Lateralization of prefrontal activation during internal mental calculation: a functional magnetic resonance imaging study von Burbaud, P, Degreze, P, Lafon, P, Franconi, J. M, Bouligand, B, Bioulac, B, Caille, J. M, Allard, M

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Error assessment due to coronary stents in flow-encoded phase contrast MR angiography: a phantom study von Lethimonnier, F., Bouligand, B., Thouveny, F., Furber, A., Jallet, P., Caron-Poitreau, C., Le Jeune, J.J.

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Differential prefrontal and parietal activation in numeric working memory and calculation procedures: a functional magnetic resonance imaging study von Burbaud, P., Müller, E., Guehl, D., Franconi, J.M., Degrèze, P., Lafon, P., Bouligand, B., Bioulac, B., Caillé, J.M., Allard, M.

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In vivo 13C chemical shift imaging of the human liver von Thiaudière, E., Biran, M., Delalande, C., Bouligand, B., Canioni, P.

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Les échos von Bouligand, B.

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Macroprolactinomas in Children and Adolescents: Factors Associated With the Response to Treatment in 77 Patients von Salenave, Sylvie, Ancelle, Deborah, Bahougne, Thibaut, Raverot, Gérald, Kamenický, Peter, Bouligand, Jérôme, Guiochon-Mantel, Anne, Linglart, Agnès, Souchon, Pierre-François, Nicolino, Marc, Young, Jacques, Borson-Chazot, Françoise, Delemer, Brigitte, Chanson, Philippe

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Significant prevalence of NR3C1 mutations in incidentally discovered bilateral adrenal hyperplasia: results of the French MUTA-GR Study von Vitellius, Géraldine, Trabado, Séverine, Hoeffel, Christine, Bouligand, Jérôme, Bennet, Antoine, Castinetti, Frederic, Decoudier, Bénédicte, Guiochon-Mantel, Anne, Lombes, Marc, Delemer, Brigitte

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NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency von Bouali, N., Francou, B., Bouligand, J., Lakhal, B., Malek, I., Kammoun, M., Warszawski, J., Mougou, S., Saad, A., Guiochon-Mantel, A.

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The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres von Persani, Luca, Cools, Martine, Ioakim, Stamatina, Faisal Ahmed, S, Andonova, Silvia, Avbelj-Stefanija, Magdalena, Baronio, Federico, Bouligand, Jerome, Bruggenwirth, Hennie T, Davies, Justin H, De Baere, Elfride, Dzivite-Krisane, Iveta, Fernandez-Alvarez, Paula, Gheldof, Alexander, Giavoli, Claudia, Gravholt, Claus H, Hiort, Olaf, Holterhus, Paul-Martin, Juul, Anders, Krausz, Csilla, Lagerstedt-Robinson, Kristina, McGowan, Ruth, Neumann, Uta, Novelli, Antonio, Peyrassol, Xavier, Phylactou, Leonidas A, Rohayem, Julia, Touraine, Philippe, Westra, Dineke, Vezzoli, Valeria, Rossetti, Raffaella

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The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening von Thauvin-Robinet, C, Munck, A, Huet, F, Génin, E, Bellis, G, Gautier, E, Audrézet, M-P, Férec, C, Lalau, G, Georges, M Des, Claustres, M, Bienvenu, T, Gérard, B, Boisseau, P, Cabet-Bey, F, Feldmann, D, Clavel, C, Bieth, E, Iron, A, Simon-Bouy, B, Costa, C, Medina, R, Leclerc, J, Hubert, D, Nové-Josserand, R, Sermet-Gaudelus, I, Rault, G, Flori, J, Leroy, S, Wizla, N, Bellon, G, Haloun, A, Perez-Martin, S, d’Acremont, G, Corvol, H, Clément, A, Houssin, E, Binquet, C, Bonithon-Kopp, C, Alberti-Boulmé, C, Morris, M A, Faivre, L, Goossens, M, Roussey, M

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Hypogonadisme hypogonadotrophique (HH) par mutations de PNPLA6 : découverte d’un spectre phénotypique plus large et corrélations fonctionnelles avec l’activité NTE in vitro... von Maione, L., Bouligand, J., Li, C., Rousseau, A., Prevost, S., Francou, B., Salenave, S., Chanson, P., Kaiser, U., Young, J.

