An Unusual Giant Cell Tumor of the Thyroid: Case Report and Review of the Literature von Derbel, O, Zrounba, P, Chassagne-Clément, C, Decouvelaere, A. V, Orlandini, F, Duplomb, S, Blay, J. Y, de la Fouchardiere, C

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886P Retrospective multicentric survival analysis of patients receiving TPEx regimen (docetaxel, platinum and cetuximab) as first line treatment of recurrent or metastatic squamous... von Libert, L., Abdeddaim, C., Saleh, K., Even, C., Duplomb, S., Dubreuil, J., Rambeau, A., Guiard, E., Pointreau, Y., Olympios, N., Moldovan, C., Lévêque, E., Clatot, F.

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Journal de madame Rose de Saulces de Freycinet : campagne de "l'Uranie" (1817-1820) / d'après le manuscrit original, accompagné de notes par Charles Duplomb,.... Appartient à l’ens... von Freycinet, Rose de Saulces de (1794-1832). Auteur du texte

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Récits maritimes ou Lettres inédites de marins français / accompagnées de commentaires par Charles Duplomb,... ; préface du vice-amiral Bienaimé

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Journal de madame Rose de Saulces de Freycinet : campagne de "l'Uranie" (1817-1820) / d'après le manuscrit original, accompagné de notes par Charles Duplomb von Freycinet, Rose de Saulces de (1794-1832). Author of the text, Freycinet, Rose de Saulces de (1794-1832). Auteur du texte

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Récits maritimes ou Lettres inédites de marins français / accompagnées de commentaires par Charles Duplomb,... ; préface du vice-amiral Bienaimé

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Vps13b is required for acrosome biogenesis through functions in Golgi dynamic and membrane trafficking von Da Costa, Romain, Bordessoules, Morgane, Guilleman, Magali, Carmignac, Virginie, Lhussiez, Vincent, Courot, Hortense, Bataille, Amandine, Chlémaire, Amandine, Bruno, Céline, Fauque, Patricia, Thauvin, Christel, Faivre, Laurence, Duplomb, Laurence

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The dual role of IL-6-type cytokines on bone remodeling and bone tumors von Blanchard, Frédéric, Duplomb, Laurence, Baud’huin, Marc, Brounais, Bénédicte

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Homozygous FIBP nonsense variant responsible of syndromic overgrowth, with overgrowth, macrocephaly, retinal coloboma and learning disabilities von Thauvin-Robinet, C., Duplomb-Jego, L., Limoge, F., Picot, D., Masurel, A., Terriat, B., Champilou, C., Minot, D., St-Onge, J., Kuentz, P., Duffourd, Y., Thevenon, J., Rivière, J.-B., Faivre, L.

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Characterization of Vps13b-mutant mice reveals neuroanatomical and behavioral phenotypes with females less affected von Montillot, Charlotte, Skutunova, Emilia, Ayushma, Dubied, Morgane, Lahmar, Adam, Nguyen, Sylvie, Peerally, Benazir, Prin, Fabrice, Duffourd, Yannis, Thauvin-Robinet, Christel, Duplomb, Laurence, Wang, Heng, Ansar, Muhammad, Faivre, Laurence, Navarro, Nicolas, Minocha, Shilpi, Collins, Stephan C, Yalcin, Binnaz

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Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia von Thevenon, J., Duplomb, L., Phadke, S., Eguether, T., Saunier, A., Avila, M., Carmignac, V., Bruel, A.-L., St-Onge, J., Duffourd, Y., Pazour, G.J., Franco, B., Attie-Bitach, T., Masurel-Paulet, A., Rivière, J.-B., Cormier-Daire, V., Philippe, C., Faivre, L., Thauvin-Robinet, C.

