50. Brain Abnormalities in Children With Early-Onset Anorexia by Moreau, Clara, Tran, Lydie, Ayrolles, Anael, Bonicel, Robin, Bergeret, Pierre, Traut, Nicolas, Stordeur, Coline, Thompson, Paul M., Bourgeron, Thomas, Delorme, Richard

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Wireline Logging on CD by Tran, Lydie

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Wireline Logging on CD: by Sylvain Boyer. Edition Technip, Paris, 1999, FF1,200 by Tran, Lydie

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Exceptional Bluetongue virus (BTV) and Epizootic hemorrhagic disease virus (EHDV) circulation in France in 2023 by Gondard, Mathilde, Postic, Lydie, Garin, Emmanuel, Turpaud, Mathilde, Vorimore, Fabien, Ngwa-Mbot, David, Tran, Mai-Lan, Hoffmann, Bernd, Warembourg, Charlotte, Savini, Giovanni, Lorusso, Alessio, Marcacci, Maurilia, Felten, Arnaud, Roux, Aurélie Le, Blanchard, Yannick, Zientara, Stephan, Vitour, Damien, Sailleau, Corinne, Bréard, Emmanuel

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Detection, Characterization and Sequencing of BTV Serotypes Circulating in Cuba in 2022 by Acevedo, Ana María, Postic, Lydie, Curiel, Maray, Gondard, Mathilde, Bréard, Emmanuel, Zientara, Stéphan, Vorimore, Fabien, Tran, Mai-Lan, Turpaud, Mathilde, Savini, Giovanni, Lorusso, Alessio, Marcacci, Maurilia, Vitour, Damien, Dujardin, Pascal, Perera, Carmen Laura, Díaz, Cristian, Obret, Yalainne, Sailleau, Corinne

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Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders by Barbosa, Sónia, Greville-Heygate, Stephanie, Bonnet, Maxime, Godwin, Annie, Fagotto-Kaufmann, Christine, Kajava, Andrey V., Laouteouet, Damien, Mawby, Rebecca, Wai, Htoo Aung, Dingemans, Alexander J.M., Hehir-Kwa, Jayne, Willems, Marjorlaine, Capri, Yline, Mehta, Sarju G., Cox, Helen, Goudie, David, Vansenne, Fleur, Turnpenny, Peter, Vincent, Marie, Cogné, Benjamin, Lesca, Gaëtan, Hertecant, Jozef, Rodriguez, Diana, Keren, Boris, Burglen, Lydie, Gérard, Marion, Putoux, Audrey, Cantagrel, Vincent, Siquier-Pernet, Karine, Rio, Marlene, Banka, Siddharth, Sarkar, Ajoy, Steeves, Marcie, Parker, Michael, Clement, Emma, Moutton, Sébastien, Tran Mau-Them, Frédéric, Piton, Amélie, de Vries, Bert B.A., Guille, Matthew, Debant, Anne, Schmidt, Susanne, Baralle, Diana

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Molecular characterization and mapping of glucose-6-phosphate dehydrogenase (G6PD) mutations in the Greater Mekong Subregion by Bancone, Germana, Menard, Didier, Khim, Nimol, Kim, Saorin, Canier, Lydie, Nguong, Chea, Phommasone, Koukeo, Mayxay, Mayfong, Dittrich, Sabine, Vongsouvath, Malavanh, Fievet, Nadine, Le Hesran, Jean-Yves, Briand, Valerie, Keomany, Sommay, Newton, Paul N, Gorsawun, Gornpan, Tardy, Kaelan, Chu, Cindy S, Rattanapalroj, Orpreeya, Dong, Le Thanh, Quang, Huynh Hong, Tam-Uyen, Nguyen, Thuy-Nhien, Nguyen, Hien, Tran Tinh, Kalnoky, Michael, Nosten, Francois

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Mosaic vaccine-induced antibody-dependent cellular phagocytosis associated with delayed HIV-1 viral load rebound post treatment interruption by Mdluli, Thembi, Slike, Bonnie M., Curtis, Daniel J., Shubin, Zhanna, Tran, Ursula, Li, Yifan, Dussupt, Vincent, Mendez-Rivera, Letzibeth, Pinyakorn, Suteeraporn, Stieh, Daniel J., Tomaka, Frank L., Schuitemaker, Hanneke, Pau, Maria G., Colby, Donn J., Kroon, Eugène, Sacdalan, Carlo, de Souza, Mark, Phanupak, Nittaya, Hsu, Denise C., Ananworanich, Jintanat, Ake, Julie A., Trautmann, Lydie, Vasan, Sandhya, Robb, Merlin L., Krebs, Shelly J., Paquin-Proulx, Dominic, Rolland, Morgane

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Phenotypic spectrum of the recurrent TRPM3 p.(Val837Met) substitution in seven individuals with global developmental delay and hypotonia by Lines, Matthew A., Goldenberg, Paula, Wong, Ashley, Srivastava, Siddharth, Bayat, Allan, Hove, Hanne, Karstensen, Helena Gásdal, Anyane‐Yeboa, Kwame, Liao, Jun, Jiang, Nan, May, Alison, Guzman, Edwin, Morleo, Manuela, D'Arrigo, Stefano, Ciaccio, Claudia, Pantaleoni, Chiara, Castello, Raffaele, McKee, Shane, Ong, Jinfon, Zibdeh‐Lough, Hana, Tran‐Mau‐Them, Frederic, Gerasimenko, Anna, Heron, Delphine, Keren, Boris, Margot, Henri, Sainte Agathe, Jean‐Madeleine, Burglen, Lydie, Voets, Thomas, Vriens, Joris, Innes, A. Micheil, Dyment, David A.