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Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility von Guediche, N, Tosca, L, Kara Terki, A, Bas, C, Lecerf, L, Young, J, Briand-Suleau, A, Tou, B, Bouligand, J, Brisset, S, Misrahi, M, Guiochon-Mantel, A, Goossens, M, Tachdjian, G

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Étude par Exome chez 401 patients avec hypogonadisme hypogonadotrohique congénital (HHC) révèle des architectures génétiques différentes chez ceux avec Kallmann (SK) versus des HHC... von Bouligand, J., Chappell, K., Maione, L., Proust, A., Francou, B., Guiochon-Mantel, A., Young, J.

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OC7 Maralixibat-treated patients with Alagille syndrome demonstrate event-free survival in a natural history comparison with patients with from the GALA database: application of re... von Hansen, B E, Vandriel, S M, Vig, P, Garner, W, Mogul, D B, Loomes, K M, Piccoli, DA, Rand, E B, Jankowska, I, Czubkowski, P, Gliwicz-Miedzińska, D, Gonzales, E M, Jacquemin, E, Bouligand, J, L D’Antiga, Nicastro, E, Arnell, H, Fischler, B, Sokal, É, Demaret, T, Siew, S, Stormon, M, Karpen, S J, Romero, R, Ebel, N H, Feinstein, JA, Roberts, A J, Evans, H M, Sundaram, S S, Chaidez, A, Hardikar, W, Shankar, S, Fischer, R T, Lacaille, F, Debray, D, Lin, H C, Jensen, M K, Jaramillo, C, Karthikeyan, P, Indolfi, G, Verkade, HJ, Larson-Nath, C, Quiros-Tejeira, R E, Valentino, P L, Rogalidou, M, Dezsőfi, A, Squires, JE, Schwarz, K, Calvo, P L, J Quintero Bernabeu, Zizzo, AN, Nebbia, G, Bulut, P, Santos-Silva, E, Fawaz, R, Nastasio, S, Karnsakul, W, M Legarda Tamara, C Molera Busoms, Kelly, D, T Damgaard Sandahl, Jimenez-Rivera, C, Banales, JM, Mujawar, Q, Li, L T, She, H, Wang, J S, Kim, K M, Oh, SH, Sanchez, M C, Cavalieri, M L, Lee, W S, Hajinicolaou, C, Lertudomphonwanit, C, Waisbourd-Zinman, O, Arikan, C, Alam, S, Carvalho, E, Melere, M, Eshun, J, Önal, Z, Desai, D M, Wiecek, S, Pinto, R B, Wolters, V M, Garcia, J, Beretta, M, Kerkar, N, Brecelj, J, Rock, N, Lurz, E, Blondet, N, Shah, U, Thompson, R J, Kamath, B M

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SALL4 and NFATC2 : Two major actors of interstitial 20q13.2 duplication von Briand-Suleau, A, Martinovic, J, Tosca, L, Tou, B, Brisset, S, Bouligand, J, Delattre, V, Giurgea, I, Bachir, J, Folliot, P, Goumy, C, Francannet, C, Guiochon-Mantel, A, Benachi, A, Vermeesch, J, Tachdjian, G, Vago, P, Goossens, M, Métay, C

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Chemists and the school of nature von Bensaude-Vincent, Bernadette, Arribart, Hervé, Bouligand, Yves, Sanchez, Clément

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CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders von Thauvin-Robinet, Christel, Munck, Anne, Huet, Frédéric, de Becdelièvre, Alix, Jimenez, Clément, Lalau, Guy, Gautier, Elodie, Rollet, Jacques, Flori, Jean, Nové-Josserand, Raphaëlle, Soufir, Jean-Claude, Haloun, Alain, Hubert, Dominique, Houssin, Elise, Bellis, Gil, Rault, Gilles, David, Albert, Janny, Laurent, Chiron, Raphaël, Rives, Nathalie, Hairion, Dominique, Collignon, Patrick, Valeri, Antoine, Karsenty, Gilles, Rossi, Annick, Audrézet, Marie-Pierre, Férec, Claude, Leclerc, Julie, Georges, Marie des, Claustres, Mireille, Bienvenu, Thierry, Gérard, Bénédicte, Boisseau, Pierre, Cabet-Bey, Faïza, Cheillan, David, Feldmann, Delphine, Clavel, Christine, Bieth, Eric, Iron, Albert, Simon-Bouy, Brigitte, Izard, Vincent, Steffann, Julie, Viville, Stéphane, Costa, Catherine, Drouineaud, Véronique, Fauque, Patricia, Binquet, Christine, Bonithon-Kopp, Claire, Morris, Mike A, Faivre, Laurence, Goossens, Michel, Roussey, Michel, Girodon, Emmanuelle

