Inhibition of the mTORC Pathway in the Antiphospholipid Syndrome von Canaud, Guillaume, Bienaimé, Frank, Tabarin, Fanny, Bataillon, Guillaume, Seilhean, Danielle, Noël, Laure-Hélène, Dragon-Durey, Marie-Agnès, Snanoudj, Renaud, Friedlander, Gérard, Halbwachs-Mecarelli, Lise, Legendre, Christophe, Terzi, Fabiola

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Complement Factor B Mutations in Atypical Hemolytic Uremic Syndrome—Disease-Relevant or Benign? von MARINOZZI, Maria Chiara, VERGOZ, Laura, SMITH, Richard J, NORIS, Marina, HALBWACHS-MECARELLI, Lise, DONADELLI, Roberta, FREMEAUX-BACCHI, Veronique, ROUMENINA, Lubka T, RYBKINE, Tania, NGO, Stephanie, BETTONI, Serena, PASHOV, Anastas, CAYLA, Mathieu, TABARIN, Fanny, JABLONSKI, Mathieu, HUE, Christophe

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M-ficolin and leukosialin (CD43): new partners in neutrophil adhesion von Andrea N. Moreno-Amaral, Evelyne Gout, Claudia Danella-Polli, Fanny Tabarin, Philippe Lesavre, Gabriela Pereira-da-Silva, Nicole M. Thielens, Lise Halbwachs-Mecarelli

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Complement activation by heme as a secondary hit for atypical hemolytic uremic syndrome von Frimat, Marie, Tabarin, Fanny, Dimitrov, Jordan D., Poitou, Caroline, Halbwachs-Mecarelli, Lise, Fremeaux-Bacchi, Veronique, Roumenina, Lubka T.

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Dynamics of cell adhesion on fluid substrates von Mikhajlov, Oleg, Di Federico, Fahima, Manzi, John, Tabarin, Fanny, van Nhieu, Guy Tran, Bassereau, Patricia M.

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Cell adhesion and spreading on fluid membranes through microtubules-dependent mechanotransduction von Mikhajlov, Oleg, Adar, Ram, Tătulea-Codrean, Maria, Macé, Anne-Sophie, Manzi, John, Tabarin, Fanny, Battistella, Aude, Di Federico, Fahima, Joanny, Jean-François, van Nhieu, Guy Tran, Bassereau, Patricia

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Free heme transforms endothelial cells into alternative pathway activators. Implications for the hemolytic and uremic syndrome von Frimat, Marie, Tabarin, Fanny, Halbwachs, Lise, Poitou, Caroline, Dimitrov, Jordan, Fremeaux-Bacchi, Veronique, Roumenina, Lubka

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Membrane cofactor protein (MCP) haplotype, which predisposes to atypical hemolytic and uremic syndrome, has no consequence on neutrophils and endothelial cells MCP levels or on HUV... von frimat, Marie, Roumenina, Lubka T, Tabarin, Fanny, Halbwachs-Mecarelli, Lise, Fremeaux-Bacchi, Veronique

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Diabetes insipidus: Vasopressin deficiency von Chasseloup, Fanny, Tabarin, Antoine, Chanson, Philippe

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Loss of KDM1A in GIP-dependent primary bilateral macronodular adrenal hyperplasia with Cushing's syndrome: a multicentre, retrospective, cohort study von Chasseloup, Fanny, Bourdeau, Isabelle, Tabarin, Antoine, Regazzo, Daniela, Dumontet, Charles, Ladurelle, Nataly, Tosca, Lucie, Amazit, Larbi, Proust, Alexis, Scharfmann, Raphael, Mignot, Tiphaine, Fiore, Frédéric, Tsagarakis, Stylianos, Vassiliadi, Dimitra, Maiter, Dominique, Young, Jacques, Lecoq, Anne-Lise, Deméocq, Vianney, Salenave, Sylvie, Lefebvre, Hervé, Cloix, Lucie, Emy, Philippe, Dessailloud, Rachel, Vezzosi, Delphine, Scaroni, Carla, Barbot, Mattia, de Herder, Wouter, Pattou, François, Tétreault, Martine, Corbeil, Gilles, Dupeux, Margot, Lambert, Benoit, Tachdjian, Gérard, Guiochon-Mantel, Anne, Beau, Isabelle, Chanson, Philippe, Viengchareun, Say, Lacroix, André, Bouligand, Jérôme, Kamenický, Peter

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OR04-4 Loss of KDM1A in Bilateral Macronodular Adrenal Hyperplasia With GIP-Dependent Cushing's Syndrome and in Acromegaly With Paradoxical GH Response to Oral Glucose von Amazit, Larbi, Barbot, Mattia, Beau, Isabelle, Bouligand, Jérôme, Bourdeau, Isabelle, Chanson, Philippe, Cloix, Lucie, Corbeil, Gilles, de Herder, Wouter, Deméocq, Vianney, Desailloud, Rachel, Dumontet, Charles, Dupeux, Margot, Emy, Philippe, Fiore, Frederic, Guiochon-Mantel, Anne, Kamenicky, Peter, Lacroix, André, Ladurelle, Nataly, Lambert, Benoit, Lecoq, Anne-Lise, Lefebvre, Hervé, Maiter, Dominique, Pattou, Francois, Proust, Alexis, Regazzo, Daniela, Salenave, Sylvie, Scaroni, Carla, Scharfmann, Raphael, Tabarin, Antoine, Tachdjian, Gerard, Tetreault, Martine, Tosca, Lucie, Tsagarakis, Stylianos, Vassiliadi, Dimitra, Vezzosi, Delphine, Viengchareun, Say, Young, Jacques, Chasseloup, Fanny

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Pénétrance de l’hyperplasie macronodulaire bilatérale des surrénales GIP-dépendante avec syndrome de Cushing chez les porteurs de mutations de KDM1A von Chasseloup, F., Cloix, L., Nunes, M.L., Galliot, P., Richa, C., Herrou, A.F., Salenave, S., Ait-Tayeb, A.E.K., Galioot, A., Meyrignac, O., Barbot, M., Regazzo, D., Maiter, D., Tsagarakis, S., Desailloud, R., Emy, P., Bourdeau, I., Lacroix, A., Nocturne, G., Trabado, S., Young, J., Tabarin, A., Bouligand, J., Kamenicky, P.

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