Multisystem inflammatory syndrome in children rose and fell with the first wave of the COVID‐19 pandemic in France von Carbajal, Ricardo, Lorrot, Mathie, Levy, Yael, Grimprel, Emmanuel, Lecarpentier, Thibault, Heritier, Sebastien, Faivre, Judith, Schnuriger, Aurélie, Parisot, Pauline, Blondiaux, Eléonore, Loschi, Solene, Rivière, Simon, Guilbert, Julia, Romain, Anne‐Sophie, Leger, Pierre‐Louis, Guedj, Romain

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Evaluation of cuffed tracheal tube size predicted using the Khine formula in children von DURACHER, CAROLINE, SCHMAUTZ, EMMANUELLE, MARTINON, CLAIRE, FAIVRE, JUDITH, CARLI, PIERRE, ORLIAGUET, GILLES

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High Mortality Rate for Patients Requiring Intensive Care After Surgical Revision Following Bariatric Surgery von Kermarrec, Nathalie, Marmuse, Jean-Pierre, Faivre, Judith, Lasocki, Sigismond, Mognol, Philippe, Chosidow, Denis, Muller, Claudette, Desmonts, Jean-Marie, Montravers, Philippe

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Intra- and postoperative adverse events in children with nephrotic syndrome requiring surgery under general anesthesia von Greff, Bruno, Faivre, Judith, Carli, Pierre A., Niaudet, Patrick, Orliaguet, Gilles A.

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Place du cathéter central inséré par voie périphérique en pédiatrie en 2017 : indications, techniques et complications von Salvi, Nadège, Faivre-Verroust, Judith

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Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole‐exome sequencing as a first‐line diagnostic test von Thevenon, J., Duffourd, Y., Masurel‐Paulet, A., Lefebvre, M., Feillet, F., El Chehadeh‐Djebbar, S., St‐Onge, J., Steinmetz, A., Huet, F., Chouchane, M., Darmency‐Stamboul, V., Callier, P., Thauvin‐Robinet, C., Faivre, L., Rivière, J.B.

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Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosis von Lefebvre, M., Duffourd, Y., Jouan, T., Poe, C., Jean‐Marçais, N., Verloes, A., St‐Onge, J., Riviere, J.‐B., Petit, F., Pierquin, G., Demeer, B., Callier, P., Thauvin‐Robinet, C., Faivre, L., Thevenon, J.

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[ 68 Ga]Ga‐PentixaFor: Development of a fully automated in hospital production on the Trasis miniAllinOne synthesizer von Costes, Julien, Casasagrande, Kilian, Dubegny, Constance, Castillo, Juan, Kaufman, Jens, Masset, Julien, Vriamont, Charles, Warnier, Corentin, Faivre‐Chauvet, Alain, Delage, Judith Anna

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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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Mosaicism for a KITLG Mutation in Linear and Whorled Nevoid Hypermelanosis von Sorlin, Arthur, Maruani, Annabel, Aubriot-Lorton, Marie-Hélène, Kuentz, Paul, Duffourd, Yannis, Teysseire, Sandra, Carmignac, Virginie, St-Onge, Judith, Chevarin, Martin, Jouan, Thibaud, Thauvin-Robinet, Christel, Thevenon, Julien, Faivre, Laurence, Rivière, Jean-Baptiste, Vabres, Pierre

