Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty
Simon, Dominique, Ba, Ibrahima, Mekhail, Nancy, Ecosse, Emmanuel, Paulsen, Anne, Zenaty, Delphine, Houang, Muriel, Jesuran Perelroizen, Monique, de Filippo, Gian-Paolo, Salerno, Mariacarolina, Simonin, Gilbert, Reynaud, Rachel, Carel, Jean-Claude, Léger, Juliane, de Roux, Nicolas
Published in European journal of endocrinology (01.01.2016)
Published in European journal of endocrinology (01.01.2016)
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Microvascular Diabetes Complications in Wolfram Syndrome (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness [DIDMOAD])
Cano, Aline, Molines, Laurent, Valéro, René, Simonin, Gilbert, Paquis-Flucklinger, Véronique, Vialettes, Bernard
Published in Diabetes care (01.09.2007)
Published in Diabetes care (01.09.2007)
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Evaluation of flash glucose monitoring after long-term use: A pediatric survey
Vergier, Julia, Samper, Martine, Dalla-Vale, Fabienne, Ventura, Valérie, Baucher, Franciane, Joubert, Florence, Pons, Charlotte, De Oliveira, Murielle, Salet, Randa, Faure-Galon, Noémie, Adiceam, Paola, Baechler-Sadoul, Elysabeth, Epstein, Sophie, Simonin, Gilbert, Reynaud, Rachel
Published in Primary care diabetes (01.02.2019)
Published in Primary care diabetes (01.02.2019)
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PROKR2 Variants in Multiple Hypopituitarism with Pituitary Stalk Interruption
Reynaud, Rachel, Jayakody, Sujatha A, Monnier, Carine, Saveanu, Alexandru, Bouligand, Jérome, Guedj, Anne-Marie, Simonin, Gilbert, Lecomte, Pierre, Barlier, Anne, Rondard, Philippe, Martinez-Barbera, Juan Pedro, Guiochon-Mantel, Anne, Brue, Thierry
Published in The journal of clinical endocrinology and metabolism (01.06.2012)
Published in The journal of clinical endocrinology and metabolism (01.06.2012)
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Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case-control study
Balazard, F, Le Fur, S, Valtat, S, Valleron, A J, Bougnères, P, Thevenieau, Dominique, Chatel, Corinne Fourmy, Desailloud, Rachel, Bony-Trifunovic, Hélène, Ducluzeau, Pierre-Henri, Coutant, Régis, Caudrelier, Sophie, Pambou, Armelle, Dubosclard, Emmanuelle, Joubert, Florence, Jan, Philippe, Marcoux, Estelle, Bertrand, Anne-Marie, Mignot, Brigitte, Penformis, Alfred, Stuckens, Chantal, Piquemal, Régis, Barat, Pascal, Rigalleau, Vincent, Stheneur, Chantal, Fournier, Sylviane, Kerlan, Véronique, Metz, Chantal, Fargeot-Espaliat, Anne, Reznic, Yves, Olivier, Frédérique, Gueorguieva, Iva, Monier, Arnaud, Radet, Catherine, Gajdos, Vincent, Terral, Daniel, Vervel, Christine, Bendifallah, Djamel, Signor, Candace Ben, Dervaux, Daniel, Benmahammed, Abdelkader, Loeuille, Guy-André, Popelard, Françoise, Guillou, Agnès, Benhamou, Pierre-Yves, Khoury, Jamil, Brossier, Jean-Pierre, Bassil, Joachim, Clavel, Sylvaine, Le Luyer, Bernard, Bougnères, Pierre, Labay, Françoise, Guemas, Isabelle, Weill, Jacques, Cappoen, Jean-Pierre, Nadalon, Sylvie, Lienhardt-Roussie, Anne, Paoli, Anne, Kerouedan, Claudie, Yollin, Edwige, Nicolino, Marc, Simonin, Gilbert, Cohen, Jacques, Atlan, Catherine, Tamboura, Agnès, Dubourg, Hervé, Pignol, Marie-Laure, Talon, Philippe, Jellimann, Stéphanie, Chaillous, Lucy, Baron, Sabine, Bortoluzzi, Marie-Noëlle, Baechler, Elisabeth, Salet, Randa, Zelinsky-Gurung, Ariane, Dallavale, Fabienne, Larger, Etienne, Laloi-Michelin, Marie, Gautier, Jean-François, Guérin, Bénédicte, Oilleau, Laure, Pantalone, Laetitia, Lukas, Céline, Guilhem, Isabelle, De Kerdanet, Marc, Wielickzo, Marie-Claire, Priou-Guesdon, Mélanie, Richard, Odile, Kurtz, François, Laisney, Norbert, Ancelle, Déborah, Parlier, Guilhem, Boniface, Catherine, Bockel, Dominique Paris, Dufillot, Denis, Razafimahefa, Berthe, Gourdy, Pierre, Lecomte, Pierre, Pepin-Donat, Myriam, Combes-Moukhovsky, Marie-Emmanuelle
Published in BMC public health (29.09.2016)
Published in BMC public health (29.09.2016)
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An Uncommon Phenotype with Familial Central Hypogonadism Caused by a Novel PROP1 Gene Mutant Truncated in the Transactivation Domain
Reynaud, Rachel, Barlier, Anne, Vallette-Kasic, Sophie, Saveanu, Alexandru, Guillet, Marie-Pierre, Simonin, Gilbert, Enjalbert, Alain, Valensi, Paul, Brue, Thierry
Published in The journal of clinical endocrinology and metabolism (01.08.2005)
Published in The journal of clinical endocrinology and metabolism (01.08.2005)
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Microvascular Diabetes Complications in Wolfram Syndrome (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness [DIDMOAD]): An age- and duration-matched comparison with common type 1 diabetes
Cano, Aline, Molines, Laurent, Valéro, René, Simonin, Gilbert, Paquis-Flucklinger, Véronique, Vialettes, Bernard
Published in Diabetes care (01.09.2007)
Published in Diabetes care (01.09.2007)
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Journal Article
Hypopituitarisme congénital
Reynaud, Rachel, Barlier, Anne, Chadli-Chaieb, Molka, Saveanu, Alexandre, Simonin, Gilbert, Enjalbert, Alain, Brue, Thierry
Published in La Presse médicale (1983) (01.03.2004)
Published in La Presse médicale (1983) (01.03.2004)
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Macroprolactinemia: A Cause of Hyperprolactinemia in Childhood
Fabre-Brue, C., Roth, E., Simonin, G., Palix, C., Martin, P.-M., Brue, T.
Published in Journal of Pediatric Endocrinology and Metabolism (1997)
Published in Journal of Pediatric Endocrinology and Metabolism (1997)
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