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Conséquence de la perte fonctionnelle de la lysine déméthylase KDM1A sur la méthylation des histones, la conformation chromatinienne et expression génique dans l’hyperplasie macron... von Chasseloup, F., Syx, L., Ancelin, K., Ladurelle, N., Amazit, L., Fiore, F., Lambert, B., Viengchareun, S., Cloix, L., Nunes, M.L., Galioot, A., Barbot, M., Regazzo, D., Scaroni, C., Pattou, F., Maiter, D., Tsagarakis, S., Desailloud, R., Emy, P., Bourdeau, I., Lacroix, A., Lefebvre, H., Young, J., Tabarin, A., Bouligand, J., Servant, N., Kamenicky, P.

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APPLICATION OF REAL-WORLD EVIDENCE ANALYTICS: A 6-YEAR EVENT-FREE SURVIVAL ANALYSIS IN ALAGILLE SYNDROME OF THE GALA CLINICAL RESEARCH DATABASE AND MARALIXIBAT TREATED PATIENTS von Hansen, BE, Vandriel, SM, Vig, P, Garner, W, Li, LT, She, H, Wang, JS, Gilbert, MA, Jankowska, I, Czubkowski, P, Gliwicz-Miedzinska, D, Gonzales, EM, Jacquemin, E, Bouligand, J, Spinner, N, Loomes, KM, Piccoli, DA, D'Antiga, L, Nicastro, E, Sokal, E, Demaret, T, Ebel, N, Feinstein, JA, Fawaz, R, Nastasio, S, Lacaille, F, Debray, D, Arnell, H, Fischler, B, Siew, S, Stormon, M, Karpen, SJ, Romero, R, Kim, KM, Baek, WY, Hardikar, W, Shankar, S, Roberts, AJ, Evans, HM, Jensen, MK, Kavan, M, Sundaram, SS, Chaidez, A, Karthikeyan, P, Davison, S, Sanchez, MC, Cavalieri, ML, Verkade, HJ, Lee, WS, Squires, JE, Hajinicolaou, C, Lertudomphonwanit, C, Fischer, RT, Larson-Nath, C, Mozer-Glassberg, Y, Arikan, C, Lin, HC, Bernabeu, JQ, Alam, S, Kelly, D, Carvalho, E, Ferreira, CT, Indolfi, G, Quiros-Tejeira, RE, Bulut, P, Calvo, PL, Onal, Z, Valentino, PL, Desai, DM, Eshun, J, Rogalidou, M, Dezsofi, A, Wiecek, S, Nebbia, G, Pinto, RB, Wolters, VM, Tamara, ML, Zizzo, AN, Garcia, J, Schwarz, K, Beretta, M, Sandahl, TD, Jimenez-Rivera, C, Kerkar, N, Brecelj, J, Mujawar, Q, Rock, N, Molera, C, Karnsakul, W, Lurz, E, Santos-Silva, E, Blondet, N, Bujanda, L, Shah, U, Thompson, RJ, Kamath, BM

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La perte de la lysine demethylase KDM1A est la cause de l’hyperplasie macronodulaire bilatérale des surrénales GIP-dépendante von Chasseloup, F., Bourdeau, I., Tabarin, A., Regazzo, D., Dumontet, C., Ladurelle, N., Tosca, L., Amazit, L., Proust, A., Scharfmann, R., Fiore, F., Tsagarakis, S., Vassiliadi, D., Maiter, D., Young, J., Lecoq, A.L., Demeocq, V., Salenave, S., Lefebvre, H., Cloix, L., Emy, P., Desailloud, R., Vezzosi, D., Scaroni, C., Barbot, M., De Herder, W., Pattou, F., Tetreault, M., Corbeil, G., Dupeux, M., Lambert, B., Tachdjian, G., Guiochon-Mantel, A., Beau, I., Chanson, P., Viengchareun, S., Lacroix, A., Bouligand, J., Kamenicky, P.

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