Resultados de búsqueda - Marie‐Laure Moutard

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  1. 1
    Agitation and changes of Bispectral Index TM and electroencephalographic-derived variables during sevoflurane induction in children: clonidine premedication reduces agitation compared with midazolam †

    Agitation and changes of Bispectral Index TM and electroencephalographic-derived variables during sevoflurane induction in children: clonidine premedication reduces agitation compa... por Isabelle Constant, Y Leport, P Richard, Marie‐Laure Moutard, I. Murat

    Publicado 2004
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  2. 2
    Abnormal shape of the cavum septi pellucidi: an indirect sign of partial agenesis of the corpus callosum

    Abnormal shape of the cavum septi pellucidi: an indirect sign of partial agenesis of the corpus callosum por Ori Shen, A. Gélot, Marie‐Laure Moutard, Jean‐Marie Jouannic, Hen Y. Sela, Cathérine Garel

    Publicado 2015
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  3. 3
    Epileptogenic Effect of Sevoflurane

    Epileptogenic Effect of Sevoflurane por Stéphanie Gibert, Nada Sabourdin, Nicolas Louvet, Marie‐Laure Moutard, V Piat, Marie‐Laurence Guye, A. Rigouzzo, Isabelle Constant

    Publicado 2012
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  4. 4
    Identification of rare cortical folding patterns using unsupervised deep learning

    Identification of rare cortical folding patterns using unsupervised deep learning por Louise Guillon, Joël Chavas, A. Bénézit, Marie‐Laure Moutard, Pauline Roca, Charles Mellerio, Catherine Oppenheim, Denis Rivière, Jean‐François Mangin

    Publicado 2024
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  5. 5
    Prenatal abnormal features of the fourth ventricle in Joubert syndrome and related disorders

    Prenatal abnormal features of the fourth ventricle in Joubert syndrome and related disorders por E. Quarello, M. Molho, Cathérine Garel, A. Couture, M. P. Legac, Marie‐Laure Moutard, J. Bault, Catherine Fallet‐Bianco, Laurent Guibaud

    Publicado 2013
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  6. 6
    Organising white matter in a brain without corpus callosum fibres

    Organising white matter in a brain without corpus callosum fibres por A. Bénézit, Lucie Hertz‐Pannier, Ghislaine Dehaene‐Lambertz, Karla Monzalvo, David Germanaud, Delphine Duclap, Pamela Guevara, Jean‐François Mangin, Cyril Poupon, Marie‐Laure Moutard, Jessica Dubois

    Publicado 2014
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  7. 7
    STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients

    STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients por Cyril Mignot, Marie‐Laure Moutard, Oriane Trouillard, Isabelle Gourfinkel‐An, Aurélia Jacquette, Benoı̂t Arveiler, Fanny Morice‐Picard, Didier Lacombe, Catherine Chiron, Dorothée Ville, Perrine Charles, Eric Leguern, Christel Depienne, Delphine Héron

    Publicado 2011
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  8. 8
    Congenital cerebral malformations and dysfunction in fetuses and newborns following the 2013 to 2014 Zika virus epidemic in French Polynesia

    Congenital cerebral malformations and dysfunction in fetuses and newborns following the 2013 to 2014 Zika virus epidemic in French Polynesia por Marianne Besnard, Dominique Eyrolle‐Guignot, Prisca Guillemette-Artur, Stéphane Lastère, Frédérique Bost‐Bezeaud, Ludivine Marcelis, Véronique Abadie, Cathérine Garel, Marie‐Laure Moutard, Jean‐Marie Jouannic, Flore Rozenberg, Isabelle Leparc-Goffart, Henri‐Pierre Mallet

    Publicado 2016
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  9. 9
    Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis

    Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis por F. D’Antonio, G. Pagani, Alessandra Familiari, Asma Khalil, Tally-Lerman Sagies, G. Malinger, Z. Leibovitz, Cathérine Garel, Marie Laure Moutard, G. Pilu, Amar Bhidé, Ganesh Acharya, Martina Leombroni, Lamberto Manzoli, Aris T. Papageorghiou, Federico Prefumo

