sistema de baliza de emergência automática von CAROLE FLOQUET-PICARD, THIERRY PORTES, ALAIN CAVAN, CLAUDE CRESP

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Distress beacon system for an aircraft or another vehicle von Portes Thierry, Cresp Claude, Floquet-Picard Carole, Cavan Alain

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DISTRESS BEACON SYSTEM FOR AN AIRCRAFT OR ANOTHER VEHICLE von PORTES, Thierry, CRESP, Claude, FLOQUET-PICARD, Carole, CAVAN, Alain

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DISTRESS BEACON SYSTEM FOR AN AIRCRAFT OR ANOTHER VEHICLE von CAVAN ALAIN, CRESP CLAUDE, PORTES THIERRY, FLOQUET-PICARD CAROLE

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DISTRESS BEACON SYSTEM FOR AN AIRCRAFT OR ANOTHER VEHICLE von CAVAN, ALAIN, PORTES, THIERRY, FLOQUET-PICARD, CAROLE, CRESP, CLAUDE

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Distress beacon system for an aircraft or another vehicle von CAVAN ALAIN, CRESP CLAUDE, PORTES THIERRY, FLOQUET-PICARD CAROLE

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SYSTEME DE BALISE DE DETRESSE POUR AERONEF OU AUTRE VEHICULE von CAVAN ALAIN, CRESP CLAUDE, PORTES THIERRY, FLOQUET-PICARD CAROLE

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Sistema de baliza de socorro para aeronave u otro vehículo von PORTES, Thierry, CRESP, Claude, FLOQUET-PICARD, Carole, CAVAN, Alain

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DISTRESS BEACON SYSTEM FOR AN AIRCRAFT OR ANOTHER VEHICLE von CAVAN, ALAIN, PORTES, THIERRY, FLOQUET-PICARD, CAROLE, CRESP, CLAUDE

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DISTRESS BEACON SYSTEM FOR AN AIRCRAFT OR ANOTHER VEHICLE von CAVAN, ALAIN, PORTES, THIERRY, FLOQUET-PICARD, CAROLE, CRESP, CLAUDE

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SYSTEME DE BALISE DE DETRESSE POUR AERONEF OU AUTRE VEHICULE von CAVAN ALAIN, CRESP CLAUDE, PORTES THIERRY, FLOQUET-PICARD CAROLE

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Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly von Poirier, Karine, Lebrun, Nicolas, Broix, Loic, Tian, Guoling, Saillour, Yoann, Boscheron, Cécile, Parrini, Elena, Valence, Stephanie, Pierre, Benjamin Saint, Oger, Madison, Lacombe, Didier, Geneviève, David, Fontana, Elena, Darra, Franscesca, Cances, Claude, Barth, Magalie, Bonneau, Dominique, Bernadina, Bernardo Dalla, N'Guyen, Sylvie, Gitiaux, Cyril, Parent, Philippe, des Portes, Vincent, Pedespan, Jean Michel, Legrez, Victoire, Castelnau-Ptakine, Laetitia, Nitschke, Patrick, Hieu, Thierry, Masson, Cecile, Zelenika, Diana, Andrieux, Annie, Francis, Fiona, Guerrini, Renzo, Cowan, Nicholas J, Bahi-Buisson, Nadia, Chelly, Jamel

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Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient von Burglen, Lydie, Chantot-Bastaraud, Sandra, Garel, Catherine, Milh, Mathieu, Touraine, Renaud, Zanni, Ginevra, Petit, Florence, Afenjar, Alexandra, Goizet, Cyril, Barresi, Sabina, Coussement, Aurélie, Ioos, Christine, Lazaro, Leila, Joriot, Sylvie, Desguerre, Isabelle, Lacombe, Didier, des Portes, Vincent, Bertini, Enrico, Siffroi, Jean-Pierre, de Villemeur, Thierry Billette, Rodriguez, Diana

