Metformin Treatment Reduces CRC Aggressiveness in a Glucose-Independent Manner: An In Vitro and Ex Vivo Study by Boutaud, Marie, Auger, Clément, Verdier, Mireille, Christou, Niki

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Metformin Treatment Reduces CRC Aggressiveness in a Glucose-Independent Manner: An IIn Vitro/I and IEx Vivo/I Study by Boutaud, Marie, Auger, Clément, Verdier, Mireille, Christou, Niki

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Extracellular vesicles from type-2 macrophages increase the survival of chronic lymphocytic leukemia cells ex vivo by Ikhlef, Léa, Ratti, Nina, Durand, Stéphanie, Formento, Rémy, Daverat, Héloïse, Boutaud, Marie, Guillou, Clément, Dmytruk, Natalya, Gachard, Nathalie, Cosette, Pascal, Jauberteau, Marie-Odile, Gallet, Paul-François

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ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability by Mignot, Cyril, Moutard, Marie-Laure, Rastetter, Agnès, Boutaud, Lucile, Heide, Solveig, Billette, Thierry, Doummar, Diane, Garel, Catherine, Afenjar, Alexandra, Jacquette, Aurélia, Lacombe, Didier, Verloes, Alain, Bole-Feysot, Christine, Nitschké, Patrick, Masson, Cécile, Faudet, Anne, Lesne, Fabien, Bienvenu, Thierry, Alby, Caroline, Attié-Bitach, Tania, Depienne, Christel, Nava, Caroline, Héron, Delphine

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Expanding the phenotypic spectrum of LIG4 pathogenic variations: neuro-histopathological description of 4 fetuses with stenosis of the aqueduct by Nicolle, Romain, Boutaud, Lucile, Loeuillet, Laurence, Talhi, Naima, Grotto, Sarah, Bourgon, Nicolas, Feresin, Agnese, Coussement, Aurélie, Barrois, Mathilde, Beaujard, Marie-Paule, Rambaud, Thomas, Razavi, Férechté, Attié-Bitach, Tania

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Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU by Depienne, Christel, Nava, Caroline, Keren, Boris, Heide, Solveig, Rastetter, Agnès, Passemard, Sandrine, Chantot-Bastaraud, Sandra, Moutard, Marie-Laure, Agrawal, Pankaj B., VanNoy, Grace, Stoler, Joan M., Amor, David J., Billette de Villemeur, Thierry, Doummar, Diane, Alby, Caroline, Cormier-Daire, Valérie, Garel, Catherine, Marzin, Pauline, Scheidecker, Sophie, de Saint-Martin, Anne, Hirsch, Edouard, Korff, Christian, Bottani, Armand, Faivre, Laurence, Verloes, Alain, Orzechowski, Christine, Burglen, Lydie, Leheup, Bruno, Roume, Joelle, Andrieux, Joris, Sheth, Frenny, Datar, Chaitanya, Parker, Michael J., Pasquier, Laurent, Odent, Sylvie, Naudion, Sophie, Delrue, Marie-Ange, Le Caignec, Cédric, Vincent, Marie, Isidor, Bertrand, Renaldo, Florence, Stewart, Fiona, Toutain, Annick, Koehler, Udo, Häckl, Birgit, von Stülpnagel, Celina, Kluger, Gerhard, Møller, Rikke S., Pal, Deb, Jonson, Tord, Soller, Maria, Verbeek, Nienke E., van Haelst, Mieke M., de Kovel, Carolien, Koeleman, Bobby, Monroe, Glen, van Haaften, Gijs, Attié-Bitach, Tania, Boutaud, Lucile, Héron, Delphine, Mignot, Cyril

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Hydrothorax in fetal cases of Opitz G/BBB diagnosis: Extending the phenotype? by Tessier, Aude, Boutaud, Lucile, Bruel, Ange‐Line, Thauvin‐Robinet, Christel, Roth, Philippe, Malan, Valérie, Beaujard, Marie‐Paule, Achaiaa, Amale, Oliveira, Judite, Steffann, Julie, Encha‐Razavi, Ferechte, Faivre, Laurence, Bessières, Bettina, Attié‐Bitach, Tania

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Prognostic impact of high-intensity lipid-lowering therapy under-prescription after acute myocardial infarction in women by Weizman, Orianne, Hauguel-Moreau, Marie, Tea, Victoria, Albert, Franck, Barragan, Paul, Georges, Jean-Louis, Delarche, Nicolas, Kerneis, Mathieu, Bataille, Vincent, Drouet, Elodie, Puymirat, Etienne, Ferrières, Jean, Schiele, François, Simon, Tabassome, Danchin, Nicolas

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The first two non‐Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome by Ghesh, Leïla, Musquer, Marie Denis, Devisme, Louise, Stichelbout, Morgane, Boutaud, Lucile, Elkhartoufi, Nadia, Vaast, Pascal, Boute, Odile, Riteau, Anne‐Sophie, Le Vaillant, Claudine, Winer, Norbert, Joubert, Madeleine, Bezieau, Stéphane, Thomas, Sophie, Attie‐Bitach, Tania, Beneteau, Claire

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In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetuses by Alby, Caroline, Boutaud, Lucile, Bonnière, Maryse, Collardeau‐Frachon, Sophie, Guibaud, Laurent, Lopez, Estelle, Bruel, Ange‐Line, Aral, Bernard, Sonigo, Pascale, Roth, Philippe, Vibert‐Guigue, Claude, Castaigne, Vanina, Carbonne, Bruno, Joyé, Nicole, Faivre, Laurence, Cordier, Marie‐Pierre, Bernabe Gelot, Antoinette, Clementi, Maurizio, Mammi, Isabella, Vekemans, Michel, Razavi, Féréchté, Gonzales, Marie, Thauvin‐Robinet, Christel, Attié‐Bitach, Tania

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Clinical, chromosomal and molecular characterization of a cohort of 273 patients with agenesis of the corpus callosum by Heide, Solveig, Billette de Villemeur, Thierry, Nava, Caroline, Rastetter, Agnès, Mignot, Cyril, Depienne, Christel, Keren, Boris, Chantot-Bastaraud, Sandra, Attié-Bitach, Tania, Boutaud, Lucile, Afenjar, Alexandra, Whalen, Sandra, des Portes, Vincent, Faivre, Laurence, Toutain, Annick, Lacombe, Didier, Faudet, Anne, Garel, Catherine, Moutard, Marie-Laure, Héron, Delphine

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