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Impact of rotavirus vaccination on hospitalizations for rotavirus diarrhea: The IVANHOE study by Gagneur, Arnaud, Nowak, Emmanuel, Lemaitre, Thomas, Segura, Jean-Francois, Delaperrière, Nadège, Abalea, Lydie, Poulhazan, Elise, Jossens, Anne, Auzanneau, Lucie, Tran, Adissa, Payan, Christopher, Jay, Nadine, de Parscau, Loic, Oger, Emmanuel

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Correction to ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder by Carapito, Raphaël, Ivanova, Ekaterina, Morlon, Aurore, Meng, Linyan, Molitor, Anne, Erdmann, Eva, Kieffer, Bruno, Pichot, Angélique, Naegely, Lydie, Kolmer, Aline, Paul, Nicodème, Hanauer, Antoine, Tran Mau-Them, Frédéric, Jean-Marçais, Nolwenn, Hiatt, Susan, Cooper, Gregory, Tvrdik, Tatiana, Muir, Alison, Dimartino, Clémantine, Chopra, Maya, Amiel, Jeanne, Gordon, Christopher, Dutreux, Fabien, Garde, Aurore, Thauvin-Robinet, Christel, Wang, Xia, Leduc, Magalie, Phillips, Meredith, Crawford, Heather, Kukolich, Mary, Hunt, David, Harrison, Victoria, Kharbanda, Mira, Smigiel, Robert, Gold, Nina, Hung, Christina, Viskochil, David, Dugan, Sarah, Bayrak-Toydemir, Pinar, Joly-Helas, Géraldine, Guerrot, Anne-Marie, Schluth-Bolard, Caroline, Rio, Marlène, Wentzensen, Ingrid M., Mcwalter, Kirsty, Schnur, Rhonda, Lewis, Andrea, Lalani, Seema, Mensah-Bonsu, Noël, Céraline, Jocelyn, Sun, Zijie, Ploski, Rafal, Bacino, Carlos, Mefford, Heather, Faivre, Laurence, Bodamer, Olaf, Chelly, Jamel, Isidor, Bertrand, Bahram, Seiamak

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A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis by Olson, Heather E., Jean-Marçais, Nolwenn, Yang, Edward, Heron, Delphine, Tatton-Brown, Katrina, van der Zwaag, Paul A., Bijlsma, Emilia K., Krock, Bryan L., Backer, E., Kamsteeg, Erik-Jan, Sinnema, Margje, Reijnders, Margot R.F., Bearden, David, Begtrup, Amber, Telegrafi, Aida, Lunsing, Roelineke J., Burglen, Lydie, Lesca, Gaetan, Cho, Megan T., Smith, Lacey A., Sheidley, Beth R., Moufawad El Achkar, Christelle, Pearl, Phillip L., Poduri, Annapurna, Skraban, Cara M., Tarpinian, Jennifer, Nesbitt, Addie I., Fransen van de Putte, Dietje E., Ruivenkamp, Claudia A.L., Rump, Patrick, Chatron, Nicolas, Sabatier, Isabelle, De Bellescize, Julitta, Guibaud, Laurent, Sweetser, David A., Waxler, Jessica L., Wierenga, Klaas J., Donadieu, Jean, Narayanan, Vinodh, Ramsey, Keri M., Nava, Caroline, Rivière, Jean-Baptiste, Vitobello, Antonio, Tran Mau-Them, Frédéric, Philippe, Christophe, Bruel, Ange-Line, Duffourd, Yannis, Thomas, Laurel, Lelieveld, Stefan H., Schuurs-Hoeijmakers, Janneke, Brunner, Han G., Keren, Boris, Thevenon, Julien, Faivre, Laurence, Thomas, Gary, Thauvin-Robinet, Christel

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A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis by Olson, Heather E., Jean-Marçais, Nolwenn, Yang, Edward, Heron, Delphine, Tatton-Brown, Katrina, van der Zwaag, Paul A., Bijlsma, Emilia K., Krock, Bryan L., Backer, E., Kamsteeg, Erik-Jan, Sinnema, Margje, Reijnders, Margot R.F., Bearden, David, Begtrup, Amber, Telegrafi, Aida, Lunsing, Roelineke J., Burglen, Lydie, Lesca, Gaetan, Cho, Megan T., Smith, Lacey A., Sheidley, Beth R., El Achkar, Christelle Moufawad, Pearl, Phillip L., Poduri, Annapurna, Skraban, Cara M., Tarpinian, Jennifer, Nesbitt, Addie I., Fransen van de Putte, Dietje E., Ruivenkamp, Claudia A.L., Rump, Patrick, Chatron, Nicolas, Sabatier, Isabelle, De Bellescize, Julitta, Guibaud, Laurent, Sweetser, David A., Waxler, Jessica L., Wierenga, Klaas J., Donadieu, Jean, Narayanan, Vinodh, Ramsey, Keri M., Nava, Caroline, Rivière, Jean-Baptiste, Vitobello, Antonio, Mau-Them, Frédéric Tran, Philippe, Christophe, Bruel, Ange-Line, Duffourd, Yannis, Thomas, Laurel, Lelieveld, Stefan H., Schuurs-Hoeijmakers, Janneke, Brunner, Han G., Keren, Boris, Thevenon, Julien, Faivre, Laurence, Thomas, Gary, Thauvin-Robinet, Christel

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