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KCNT1 epilepsy with migrating focal seizures shows a temporal sequence with poor outcome, high mortality and SUDEP von Kuchenbuch, Mathieu, Barcia, Giulia, Chemaly, Nicole, Carme, Emilie, Roubertie, Agathe, Gibaud, Marc, Van Bogaert, Patrick, de Saint Martin, Anne, Hirsch, Edouard, Dubois, Fanny, Sarret, Catherine, Nguyen The Tich, Sylvie, Laroche, Cecile, des Portes, Vincent, Billette de Villemeur, Thierry, Barthez, Marie-Anne, Auvin, Stéphane, Bahi-Buisson, Nadia, Desguerre, Isabelle, Kaminska, Anna, Benquet, Pascal, Nabbout, Rima

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Movement disorders in patients with alternating hemiplegia: “Soft” and “stiff” at the same time von Panagiotakaki, Eleni, Doummar, Diane, Nogue, Erika, Nagot, Nicolas, Lesca, Gaetan, Riant, Florence, Nicole, Sophie, Delaygue, Charlene, Barthez, Marie Anne, Nassogne, Marie Cécile, Dusser, Anne, Vallée, Louis, Billette, Thierry, Bourgeois, Marie, Ioos, Christine, Gitiaux, Cyril, Laroche, Cécile, Milh, Mathieu, Portes, Vincent Des, Arzimanoglou, Alexis, Roubertie, Agathe

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Voice Quality and Gender Stereotypes: A Study of Lebanese Women with Reinke's Edema von Matar, Nayla, Portes, Cristel, Lancia, Leonardo, Legou, Thierry, Baider, Fabienne

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The three stages of epilepsy in patients with CDKL5 mutations von Bahi‐Buisson, Nadia, Kaminska, Anna, Boddaert, Nathalie, Rio, Marlène, Afenjar, Alexandra, Gérard, Marion, Giuliano, Fabienne, Motte, Jacques, Héron, Delphine, Morel, Marie Ange N'Guyen, Plouin, Perrine, Richelme, Christian, Des Portes, Vincent, Dulac, Olivier, Philippe, Christophe, Chiron, Catherine, Nabbout, Rima, Bienvenu, Thierry

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New insights into genotype―phenotype correlations for the doublecortin-related lissencephaly spectrum von BAHI-BUISSON, Nadia, SOUVILLE, Isabelle, LOUIS LEGER, Pierre, ELIE, Caroline, BODDAERT, Nathalie, BELDJORD, Cherif, CHELLY, Jamel, FRANCIS, Fiona, EUROPEAN CONSORTIUM, Sbh-Lis, FOURNIOL, Franck J, TOUSSAINT, Aurelie, MOORES, Carolyn A, HOUDUSSE, Anne, YVES LEMAITRE, Jean, POIRIER, Karine, KHALAF-NAZZAL, Reham, HULLY, Marie

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MECP2 is highly mutated in X-linked mental retardation von COUVERT, Philippe, BIENVENU, Thierry, STEFFANN, Julie, DES PORTES, Vincent, ROPERS, Hans-Hilger, YNTEMA, Helger G, FRYNS, Jean-Pierre, BRIAULT, Sylvain, CHELLY, Jamel, CHERIF, Beldjord, AQUAVIVA, Cecile, POIRIER, Karine, MORA, Claude, GENDROT, Chantal, VERLOES, Alain, ANDRES, Christian, LE FEVRE, Anne Celine, SOUVILLE, Isabelle

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Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation von Billuart, Pierre, Bienvenu, Thierry, Ronce, Nathalie, des Portes, Vincent, Vinet, Marie Claude, Zemni, Ramzi, Crollius, Hugues Roest, Carrié, Alain, Fauchereau, Fabien, Cherry, Michele, Briault, Sylvain, Hamel, Ben, Fryns, Jean-Pierre, Beldjord, Cherif, Kahn, Axel, Moraine, Claude, Chelly, Jamel

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