IgE detection in allergic patient's serum by absorption analysis of biofunctionalised microparticles von Yescas González, Tonatiuh, Leonard, Anthony, Gaude, Victor, Delplanque, Alexandra, Barre, Annick, Rougé, Pierre, Garnier, Lorna, Bienvenu, Françoise, Bienvenu, Jacques, Zelsmann, Marc, Picard, Emmanuel, Peyrade, David

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Bases moleculaires de la réactivité croisée entre Act c 12 et les allergènes globulines 11S des graines : identification in silico des épitopes B d’Act c 12 von Barre, Annick, Delplanque, Alexandra, Simplicien, Mathias, Benoist, Hervé, Rougé, Pierre

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Sécurité du maïs pour les patients souffrant de maladie cœliaque ? von Barre, A., Delplanque, A., Simplicien, M., Benoist, H., Rougé, P.

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Les allergènes croisants des insectes comestibles von Barre, A., Velazquez, E., Delplanque, A., Caze-Subra, S., Bienvenu, F., Bienvenu, J., Benoist, H., Rougé, P.

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Fotografisk reproduktionsapparat med en understøtningsplade for et lysfølsomt papirark under eksponeringen og et endeløst transportbånd von MARCEL LOUIS ALEXANDRA DELPLANQUE

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Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations von Froguel, Philippe, Lobbens, Stéphane, Elliott, Paul, Sladek, Rob, Levy-Marchal, Claire, Balkau, Beverley, Polychronakos, Constantin, Gallina, Sophie, Proença, Christine, Meyre, David, Vatin, Vincent, Delplanque, Jérôme, Potoczna, Natascha, Kovacs, Peter, Tauber, Maithé, Järvelin, Marjo-Riitta, Marre, Michel, Weill, Jacques, Walley, Andrew, Degraeve, Franck, Horber, Fritz, Hercberg, Serge, Tichet, Jean, Coin, Lachlan J M, Dina, Christian, Körner, Antje, Lecoeur, Cécile, Hartikainen, Anna-Liisa, Asher, Julian, McCarthy, Mark I, Montpetit, Alexandre, Gaget, Stefan, Durand, Emmanuelle, Balding, David, Heude, Barbara, Blakemore, Alexandra I F, Kiess, Wieland, Pattou, François, Chèvre, Jean-Claude, Visvikis-Siest, Sophie

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A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk von Chèvre, Jean-Claude, Pedersen, Oluf, Walley, Andrew J, Elliott, Paul, Sparsø, Thomas, Marre, Michel, Charpentier, Guillaume, Rocheleau, Ghislain, Pattou, François, Blakemore, Alexandra I F, Jarvelin, Marjo-Riita, Vaxillaire, Martine, Heude, Barbara, Bouatia-Naji, Nabila, Balkau, Beverley, Hartikainen, Anna-Liisa, De Graeve, Franck, Dina, Christian, Lobbens, Stéphane, Borch-Johnsen, Knut, Weill, Jacques, Schuit, Frans, Ruokonen, Aimo, Tauber, Maithé, Sladek, Robert, Delplanque, Jérôme, Cavalcanti-Proença, Christine, Meyre, David, Holmkvist, Johan, Hadjadj, Samy, Jørgensen, Torben, Durand, Emmanuelle, Marchand, Marion, Lévy-Marchal, Claire, Bonnefond, Amélie, Cauchi, Stéphane, Visvikis-Siest, Sophie, Hansen, Torben, Froguel, Philippe, Tichet, Jean, Lemaire, Katleen

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TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment von DELPLANQUE, Jérôme, DEVOS, David, BUEE, Luc, DESTEE, Alain, GROLEZ, Guillaume, DELMAIRE, Christine, DUJARDIN, Kathy, DELLACHERIE, Delphine, BRICE, Alexis, STEVANIN, Giovanni, STRUBI-VUILLAUME, Isabelle, DÜRR, Alexandra, HUIN, Vincent, SABLONNIERE, Bernard, GENET, Alexandre, SAND, Olivier, MOREAU, Caroline, GOIZET, Cyril, CHARLES, Perrine, ANHEIM, Mathieu, MONIN, Marie Lorraine

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A Rare Variant in the Visfatin Gene ( ) Is Associated With Protection From Obesity von Blakemore, Alexandra I.F., Meyre, David, Delplanque, Jerome, Vatin, Vincent, Lecoeur, Cecile, Marre, Michel, Tichet, Jean, Balkau, Beverley, Froguel, Philippe, Walley, Andrew J.

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A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk von Bouatia-Naji, Nabila, Bonnefond, Amelie, Cavalcanti-Proenca, Christine, Sparso, Thomas, Holmkvist, Johan, Marchand, Marion, Delplanque, Jerome, Lobbens, Stephane, Rocheleau, Ghislain, Durand, Emmanuelle, De Graeve, Franck, Chevre, Jean-Claude, Borch-Johnsen, Knut, Hartikainen, Anna-Liisa, Ruokonen, Aimo, Tichet, Jean, Marre, Michel, Weill, Jacques, Heude, Barbara, Tauber, Maithe, Lemaire, Katleen, Schuit, Frans, Elliott, Paul, Jorgensen, Torben, Charpentier, Guillaume, Hadjadj, Samy, Cauchi, Stephane, Vaxillaire, Martine, Sladek, Robert, Visvikis-Siest, Sophie, Balkau, Beverley, Levy-Marchal, Claire, Pattou, Francois, Meyre, David, Blakemore, Alexandra I.F, Jarvelin, Marjo-Riita, Walley, Andrew J, Hansen, Torben, Dina, Christian, Pedersen, Oluf, Froguel, Philippe

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TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment von Delplanque, Jérôme, Devos, David, Huin, Vincent, Genet, Alexandre, Sand, Olivier, Moreau, Caroline, Goizet, Cyril, Perrine, Charles, Anheim, Mathieu, Monin, Marie Lorraine, Buée, Luc, Destée, Alain, Grolez, Guillaume, Delmaire, Christine, Dujardin, Kathy, Dellacherie, Delphine, Brice, Alexis, Stevanin, Giovanni, Strubi-Vuillaume, Isabelle, Durr, Alexandra, Sablonnière, Bernard

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