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Analysis of the benefit of salvage chemotherapy after progression on nivolumab in patients with squamous cell carcinoma of the head and neck von Reverdy, Thibaut, Varnier, Romain, de Talhouët, Solène, Duplomb, Sophie, Bruyas, Amandine

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A first-in-class inhibitor of HSP110 to potentiate XPO1-targeted therapy in primary mediastinal B-cell lymphoma and classical Hodgkin lymphoma von Durand, Manon, Cabaud Gibouin, Vincent, Duplomb, Laurence, Salmi, Leila, Caillot, Mélody, Sola, Brigitte, Camus, Vincent, Jardin, Fabrice, Garrido, Carmen, Jego, Gaëtan

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Cetuximab, docetaxel, and cisplatin versus platinum, fluorouracil, and cetuximab as first-line treatment in patients with recurrent or metastatic head and neck squamous-cell carcin... von Guigay, Joël, Aupérin, Anne, Fayette, Jérôme, Lafond, Cédrik, Martin, Laurent, Capitain, Olivier, Cupissol, Didier, Even, Caroline, Sire, Christian, Duplomb, Sophie, Evrard, Camille, Delord, Jean-Pierre, Fraslin, Aldéric, Keilholz, Ulrich, Mesia, Ricard, BABA-HAMED, Nabil, BABIN, Emmanuel, BERA, Guillaume, BETRIAN-LAGARDE, Sarah, BLOT, Emmanuel, BOREL, Christian, BRUYAS, Amandine, CALAIS, Gilles, CARPIUC, Ioana, CHAPET, Sophie, CHATELLIER, Thierry, CHELI, Sandrine, CLATOT, Florian, COJOCARASU, Oana, COUTTE, Alexandre, DALLOZ, Pierre, DELHOMMEAU, Melissa, DE RAUCOURT, Dominique, DEBOURDEAU, Philippe, DUBOS-ARVIS, Catherine, DUCOULOMBIER, Agnès, EL KOURI, Claude, FALKOWSKI, Sabrina, FERRAND, François-Regis, GATINEAU, Michel, GERVAIS, Radj, GRAS, Louis, HASBINI, Ali, HENAULT, Stéphane, HERRERA GOMEZ, Ruth Gabriela, HUGUET, Florence, LAGRANGE, Aurélie, LE FOLL, Christine, LINOT, Benjamin, LOPEZ, Qian, MAYACHE-BADIS, Lamia, MINNE, Floriane, NEIDHARDT, Eve Marie, PAVILLET, Julien, PEYRADE, Frédéric, POINTREAU, Yohann, RAMEE, Jean-François, RAUCHE, Camille, RICHARD, Sandrine, RIZZO, Claudia, ROLLAND, Frédéric, STEFANI, Laetitia, TASSY, Louis, THERY, Jean-Christophe, TOULLEC, Clémence, TOURANI, Jean-Marc, TOUSSAINT, Philippe, VAULEON, Elodie, VIRET, Frédéric, WALER, Sabine, ATZPODIEN, Jens, FIETKAU, Rainer, GRANIZKA, Thordis, GUNTINAS-LICHINUS, Orlando, HADLER-MIKESCH, Kristina, HAHN, Dennis, INHESTERN, Johanna, KELLNER, Karolin, KLINGHAMMER, Konrad, KRONENBERGER, Roland, LUEDTKE-HECKENKAMP, Kerstin, OTREMBA, Burkhard, PIRLICH, Markus, ROTHMANN, Frank, TOMETTEN, Mareike, WOHLFARTH, Sabine, ZEBRALLA, Veit, ZIPFEL, Matthias, ADANSA KLEIN, Juan Carlos, ARRAZUBI, Virginia, CABALLERO DAROQUI, Javier, CASTELO, Beatriz, CIRAUQUI CIRAUQUI, Beatriz, GALLEGO, Oscar, IGLESIAS DOCAMPO, Lara Carmen, MARTINEZ DEL PRADO, Maria, MARTINEZ-TRUFERO, Javier, PASTOR BORGONON, Miguel, PEREZ RUIZ, Elisabeth, RUBIO CASADEVALL, Jordi

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Concise review: embryonic stem cells: a new tool to study osteoblast and osteoclast differentiation von Duplomb, Laurence, Dagouassat, Maylis, Jourdon, Philippe, Heymann, Dominique

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De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy von Tran Mau-Them, F., Guibaud, L., Duplomb, L., Keren, B., Lindstrom, K., Marey, I., Mochel, F., van den Boogaard, M. J., Oegema, R., Nava, C., Masurel, A., Jouan, T., Jansen, F. E., Au, M., Chen, Agnes H., Cho, M., Duffourd, Y., Lozier, E., Konovalov, F., Sharkov, A., Korostelev, S., Urteaga, B., Dickson, P., Vera, M., Martínez-Agosto, Julián A., Begemann, A., Zweier, M., Schmitt-Mechelke, T., Rauch, A., Philippe, C., van Gassen, K., Nelson, S., Graham, J. M., Friedman, J., Faivre, L., Lin, H. J., Thauvin-Robinet, C., Vitobello, A.

