat, Claire Ewenczyk, Aurélie Méneret, Emmanuel Roze, Boris Keren, Cyril Mignot, Christophe Béroud, Fernando Delgado Acosta, C. Nowak, William G. Wilson, Dora Steel, Alessandro Capuano, Marie Vidailhet, Jean‐Pierre Lin, Christine Tranchant, Laura Cif, Diane Doummar, Mathieu Anheim

    Pubblicazione 2022
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  15. 15
    Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype

    Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype di Lou Grangeon, David Wallon, Camille Charbonnier, Olivier Quenez, Anne‐Claire Richard, Stéphane Rousseau, Clara Budowski, Thibaud Lebouvier, Anne-Gaëlle Corbillé, Marie Vidailhet, Aurélie Méneret, Emmanuel Roze, Mathieu Anheim, Christine Tranchant, Pascal Favrole, Jean‐Christophe Antoine, Luc Defebvre, Xavier Ayrignac, Pierre Labauge, Jérémie Pariente, Michel Clanet, David Maltête, Anne Rovelet‐Lecrux, Anne Boland, Jean‐François Deleuze, Pascal Favrole, Christophe Verny, Pierre Krystkowiak, Ludivine Chamard, Sébastien Moutton, Cyril Goizet, Claude Férec, Serge Timsit, S. Schaeffer, Nathalie Derache, Gilles Defer, Franck Durif, François Sellal, Olivier Rouaud, Christel Thauvin‐Robinet, Stéphanie Cubizolle, Mathilde Sauvée, Amélie Leblanc, Alexis Demas, Alice Poisson, Elisabeth Tournier‐Lasserve, Dominique Hervé, Hugues Chabriat, Guillaume Grolez, Nicolas Carrière, Luc Defebvre, Thibaud Lebouvier, Tatiana Witjas, Jean‐Philippe Azulay, Frédérique Fluchère, Mira Didic, Karine Nguyen, Mahmoud Charif, Xavier Ayrignac, Pierre Labauge, C. Lionnet, Cécilia Marelli, Simon Gaud, Tiphaine Rouaud, Brice Laurens, Emmanuelle Folgoas, Bertrand Isidor, Jean Chiésa, Maud Pallix-Guyot, Nicolas Gaillard, Nadège Olivier, Snejana Jurici, Isabelle Marey, Perrine Charles, Claire Ewenczyck, Alexandra Dürr, Cécile Hubsch, Aurélie Méneret, Marie Vidailhet, Yann Nadjar, Isabelle Le Ber, David Grabli, Emmanuel Roze, Vincent Navarro, Sylvie Mecharles-Darrigol, Julien Lagarde, Marie Sarazin, Marc Vérin, Romain Lefaucheur, David Maltête, David Wallon, Didier Hannequin, Olivier Martinaud, Lucie Guyant‐Maréchal, Gaël Nicolas, Thierry Frébourg, Anne‐Claire Richard, Dominique Campion, Olivier Guillin, Marion Yger

    Pubblicazione 2019
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  16. 16
    Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions

    Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions di Jean‐Loup Méreaux, Claire-Sophie Davoine, David Pellerin, Giulia Coarelli, Marie Coutelier, Claire Ewenczyk, Marie‐Lorraine Monin, Mathieu Anheim, Isabelle Le Ber, Stéphane Thobois, Florent Gobert, Léna Guillot‐Noël, Sylvie Forlani, Ludmila Jornéa, Anna Heinzmann, Aude Sangaré, Bertrand Gaymard, Lucie Guyant‐Maréchal, Perrine Charles, Cécilia Marelli, Jérôme Honnorat, Bertrand Degos, François Tison, Sophie Sangla, M. Simonetta‐Moreau, François Salachas, Maya Tchikviladzé, Giovanni Castelnovo, Fanny Mochel, Stephan Klebe, Anna Castrioto, Silvia Fenu, Aurélie Méneret, Frédéric Bourdain, Marion Wandzel, Virginie Roth, Céline Bonnet, Florence Riant, Giovanni Stévanin, Sandrine Noël, Anne‐Laure Fauret‐Amsellem, Melanie Bahlo, Paul J. Lockhart, Bernard Brais, Mathilde Renaud, Alexis Brice, Alexandra Dürr

    Pubblicazione 2023
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  17. 17
    Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

    Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance di Ashley P.L. Marsh, Delphine Héron, Timothy J. Edwards, Angélique Quartier, Charles A. Galea, Caroline Nava, Agnès Rastetter, Marie-Laure Moutard, Vicki Anderson, Pierre Bitoun, Jens Bunt, Anne Faudet, Cathérine Garel, Greta Gillies, Ilan Gobius, Justine Guégan, Solveig Heide, Boris Keren, Fabien Lesne, Vesna Lukić, Simone Mandelstam, George McGillivray, Alissandra McIlroy, Aurélie Méneret, Cyril Mignot, Laura Morcom, Sylvie Odent, Annalisa Paolino, Kate Pope, Florence Riant, Gail Robinson, Megan Spencer‐Smith, Myriam Srour, Sarah Stephenson, Rick M. Tankard, Oriane Trouillard, Quentin Welniarz, Amanda Wood, Alexis Brice, Guy A. Rouleau, Tania Attié‐Bitach, Martin B. Delatycki, Jean‐Louis Mandel, David J. Amor, Emmanuel Roze, Amélie Piton, Melanie Bahlo, Thierry Billette de Villemeur, Elliott H. Sherr, Richard J. Leventer, Linda J. Richards, Paul J. Lockhart, Christel Depienne

    Pubblicazione 2017
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  18. 18
    Severe COVID-19-related encephalitis can respond to immunotherapy

    Severe COVID-19-related encephalitis can respond to immunotherapy di Albert Cao, Benjamin Rohaut, Loïc Le Guennec, Samir Saheb, Clémence Marois, Victor Altmayer, Vincent T. Carpentier, Safaa Nemlaghi, Marie Soulié, Quentin Morlon, Bryan Berthet-Delteil, Alexandre Bleibtreu, Mathieu Raux, Nicolas Weiss, Sophie Demeret, Cécile Delorme, Jean‐Christophe Corvol, Jean‐Yves Delattre, Stéphanie Carvalho, Sandrine Sagnes, Bruno Dubois, Vincent Navarro, Céline Louapre, Tanya Stojkovic, Ahmed Idbaih, Charlotte Rosso, David Grabli, Ana Gales, Bruno Millet, Benjamin Rohaut, É. Bayen, Sophie Dupont, Gaëlle Bruneteau, Stéphane Lehéricy, Danielle Seilhean, Alexandra Dürr, Aurélie Kas, Foudil Lamari, Marion Houot, Vanessa Batista Brochard, Sophie Dupont, Catherine Lubetzki, Danielle Seilhean, P. Pradat-Diehl, Charlotte Rosso, Khê Hoang‐Xuan, Bertrand Fontaine, Lionel Naccache, Philippe Fossati, Isabelle Arnulf, Alexandra Dürr, Alexandre Carpentier, Stéphane Lehéricy, Yves Edel, Anna Luisa Di Stefano, G. Robain, Philippe Thoumie, Bertrand Degos, Tarek Sharshar, Sonia Alamowitch, Emmanuelle Apartis-Bourdieu, Charles-Siegried Peretti, Rénata Ursu, Nathalie Dzierzynski, Kiyoka Kinugawa Bourron, Joel Belmin, Bruno Oquendo, Éric Pautas, Marc Verny, Cécile Delorme, Jean‐Christophe Corvol, Jean‐Yves Delattre, Yves Samson, Sara Leder, Anne Leger, Sandrine Deltour, Flore Baronnet, Ana Gales, Stéphanie Bombois, Mehdi Touat, Ahmed Idbaih, Marc Sanson, Caroline Dehais, Caroline Houillier, Florence Laigle-Donadey, Dimitri Psimaras, Agusti Alenton, Nadia Younan, Nicolas Villain, David Grabli, Maria del Mar Amador, Gaëlle Bruneteau, Céline Louapre, Louise‐Laure Mariani, Nicolas Mezouar, Graziella Mangone, Aurelie Meneret, Andreas Hartmann, Clément Tarrano, David Bendetowicz

    Pubblicazione 2020
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  19. 19
    The cerebral network of COVID-19-related encephalopathy: a longitudinal voxel-based 18F-FDG-PET study

