Both L-DOPA and HFS-STN restore the enhanced group II spinal reflex excitation to a normal level in patients with Parkinson’s disease von Marchand-Pauvert, V, Gerdelat-Mas, A, Ory-Magne, F, Calvas, F, Mazevet, D, Meunier, S, Brefel-Courbon, C, Vidailhet, M, Simonetta-Moreau, M

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O42 L’administration d’apeline améliore la sensibilité à l’insuline: preuve de concept chez le volontaire sain en surpoids von Gourdy, P, Cazals, L, Thalamas, C, Lami, E, Sommet, A, Galitzky, M, Calvas, F, Castan-Laurell, I, Valet, P

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Apomorphine effect on pain threshold in Parkinson's disease: A clinical and positron emission tomography study von Dellapina, Estelle, Gerdelat-Mas, Angélique, Ory-Magne, Fabienne, Pourcel, Laure, Galitzky, Monique, Calvas, Fabienne, Simonetta-Moreau, Marion, Thalamas, Claire, Payoux, Pierre, Brefel-Courbon, Christine

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L’administration d’apeline améliore la sensibilité à l’insuline : preuve de concept chez le volontaire sain en surpoids von Gourdy, P., Pr, Cazals, L, Thalamas, C., Dr, Emmanuelle, L, Sommet, A., Dr, Calvas, F., Dr, Galitzky, M., Dr, Castan-Laurell, I., Pr, Valet, P., Pr

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Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY von Orth, Michael

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How to Capitalize on the Retest Effect in Future Trials on Huntington's Disease von Schramm, Catherine, Katsahian, Sandrine, Youssov, Katia, Démonet, Jean-François, Krystkowiak, Pierre, Supiot, Frédéric, Verny, Christophe, Cleret de Langavant, Laurent, Bachoud-Lévi, Anne-Catherine

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G01 Neural correlates of empathy and context evaluation in Huntington's disease patients von Lepron, E, Gros, H, Calvas, F, Viallard, G, Démonet, J-F

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Validation of a risk-assessment scale and a risk-adapted monitoring plan for academic clinical research studies — The Pre-Optimon study von Journot, Valérie, Pignon, Jean-Pierre, Gaultier, Claude, Daurat, Véronique, Bouxin-Métro, Annie, Giraudeau, Bruno, Preux, Pierre-Marie, Tréluyer, Jean-Marc, Chevret, Sylvie, Plättner, Valérie, Thalamas, Claire, Clisant, Stéphanie, Ravaud, Philippe, Chêne, Geneviève

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Traitement de la maladie d’Alzheimer : une lueur au bout du tunnel ? von Pariente, J., Rafiq, M., Benaiteau, M., Gouilly, D., Pomies, E., Jasse, L., Drif, A., Calvas, F., Payoux, P., Rascol, O., Thalamas, C.

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Inequality and Growth von Basu, Kaushik, Stiglitz, Joseph E

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Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach von Liautard-Haag, C., Durif, G., VanGoethem, C., Baux, D., Louis, A., Cayrefourcq, L., Lamairia, M., Willems, M., Zordan, C., Dorian, V., Rooryck, C., Goizet, C., Chaussenot, A., Monteil, L., Calvas, P., Miry, C., Favre, R., Le Boette, E., Fradin, M., Roux, A. F., Cossée, M., Koenig, M., Alix-Panabière, C., Guissart, C., Vincent, M. C.

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Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia von Plaisancié, J., Ceroni, F., Holt, R., Zazo Seco, C., Calvas, P., Chassaing, N., Ragge, Nicola K.

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Implication of non-coding PAX6 mutations in aniridia von Plaisancié, Julie, Tarilonte, M., Ramos, P., Jeanton-Scaramouche, C., Gaston, V., Dollfus, H., Aguilera, D., Kaplan, J., Fares-Taie, L., Blanco-Kelly, F., Villaverde, C., Francannet, C., Goldenberg, A., Arroyo, I., Rozet, J. M., Ayuso, C., Chassaing, N., Calvas, P., Corton, M.