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In-Frame Mutations in Exon 1 of SKI Cause Dominant Shprintzen-Goldberg Syndrome von CARMIGNAC, Virginie, THEVENON, Julien, RENARD, Marjolijn, PLAUCHU, Henri, PLESSIS, Ghislaine, DE BACKER, Julie, CHILD, Anne, ARNO, Gavin, DUPLOMB, Laurence, CALLIER, Patrick, ARAL, Bernard, VABRES, Pierre, ADES, Lesley, GIGOT, Nadege, ARBUSTINI, Eloisa, GRASSO, Maurizia, ROBINSON, Peter N, GOIZET, Cyril, BAUMANN, Clarisse, DI ROCCO, Maja, DEL POZO, Jaime Sanchez, HUET, Frédéric, JONDEAU, Guillaume, CALLEWAERT, Bert, COLLOD-BEROUD, Gwenaelle, BEROUD, Christophe, AMIEL, Jeanne, CORMIER-DAIRE, Valérie, RIVIERE, Jean-Baptiste, BOILEAU, Catherine, DE PAEPE, Anne, FAIVRE, Laurence, JULIA, Sophie, THAUVIN-ROBINET, Christel, GUENEAU, Lucie, COURCET, Jean-Benoit, LOPEZ, Estelle, HOLMAN, Katherine

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Haploinsufficiency of ARFGEF1 is associated with developmental delay, intellectual disability, and epilepsy with variable expressivity von Thomas, Quentin, Gautier, Thierry, Marafi, Dana, Besnard, Thomas, Willems, Marjolaine, Moutton, Sébastien, Isidor, Bertand, Cogné, Benjamin, Conrad, Solène, Tenconi, Romano, Iascone, Maria, Sorlin, Arthur, Masurel, Alice, Dabir, Tabib, Jackson, Adam, Banka, Siddharth, Delanne, Julian, Lupski, James R., Saadi, Nebal Waill, Alkuraya, Fowzan S., Zahrani, Fatema Al, Agrawal, Pankaj B., England, Eleina, Madden, Jill A., Posey, Jennifer E., Burglen, Lydie, Rodriguez, Diana, Chevarin, Martin, Nguyen, Sylvie, Mau-Them, Frédéric Tran, Duffourd, Yannis, Garret, Philippine, Bruel, Ange-Line, Callier, Patrick, Marle, Nathalie, Denomme-Pichon, Anne-Sophie, Duplomb, Laurence, Philippe, Christophe, Thauvin-Robinet, Christel, Govin, Jérôme, Faivre, Laurence, Vitobello, Antonio

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Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy von Gabrielle, Pierre-Henry, Faivre, Laurence, Audo, Isabelle, Zanlonghi, Xavier, Dollfus, Hélène, Thiadens, Alberta A. H. J., Zeitz, Christina, Mancini, Grazia M. S., Perdomo, Yaumara, Mohand-Saïd, Saddek, Lizé, Eléonore, Lhussiez, Vincent, Nandrot, Emeline F., Acar, Niyazi, Creuzot-Garcher, Catherine, Sahel, José-Alain, Ansar, Muhammad, Thauvin-Robinet, Christel, Duplomb, Laurence, Da Costa, Romain

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Osteoprotegerin: Multiple partners for multiple functions von Baud’huin, Marc, Duplomb, Laurence, Teletchea, Stéphane, Lamoureux, François, Ruiz-Velasco, Carmen, Maillasson, Mike, Redini, Françoise, Heymann, Marie-Françoise, Heymann, Dominique

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