    The cerebral network of COVID-19-related encephalopathy: a longitudinal voxel-based 18F-FDG-PET study di Aurélie Kas, M. Soret, Nadya Pyatigoskaya, Marie‐Odile Habert, Adèle Hesters, Loïc Le Guennec, Olivier Paccoud, Stéphanie Bombois, Cécile Delorme, Cécile Delorme, Jean‐Christophe Corvol, Jean‐Yves Delattre, Stéphanie Carvalho, Sandrine Sagnes, Bruno Dubois, Vincent Navarro, Céline Louapre, Tanya Stojkovic, Ahmed Idbaih, Charlotte Rosso, David Grabli, Ana Gales, Bruno Millet, Benjamin Rohaut, É. Bayen, Sophie Dupont, Gaëlle Bruneteau, Stéphane Lehéricy, Danielle Seilhean, Alexandra Dürr, Aurélie Kas, Foudil Lamari, Marion Houot, Vanessa Batista Brochard, Sophie Dupont, Catherine Lubetzki, Danielle Seilhean, P. Pradat-Diehl, Charlotte Rosso, Khê Hoang‐Xuan, Bertrand Fontaine, Lionel Naccache, Philippe Fossati, Isabelle Arnulf, Alexandra Dürr, Alexandre Carpentier, Stéphane Lehéricy, Yves Edel, Anna Luisa Di Stefano, G. Robain, P. Thoumie, Bertrand Degos, Tarek Sharshar, Sonia Alamowitch, Emmanuelle Apartis-Bourdieu, Charles-Siegried Peretti, Rénata Ursu, Nathalie Dzierzynski, Kiyoka Kinugawa Bourron, Joël Belmin, Bruno Oquendo, Éric Pautas, Marc Verny, Cécile Delorme, Jean‐Christophe Corvol, Jean‐Yves Delattre, Yves Samson, Sara Leder, Anne Léger, Sandrine Deltour, Flore Baronnet, Ana Gales, Stéphanie Bombois, Mehdi Touat, Ahmed Idbaih, Marc Sanson, Caroline Dehais, Caroline Houillier, Florence Laigle–Donadey, Dimitri Psimaras, Agusti Alenton, Nadia Younan, Nicolas Villain, David Grabli, Maria del Mar Amador, Gaëlle Bruneteau, Céline Louapre, Louise‐Laure Mariani, Nicolas Mezouar, Graziella Mangone, Aurélie Méneret, Andreas Hartmann, Clément Tarrano, David Bendetowicz, Pierre‐François Pradat, Michel Baulac, Sara Sambin, François Salachas, Nadine Le Forestier, Phintip Pichit

    Pubblicazione 2021
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  20. 20
    Association of Clinical, Biological, and Brain Magnetic Resonance Imaging Findings With Electroencephalographic Findings for Patients With COVID-19

    Association of Clinical, Biological, and Brain Magnetic Resonance Imaging Findings With Electroencephalographic Findings for Patients With COVID-19 di Virginie Lambrecq, Aurélie Hanin, Esteban Munoz‐Musat, Lydia Chougar, Salimata Gassama, Cécile Delorme, Louis Cousyn, Alaina Borden, Maria Damiano, Valério Frazzini, Gilles Huberfeld, Frank Landgraf, Vi‐Huong Nguyen‐Michel, Phintip Pichit, Aude Sangaré, Mario Chávez, Capucine Morélot-Panzini, Élise Morawiec, Mathieu Raux, Charles‐Édouard Luyt, Pierre Rufat, Damien Galanaud, Jean‐Christophe Corvol, Catherine Lubetzki, Benjamin Rohaut, Sophie Demeret, Nadya Pyatigorskaya, Lionel Naccache, Vincent Navarro, Jean‐Yves Delattre, Stéphanie Carvalho, Sandrine Sagnes, Bruno Dubois, Céline Louapre, Tanya Stojkovic, Ahmed Idbaih, Charlotte Rosso, David Grabli, Ana Gales, Bruno Millet, É. Bayen, Sophie Dupont, Gaëlle Bruneteau, Stéphane Lehéricy, Danielle Seilhean, Alexandra Dürr, Aurélie Kas, Foudil Lamari, Marion Houot, Vanessa Batista Brochard, P. Pradat-Diehl, Khê Hoang‐Xuan, Bertrand Fontaine, Philippe Fossati, Isabelle Arnulf, Alexandre Carpentier, Yved Edel, Di Stefano Anna Luisa, G. Robain, P. Thoumie, Bertrand Degos, Tarek Sharshar, Sonia Alamowitch, Emmanuelle Apartis-Bourdieu, Charles-Siegried Peretti, Rénata Ursu, Nathalie Dzierzynski, Kiyoka Kinugawa Bourron, Joel Belmin, Bruno Oquendo, Éric Pautas, Marc Verny, Yves Samson, Sara Leder, Anne Léger, Sandrine Deltour, Flore Baronnet, Stéphanie Bombois, Mehdi Touat, Caroline Dehais, Caroline Houillier, Florence Laigle-Donadey, Dimitri Psimaras, Agustí Alentorn, Nadia Younan, Nicolas Villain, Maria del Mar Amador, Louise‐Laure Mariani, Nicolas Mezouar, Graziella Mangone, Aurélie Méneret, Andreas Hartmann, Clément Tarrano, David Bendetowicz, Pierre‐François Pradat, Michel Baulac, Sara Sambin, F Chochon, Adèle Hesters, Bastien Herlin

    Pubblicazione 2021
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