    Publicado 2016
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  10. 10
    Spectrum of epilepsy in terminal 1p36 deletion syndrome

    Spectrum of epilepsy in terminal 1p36 deletion syndrome por Nadia Bahi‐Buisson, Eva Guttierrez‐Delicado, Christine Soufflet, Marlène Rio, Valérie Cormier‐Daire, Didier Lacombe, Delphine Héron, Alain Verloès, Sameer M. Zuberi, Lydie Bürglen, Alexandra Afenjar, Marie Laure Moutard, Patrick Edery, Antonio Novelli, Laura Bernardini, Olivier Dulac, Rima Nabbout, Perrine Plouin, Agatino Battaglia

    Publicado 2007
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  11. 11
    GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex

    GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex por Nadia Bahi‐Buisson, Karine Poirier, Nathalie Boddaert, Catherine Fallet‐Bianco, Nicola Specchio, Enrico Bertini, Ahmet Okay Çağlayan, Karine Lascelles, Caroline Elie, Jérôme Rambaud, Michel Baulac, Isabelle An, Patrícia Dias, Vincent des Portes, Marie Laure Moutard, Christine Soufflet, Monique El Maleh, Chérif Beldjord, Laurent Villard, Jamel Chelly

    Publicado 2010
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  12. 12
    New human-specific brain landmark: The depth asymmetry of superior temporal sulcus

    New human-specific brain landmark: The depth asymmetry of superior temporal sulcus por F. Leroy, Qing Cai, Stéphanie L. Bogart, Jessica Dubois, Olivier Coulon, Karla Monzalvo, Clara Fischer, Hervé Glasel, Lise Van der Haegen, A. Bénézit, Ching‐Po Lin, David N. Kennedy, Aya Ihara, Lucie Hertz‐Pannier, Marie-Laure Moutard, Cyril Poupon, Marc Brysbaert, Neil Roberts, William D. Hopkins, Jean‐François Mangin, Ghislaine Dehaene‐Lambertz

    Publicado 2015
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  13. 13
    LIS1-Related Isolated Lissencephaly

    LIS1-Related Isolated Lissencephaly por Yoann Saillour, Nathalie Carion, Chloé Quēlin, Pierre‐Louis Léger, Nathalie Boddaert, Caroline Elie, Annick Toutain, Sandra Mercier, Marie Anne Barthez, Mathieu Milh, Sylvie Joriot, Vincent des Portes, Nicole Philip, D Broglin, Agathe Roubertie, G. Pitelet, Marie Laure Moutard, J.-M. Pinard, Clément Cancès, Claude Cancès, Anna Kaminśka, Jamel Chelly, Chérif Beldjord, Nadia Bahi‐Buisson

    Publicado 2009
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  14. 14
    Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities

    Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities por Martin W. Breuss, Julian Ik‐Tsen Heng, Karine Poirier, Guoling Tian, Xavier H. Jaglin, Zhengdong Qu, Andreas Braun, Thomas Gstrein, Linh Ngo, Matilda Haas, Nadia Bahi‐Buisson, Marie‐Laure Moutard, Sandrine Passemard, Alain Verloès, Pierre Gressèns, Yunli Xie, Kathryn Robson, Deepa Selvi Rani, Kumarasamy Thangaraj, Tim Clausen, Jamel Chelly, Nicholas J. Cowan, David A. Keays

    Publicado 2012
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  15. 15
    Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (<i>TUBA1A</i>)

    Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (<i>TUBA1A</i>) por Karine Poirier, David A. Keays, Fiona Francis, Yoann Saillour, Nadia Bahi, Sylvie Manouvrier, Catherine Fallet‐Bianco, Laurent Pasquier, Annick Toutain, Françoise Phan Dinh Tuy, Thierry Bienvenu, Sylvie Joriot, Sylvie Odent, Dorothée Ville, Isabelle Desguerre, Alice Goldenberg, Marie‐Laure Moutard, Jean‐Pierre Fryns, Hilde Van Esch, Victoria L. Harvey, Christian Siebold, Jonathan Flint, Chérif Beldjord, Jamel Chelly

