A new electrolytic pencil for the local cleaning of silver tarnish von Degrigny, Christian, Jeanneret, Romain, Witschard, Denise, Baudin, Carole, Bussy, Gaëtan, Carrel, Hélène

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Asperger syndrome and early-onset schizophrenia associated with a novel MECP2 deleterious missense variant von Curie, Aurore, Lesca, Gaëtan, Bussy, Gérald, Manificat, Sabine, Arnaud, Valérie, Gonzalez, Sibylle, Revol, Olivier, Calender, Alain, Gérard, Daniel, des Portes, Vincent

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Empirical antibiotic therapy modalities for Enterobacteriaceae bloodstream infections in older patients and their impact on mortality: a multicentre retrospective study von Roseau-Vincenti, Albane, Forestier, Emmanuel, Lanoix, Jean-Philippe, Ricard, Cécile, Carret, Marie-Christine, Caraux-Paz, Pauline, Paccalin, Marc, Gavazzi, Gaëtan, Roubaud-Baudron, Claire

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Clinical and Neurocognitive Characterization of a Family With a Novel M epsilon D12 Gene Frameshift Mutation von Lesca, Gaetan, Moizard, Marie-Pierre, Bussy, Gerald, Boggio, Dominique, Hu, Hao, Haas, Stefan, Ropers, Hans Hilger, Kalscheuer, Vera M., Des Portes, Vincent, Labalme, Audrey, Sanlaville, Damien, Edery, Patrick, Raynaud, Martine, Lespinasse, James

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Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation von Lesca, Gaetan, Moizard, Marie-Pierre, Bussy, Gerald, Boggio, Dominique, Hu, Hao, Haas, Stefan A., Ropers, Hans-Hilger, Kalscheuer, Vera M., Des Portes, Vincent, Labalme, Audrey, Sanlaville, Damien, Edery, Patrick, Raynaud, Martine, Lespinasse, James

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Childhood apraxia of speech without intellectual deficit in a patient with cri du chat syndrome von Marignier, Stéphanie, Lesca, Gaetan, Marguin, Jessica, Bussy, Gérald, Sanlaville, Damien, des Portes, Vincent

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Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations von Coton, Julie, Labalme, Audrey, Till, Marianne, Bussy, Gerald, Krifi Papoz, Sonia, Lesca, Gaetan, Heron, Delphine, Sanlaville, Damien, Edery, Patrick, Portes, Vincent, Rossi, Massimiliano

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Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations von Coton, Julie, Labalme, Audrey, Till, Marianne, Bussy, Gerald, Krifi Papoz, Sonia, Lesca, Gaetan, Heron, Delphine, Sanlaville, Damien, Edery, Patrick, des Portes, Vincent, Rossi, Massimiliano

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