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Compositional diversity of rehabilitated tropical lands supports multiple ecosystem services and buffers uncertainties von Knoke, Thomas, Paul, Carola, Hildebrandt, Patrick, Calvas, Baltazar, Castro, Luz Maria, Härtl, Fabian, Döllerer, Martin, Hamer, Ute, Windhorst, David, Wiersma, Yolanda F., Curatola Fernández, Giulia F., Obermeier, Wolfgang A., Adams, Julia, Breuer, Lutz, Mosandl, Reinhard, Beck, Erwin, Weber, Michael, Stimm, Bernd, Haber, Wolfgang, Fürst, Christine, Bendix, Jörg

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International incidence of childhood cancer, 2001–10: a population-based registry study von Steliarova-Foucher, Eva, Dr, Colombet, Murielle, MSc, Ries, Lynn A G, MS, Moreno, Florencia, PhD, Dolya, Anastasia, MSc, Bray, Freddie, PhD, Hesseling, Peter, PhD, Shin, Hee Young, PhD, Stiller, Charles A, MSc

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Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants von Lerat, J., Magdelaine, C., Lunati, A., Dzugan, H., Dejoie, C., Rego, M., Beze Beyrie, P., Bieth, E., Calvas, P., Cintas, P., Delaubrier, A., Demurger, F., Gilbert-Dussardier, B., Goizet, C., Journel, H., Laffargue, F., Magy, L., Taithe, F., Toutain, A., Urtizberea, J.A., Sturtz, F., Lia, A.S.

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Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta von Caron, Véronique, Chassaing, Nicolas, Ragge, Nicola, Boschann, Felix, Ngu, Angelina My-Hoa, Meloche, Elisabeth, Chorfi, Sarah, Lakhani, Saquib A., Ji, Weizhen, Steiner, Laurie, Marcadier, Julien, Jansen, Philip R., van de Pol, Laura A., van Hagen, Johanna M., Russi, Alvaro Serrano, Le Guyader, Gwenaël, Nordenskjöld, Magnus, Nordgren, Ann, Anderlid, Britt-Marie, Plaisancié, Julie, Stoltenburg, Corinna, Horn, Denise, Drenckhahn, Anne, Hamdan, Fadi F., Lefebvre, Mathilde, Attie-Bitach, Tania, Forey, Peggy, Smirnov, Vasily, Ernould, Françoise, Jacquemont, Marie-Line, Grotto, Sarah, Alcantud, Alberto, Coret, Alicia, Ferrer-Avargues, Rosario, Srivastava, Siddharth, Vincent-Delorme, Catherine, Romoser, Shelby, Safina, Nicole, Saade, Dimah, Lupski, James R., Calame, Daniel G., Geneviève, David, Chatron, Nicolas, Schluth-Bolard, Caroline, Myers, Kenneth A., Dobyns, William B., Calvas, Patrick, Salmon, Caroline, Holt, Richard, Elmslie, Frances, Allaire, Marc, Prigozhin, Daniil M., Tremblay, André, Michaud, Jacques L.

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Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype–phenotype correlations as a strategy for molecula... von Hanein, Sylvain, Perrault, Isabelle, Gerber, Sylvie, Tanguy, Gaëlle, Barbet, Fabienne, Ducroq, Dominique, Calvas, Patrick, Dollfus, Hélène, Hamel, Christian, Lopponen, Tuija, Munier, Francis, Santos, Louisa, Shalev, Stavit, Zafeiriou, Dimitrios, Dufier, Jean‐Louis, Munnich, Arnold, Rozet, Jean‐Michel, Kaplan, Josseline

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X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family von Laumonnier, Frédéric, Bonnet-Brilhault, Frédérique, Gomot, Marie, Blanc, Romuald, David, Albert, Moizard, Marie-Pierre, Raynaud, Martine, Ronce, Nathalie, Lemonnier, Eric, Calvas, Patrick, Laudier, Béatrice, Chelly, Jamel, Fryns, Jean-Pierre, Ropers, Hans-Hilger, Hamel, Ben C.J., Andres, Christian, Barthélémy, Catherine, Moraine, Claude, Briault, Sylvain

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Incidence of childhood cancer in Latin America and the Caribbean: coverage, patterns, and time trends von de Paula Silva, Neimar, Colombet, Murielle, Moreno, Florencia, Erdmann, Friederike, Dolya, Anastasia, Piñeros, Marion, Stiller, Charles A, Steliarova-Foucher, Eva

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