mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic Success
Szymanowski, Marie, Estebanez, Maria Salomon, Padidela, Raja, Han, Bing, Mosinska, Karolina, Stevens, Adam, Damaj, Lena, Pihan-Le Bars, Florence, Lascouts, Emilie, Reynaud, Rachel, Ferreira, Catherine, Bansept, Claire, de Lonlay, Pascale, Saint-Martin, Cécile, Dunne, Mark J, Banerjee, Indraneel, Arnoux, Jean-Baptiste
Published in The journal of clinical endocrinology and metabolism (01.12.2016)
Published in The journal of clinical endocrinology and metabolism (01.12.2016)
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Copy Number Variation and Epilepsy: State of the Art in the Era of High-Throughput Sequencing—A Multicenter Cohort Study
Baer, Sarah, Schalk, Audrey, Miguet, Marguerite, Schaefer, Élise, El Chehadeh, Salima, Ginglinger, Emmanuelle, de Saint Martin, Anne, Abi Wardé, Marie-Thérèse, Laugel, Vincent, de Feraudy, Yvan, Gauer, Lucas, Hirsch, Edouard, Boulay, Clotilde, Bansept, Claire, Bolocan, Anamaria, Kitadinis, Ismini, Gouronc, Aurélie, Gérard, Bénédicte, Piton, Amélie, Scheidecker, Sophie
Published in Pediatric neurology (01.10.2024)
Published in Pediatric neurology (01.10.2024)
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UQCRC2-related mitochondrial complex III deficiency, about 7 patients
Bansept, Claire, Gaignard, Pauline, Lebigot, Elise, Eyer, Didier, Delplancq, Geoffroy, Hoebeke, Célia, Mazodier, Karin, Ledoyen, Anaïs, Rouzier, Cécile, Fragaki, Konstantina, Ait-El-Mkadem Saadi, Samira, Philippe, Christophe, Bruel, Ange-Line, Faivre, Laurence, Feillet, François, Abi Warde, Marie-Thérèse
Published in Mitochondrion (01.01.2023)
Published in Mitochondrion (01.01.2023)
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Multiple molecular diagnoses in the field of intellectual disability and congenital anomalies: 3.5% of all positive cases
Racine, Caroline, Denommé-Pichon, Anne-Sophie, Engel, Camille, Tran Mau-them, Frederic, Bruel, Ange-Line, Vitobello, Antonio, Safraou, Hana, Sorlin, Arthur, Nambot, Sophie, Delanne, Julian, Garde, Aurore, Colin, Estelle, Moutton, Sébastien, Thevenon, Julien, Jean-Marçais, Nolwenn, Willems, Marjolaine, Geneviève, David, Pinson, Lucile, Perrin, Laurence, Laffargue, Fanny, Lacaze, Elodie, Molin, Arnaud, Gerard, Marion, Lambert, Laetitia, Benigni, Charlotte, Patat, Olivier, Bourgeois, Valentin, Poe, Charlotte, Chevarin, Martin, Couturier, Victor, Philippe, Christophe, Duffourd, Yannis, Faivre, Laurence, Thauvin-Robinet, Christel, Verloes, Alain, Goldenberg, Alice, Masurel, Alice, Vincent, Aline, Frances-Guidet, Anne-Marie, Laudier, Béatrice, Demeer, Bénédicte, Funalot, Benoit, Doray, Bérénice, Gilbert-Dussardier, Brigitte, Leheup, Bruno, Poirsier, Céline, Dubucs, Charlotte, Chiaverini, Christine, Coubes, Christine, Francannet, Christine, Colson, Cindy, Bansept, Claire, Wells, Constance, Goizet, Cyril, Mignot, Cyril, Amram, Daniel, Amsallem, Daniel, Lacombe, Didier, Martin-Coignard, Dominique, Schaefer, Elise, Guiliano, Fabienne, Prieur, Fabienne, Petit, Florence, Riccardi, Florence, Meloni, Francesca, Feillet, François, Guyader, Gwenael Le, Journel, Hubert, Coupier, Isabelle, Maystadt, Isabelle, Alessandri, Jean-Luc, Ruaud, Lyse, Jacquemont, Marie-Line, Bonnet-Dupeyron, Marie Noëlle, Lebrun, Marine, Spodenkiewicz, Marta, Renaud, Mathilde, Grelet, Maude, Chassaing, Nicolas, Philip, Nicole, Boute, Odile, Pujol, Pascal, Blanchet, Patricia, Kien, Philippe Khau Van, Parent, Philippe, Vabres, Pierre, Touraine, Renaud, Caumes, Roseline, Sigaudy, Sabine, Whalen, Sandra, Passemard, Sandrine, Grotto, Sarah, Bellanger, Séverine Audebert, Julia, Sophie, Bertrand, Thierry Lavabre, Busa, Tiffany, Layet, Valérie, Bizaoui, Varoona, Trujillo, Yaumara Perdomo, Capri, Yline
Published in Journal of medical genetics (01.01.2024)
Published in Journal of medical genetics (01.01.2024)
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