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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants von Barnes, Daniel R., Rookus, Matti A., Dennis, Joe, Mavaddat, Nasim, Ahmed, Munaza, Aittomäki, Kristiina, Andrulis, Irene L., Arun, Banu K., Barkardottir, Rosa B., Barrowdale, Daniel, Benitez, Javier, Białkowska, Katarzyna, Blok, Marinus J., Bonanni, Bernardo, Bozsik, Aniko, Buys, Saundra S., Caldés, Trinidad, Campbell, Ian, Christensen, Lise Lotte, Colas, Chrystelle, Berthet, Pascaline, Faivre, Laurence, Giraud, Sophie, Lasset, Christine, Mebirouk, Noura, Adlard, Julian, Antoniou, Antonis, Brennan, Paul, Brewer, Carole, Cook, Jackie, Easton, Douglas, Eeles, Ros, Hanson, Helen, Izatt, Louise, Ong, Kai-ren, O’Shaughnessy-Kirwan, Aoife, Daly, Mary B., Davidson, Rosemarie, Ding, Yuan Chun, Dorfling, Cecilia M., Engel, Christoph, Evans, D. Gareth, Friedlander, Michael, Friedman, Eitan, Ganz, Patricia A., Gerdes, Anne-Marie, Giraud, Sophie, Glendon, Gord, Godwin, Andrew K., Gschwantler-Kaulich, Daphne, Hamann, Ute, Hu, Chunling, Hulick, Peter J., Hogervorst, Frans, Koudijs, Marco, Kruse, Torben A., Lazaro, Conxi, Lester, Jenny, Mai, Phuong L., Mari, Véronique, Meijers-Heijboer, Hanne E.J., Meindl, Alfons, Mensenkamp, Arjen R., Montagna, Marco, Mukherjee, Semanti, Mulligan, Anna Marie, Nevanlinna, Heli, Niederacher, Dieter, Olopade, Olufunmilayo I., Ott, Claus-Eric, Papi, Laura, Park, Sue K., Peissel, Bernard, Pfeiler, Georg, Phillips, Kelly-Anne, Prajzendanc, Karolina, Pujana, Miquel Angel, Ramus, Susan J., Rantala, Johanna, Rennert, Gad, Risch, Harvey A., Schuster, Hélène, Senter, Leigha, Side, Lucy E., Slavin, Thomas P., Soucy, Penny, Sutter, Christian, Thull, Darcy L., Toland, Amanda E., Tung, Nadine, van Engelen, Klaartje, van Rensburg, Elizabeth J., Wang-Gohrke, Shan, Wappenschmidt, Barbara, Yang, Xin, Zimbalatti, Dario, Offit, Kenneth, Couch, Fergus J., Schmutzler, Rita K., Antoniou, Antonis C.

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Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis von Nambot, Sophie, Thevenon, Julien, Kuentz, Paul, Duffourd, Yannis, Tisserant, Emilie, Bruel, Ange-Line, Mosca-Boidron, Anne-Laure, Masurel-Paulet, Alice, Lehalle, Daphné, Jean-Marçais, Nolwenn, Lefebvre, Mathilde, Vabres, Pierre, El Chehadeh-Djebbar, Salima, Philippe, Christophe, Tran Mau-Them, Frederic, St-Onge, Judith, Jouan, Thibaud, Chevarin, Martin, Poé, Charlotte, Carmignac, Virginie, Vitobello, Antonio, Callier, Patrick, Rivière, Jean-Baptiste, Faivre, Laurence, Thauvin-Robinet, Christel

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Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing von Kuentz, Paul, St-Onge, Judith, Duffourd, Yannis, Courcet, Jean-Benoît, Carmignac, Virginie, Jouan, Thibaud, Sorlin, Arthur, Abasq-Thomas, Claire, Albuisson, Juliette, Amiel, Jeanne, Amram, Daniel, Arpin, Stéphanie, Attie-Bitach, Tania, Bahi-Buisson, Nadia, Barbarot, Sébastien, Baujat, Geneviève, Bessis, Didier, Boccara, Olivia, Bonnière, Maryse, Boute, Odile, Bursztejn, Anne-Claire, Chiaverini, Christine, Cormier-Daire, Valérie, Coubes, Christine, Delobel, Bruno, Edery, Patrick, Chehadeh, Salima El, Francannet, Christine, Geneviève, David, Goldenberg, Alice, Haye, Damien, Isidor, Bertrand, Jacquemont, Marie-Line, Khau Van Kien, Philippe, Lacombe, Didier, Martin, Ludovic, Martinovic, Jelena, Maruani, Annabel, Mathieu-Dramard, Michèle, Mazereeuw-Hautier, Juliette, Michot, Caroline, Mignot, Cyril, Miquel, Juliette, Morice-Picard, Fanny, Petit, Florence, Phan, Alice, Rossi, Massimiliano, Touraine, Renaud, Verloes, Alain, Vincent, Marie, Vincent-Delorme, Catherine, Whalen, Sandra, Willems, Marjolaine, Marle, Nathalie, Lehalle, Daphné, Thevenon, Julien, Thauvin-Robinet, Christel, Hadj-Rabia, Smaïl, Faivre, Laurence, Vabres, Pierre, Rivière, Jean-Baptiste

