Pressure effects on kinetics and decay processes in xenon after selective photoexcitation von MOUTARD, P, LAPORTE, P, SUBTIL, J.-L, DAMANY, N, DAMANY, H

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Pressure effect on 6p-6s ir decay in xenon after two-photon excitation von Moutard, P., Laporte, P., Damany, N., Subtil, J.L., Damany, H.

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Pressure effects on kinetics and decay processes in argon under selective photoexcitation von MOUTARD, P, LAPORTE, P, SUBTIL, J.-L, DAMANY, N, DAMANY, H

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Optical-optical double resonance involving the coupling of a vacuum-ultraviolet spark source with a laser: two-step excitation in rare gases von MOUTARD, P, LAPORTE, P, BON, M, DAMANY, N, DAMANY, H

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Spectroscopy and photochemistry of Au aggregates in rare gas matrices von Markus, Rudolf, Moutard, Pascal, Chergui, Majed, Schwentner, Nikolaus

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Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesions von Maurice, P., Guilbaud, L., Garel, J., Mine, M., Dugas, A., Friszer, S., Maisonneuve, E., Moutard, M.‐L., Coste, T., Héron, D., Tournier‐Lasserve, E., Garel, C., Jouannic, J.‐M.

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Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients von Chérot, E., Keren, B., Dubourg, C., Carré, W., Fradin, M., Lavillaureix, A., Afenjar, A., Burglen, L., Whalen, S., Charles, P., Marey, I., Heide, S., Jacquette, A., Heron, D., Doummar, D., Rodriguez, D., Billette de Villemeur, T., Moutard, M.‐L., Guët, A., Xavier, J., Périsse, D., Cohen, D., Demurger, F., Quélin, C., Depienne, C., Odent, S., Nava, C., David, V., Pasquier, L., Mignot, C.

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Feasibility and Added Value of Fetal DTI Tractography in the Evaluation of an Isolated Short Corpus Callosum: Preliminary Results von Millischer, A-E, Grevent, D, Sonigo, P, Bahi-Buisson, N, Desguerre, I, Mahallati, H, Bault, J-P, Quibel, T, Couderc, S, Moutard, M-L, Julien, E, Dangouloff, V, Bessieres, B, Malan, V, Attie, T, Salomon, L-J, Boddaert, N

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Normal EEG in childhood: From neonates to adolescents von Eisermann, M, Kaminska, A, Moutard, M.-L, Soufflet, C, Plouin, P

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

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Five new TTF1/NKX2.1 mutations in brain–lung–thyroid syndrome: rescue by PAX8 synergism in one case von Carré, Aurore, Szinnai, Gabor, Castanet, Mireille, Sura-Trueba, Sylvia, Tron, Elodie, Broutin-L’Hermite, Isabelle, Barat, Pascal, Goizet, Cyril, Lacombe, Didier, Moutard, Marie-Laure, Raybaud, Christine, Raynaud-Ravni, Catherine, Romana, Serge, Ythier, Hubert, Léger, Juliane, Polak, Michel

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Investigating the Ultracompact X-Ray Binary Candidate SLX 1735-269 with NICER and NuSTAR von Moutard, D. L., Ludlam, R. M., Sudha, M., Buisson, D. J. K., Cackett, E. M., Degenaar, N., Fabian, A. C., Gandhi, P., García, J. A., Shaw, A. W., Tomsick, J. A.

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The VIPERS Multi-Lambda Survey: II. Diving with massive galaxies in 22 square degrees since z = 1.5 von Moutard, T, Arnouts, S, Ilbert, O, Coupon, J, Davidzon, I, Guzzo, L, Hudelot, P, McCracken, H J, Werbaeke, L Van, Morrison, G E

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The VIPERS Multi-Lambda Survey: I. UV and near-IR observations, multi-colour catalogues, and photometric redshifts von Moutard, T, Arnouts, S, Ilbert, O, Coupon, J, Hudelot, P, Vibert, D, Comte, V, Conseil, S, Davidzon, I, Guzzo, L

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Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosis von Massoud, M., Cagneaux, M., Garel, C., Varene, N., Moutard, M.‐L., Billette, T., Benezit, A., Rougeot, C., Jouannic, J.‐M., Massardier, J., Gaucherand, P., Desportes, V., Guibaud, L.

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Environments of red nuggets at z ∼ 0.7 from the VIPERS survey von Siudek, M, Lisiecki, K, Krywult, J, Donevski, D, Haines, C P, Karska, A, Małek, K, Moutard, T, Pollo, A

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

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The VIMOS Public Extragalactic Redshift Survey (VIPERS): galaxy segregation inside filaments at z ≃ 0.7 von Malavasi, N, Arnouts, S, Vibert, D, de la Torre, S, Moutard, T, Pichon, C, Davidzon, I, Kraljic, K, Bolzonella, M, Guzzo, L, Garilli, B, Scodeggio, M, Granett, B R, Abbas, U, Adami, C, Bottini, D, Cappi, A, Cucciati, O, Franzetti, P, Fritz, A, Iovino, A, Krywult, J, Le Brun, V, Le Fevre, O, Maccagni, D, Malek, K, Marulli, F, Polletta, M, Pollo, A, Tasca, L, Tojeiro, R, Vergani, D, Zanichelli, A, Bel, J, Branchini, E, Coupon, J, De Lucia, G, Dubois, Y, Hawken, A, Ilbert, O, Laigle, C, Moscardini, L, Sousbie, T, Treyer, M, Zamorani, G

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Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling? von El Chehadeh, S., Touraine, R., Prieur, F., Reardon, W., Bienvenu, T., Chantot‐Bastaraud, S., Doco‐Fenzy, M., Landais, E., Philippe, C., Marle, N., Callier, P., Mosca‐Boidron, A.‐L., Mugneret, F., Le Meur, N., Goldenberg, A., Guerrot, A.‐M., Chambon, P., Satre, V., Coutton, C., Jouk, P.‐S., Devillard, F., Dieterich, K., Afenjar, A., Burglen, L., Moutard, M.‐L., Addor, M.‐C., Lebon, S., Martinet, D., Alessandri, J.‐L., Doray, B., Miguet, M., Devys, D., Saugier‐Veber, P., Drunat, S., Aral, B., Kremer, V., Rondeau, S., Tabet, A.‐C., Thevenon, J., Thauvin‐Robinet, C., Perreton, N., Des Portes, V., Faivre, L.

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ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability von Mignot, Cyril, Moutard, Marie-Laure, Rastetter, Agnès, Boutaud, Lucile, Heide, Solveig, Billette, Thierry, Doummar, Diane, Garel, Catherine, Afenjar, Alexandra, Jacquette, Aurélia, Lacombe, Didier, Verloes, Alain, Bole-Feysot, Christine, Nitschké, Patrick, Masson, Cécile, Faudet, Anne, Lesne, Fabien, Bienvenu, Thierry, Alby, Caroline, Attié-Bitach, Tania, Depienne, Christel, Nava, Caroline, Héron, Delphine

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