    Publicado 2007
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  16. 16
    Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies

    Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic ence... por Stéphanie Valence, Emmanuelle Cochet, Christelle Rougeot, Cathérine Garel, Sandra Chantot‐Bastaraud, Élodie Lainey, Alexandra Afenjar, Marie-Anne Barthez, Nathalie Bednarek, Diane Doummar, Laurence Faivre, Cyril Goizet, Damien Haye, Bénédicte Héron, Isabelle Kemlin, Didier Lacombe, Mathieu Milh, Marie‐Laure Moutard, Florence Riant, Stéphanie Robin, Agathe Roubertie, Pierre Sarda, Annick Toutain, Laurent Villard, Dorothée Ville, Thierry Billette de Villemeur, Diana Rodriguez, Lydie Bürglen

    Publicado 2018
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  17. 17
    Reverse Phenotyping in Patients with Skin Capillary Malformations and Mosaic GNAQ or GNA11 Mutations Defines a Clinical Spectrum with Genotype-Phenotype Correlation

    Reverse Phenotyping in Patients with Skin Capillary Malformations and Mosaic GNAQ or GNA11 Mutations Defines a Clinical Spectrum with Genotype-Phenotype Correlation por Maud Jordan, Virginie Carmignac, Arthur Sorlin, Paul Kuentz, Juliette Albuisson, Luca Borradori, E. Bourrat, Odile Boute, Nenad Bukvić, A.‐C. Bursztejn, C. Chiavérini, Bruno Delobel, Marine Fournet, Jehanne Martel, Alice Goldenberg, S. Hadj‐Rabia, A. Mahé, A. Maruani, J. Mazereeuw‐Hautier, Cyril Mignot, Fanny Morice‐Picard, Marie‐Laure Moutard, Florence Petit, Justine Pasteur, Alice Phan, Sandra Whalen, Marjolaine Willems, Christophe Philippe, P. Vabres

    Publicado 2019
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  18. 18
    <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 por 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

    Publicado 2017
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  19. 19
    Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients

    Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients por Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, Erin L. Heinzen, Carmen Fons, Sanjay M. Sisodiya, Boukje de Vries, Christophe Goubau, Sarah Weckhuysen, David Kemlink, Ingrid E. Scheffer, Gaëtan Lesca, Muriel Rabilloud, Amna Klich, Alia Ramírez-Camacho, Adriana Ulate-Campos, Jaume Campistol, Melania Giannotta, Marie‐Laure Moutard, Diane Doummar, Cecile Hubsch-Bonneaud, Fatima Jaffer, J. Helen Cross, Fiorella Gurrieri, Francesco Danilo Tiziano, Soňa Nevšímalová, Sophie Nicole, Brian Neville, Arn M. J. M. van den Maagdenberg, Mohamad A. Mikati, David B. Goldstein, Rosaria Vavassori, Alexis Arzimanoglou

    Publicado 2015
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  20. 20
    Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation

    Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation por Solveig Heide, Myrtille Spentchian, Stéphanie Valence, Julien Buratti, Corinne Mach, Élodie Lejeune, Valérie Olin, Marta Massimello, Daphné Lehalle, L. Mouthon, Sandra Whalen, Anne Faudet, Cyril Mignot, Cathérine Garel, Éléonore Blondiaux, Mathilde Lefebvre, Geneviève Quenum-Miraillet, Sandra Chantot‐Bastaraud, Mathieu Milh, Florence Bretelle, Vincent des Portes, Laurent Guibaud, Audrey Putoux, V. Tsatsaris, Marta Spodenkiewic, Valérie Layet, Rodolphe Dard, Laurent Mandelbrot, Agnès Guët, Sébastien Moutton, Magali Gorce, Mathilde Nizon, Marie Vincent, Claire Bénéteau, Marie-Amélie Rocchisanni, Alexandra Benachi, Julien Saada, Tania Attié‐Bitach, Lucie Guilbaud, P Maurice, Stéphanie Friszer, Jean‐Marie Jouannic, Thierry Billette de Villemeur, Marie‐Laure Moutard, Boris Keren, Delphine Héron

    Publicado 2020
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