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Mosaic‐activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus von Kuentz, P., Fraitag, S., Gonzales, M., Dhombres, F., St‐Onge, J., Duffourd, Y., Joyé, N., Jouannic, J.‐M., Picard, A., Marle, N., Thevenon, J., Thauvin‐Robinet, C., Faivre, L., Rivière, J.‐B., Vabres, P.

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The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation von Thauvin-Robinet, Christel, Lee, Jaclyn S, Lopez, Estelle, Herranz-Pérez, Vicente, Shida, Toshinobu, Franco, Brunella, Jego, Laurence, Ye, Fan, Pasquier, Laurent, Loget, Philippe, Gigot, Nadège, Aral, Bernard, Lopes, Carla A M, St-Onge, Judith, Bruel, Ange-Line, Thevenon, Julien, González-Granero, Susana, Alby, Caroline, Munnich, Arnold, Vekemans, Michel, Huet, Frédéric, Fry, Andrew M, Saunier, Sophie, Rivière, Jean-Baptiste, Attié-Bitach, Tania, Garcia-Verdugo, Jose Manuel, Faivre, Laurence, Mégarbané, André, Nachury, Maxence V

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From bench to bedside: 64Cu/177Lu 1C1m-Fc anti TEM-1: mice-to-human dosimetry extrapolations for future theranostic applications von Gnesin, Silvano, Chouin, Nicolas, Cherel, Michel, Dunn, Steven Mark, Schaefer, Niklaus, Faivre-Chauvet, Alain, Prior, John O., Delage, Judith Anna

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Impact of DOTA Conjugation on Pharmacokinetics and Immunoreactivity of [ 177 Lu]Lu-1C1m-Fc, an Anti TEM-1 Fusion Protein Antibody in a TEM-1 Positive Tumor Mouse Model von Delage, Judith Anna, Faivre-Chauvet, Alain, Barbet, Jacques, Fierle, Julie Katrin, Schaefer, Niklaus, Coukos, George, Viertl, David, Dunn, Steven Mark, Gnesin, Silvano, Prior, John O

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PIK3R1 Mutations Cause Syndromic Insulin Resistance with Lipoatrophy von Thauvin-Robinet, Christel, Auclair, Martine, Duplomb, Laurence, Caron-Debarle, Martine, Avila, Magali, St-Onge, Judith, Le Merrer, Martine, Le Luyer, Bernard, Héron, Delphine, Mathieu-Dramard, Michèle, Bitoun, Pierre, Petit, Jean-Michel, Odent, Sylvie, Amiel, Jeanne, Picot, Damien, Carmignac, Virginie, Thevenon, Julien, Callier, Patrick, Laville, Martine, Reznik, Yves, Fagour, Cédric, Nunes, Marie-Laure, Capeau, Jacqueline, Lascols, Olivier, Huet, Frédéric, Faivre, Laurence, Vigouroux, Corinne, Rivière, Jean-Baptiste

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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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Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome von Vabres, Pierre, Sorlin, Arthur, Kholmanskikh, Stanislav S., Demeer, Bénédicte, St-Onge, Judith, Duffourd, Yannis, Kuentz, Paul, Courcet, Jean-Benoît, Carmignac, Virginie, Garret, Philippine, Bessis, Didier, Boute, Odile, Bron, Alain, Captier, Guillaume, Carmi, Esther, Devauchelle, Bernard, Geneviève, David, Gondry-Jouet, Catherine, Guibaud, Laurent, Lafon, Arnaud, Mathieu-Dramard, Michèle, Thevenon, Julien, Dobyns, William B., Bernard, Geneviève, Polubothu, Satyamaanasa, Faravelli, Francesca, Kinsler, Veronica A., Thauvin, Christel, Faivre, Laurence, Ross, M. Elizabeth, Rivière, Jean-Baptiste

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