How safe is growth hormone therapy? SAGhE and beyond

por Carel, Jean-Claude
Publicado 2013

Hyperthyroidism in Childhood: Causes, When and How to Treat

por Léger, Juliane, Carel, Jean Claude
Publicado 2013

Central Precocious Puberty – Management and Long-term Outcomes

por Léger, Juliane, Carel, Jean-Claude
Publicado 2015

Association of Pediatric Inpatient Socioeconomic Status With Hospital Efficiency and Financial Balance

por Michel, Morgane, Alberti, Corinne, Carel, Jean-Claude, Chevreul, Karine
Publicado 2019

Increased risk of bone tumors after growth hormone treatment in childhood: A population‐based cohort study in France

por Poidvin, Amélie, Carel, Jean‐Claude, Ecosse, Emmanuel, Levy, Dominique, Michon, Jean, Coste, Joël
Publicado 2018

Growth and Adult Height in Patients with Crohn's Disease Treated with Anti-Tumor Necrosis Factor α Antibodies

por Bamberger, Sarah, Martinez Vinson, Christine, Mohamed, Damir, Viala, Jérôme, Carel, Jean-Claude, Hugot, Jean-Pierre, Simon, Dominique
Publicado 2016

Growth hormone in combination with leuprorelin in pubertal children with idiopathic short stature

por Benabbad, Imane, Rosilio, Myriam, Tauber, Maité, Paris, Emmanuel, Paulsen, Anne, Berggren, Lovisa, Patel, Hiren, Carel, Jean-Claude
Publicado 2018

Can growth hormone treatment improve growth in children with severe growth failure due to anorexia nervosa? A preliminary pilot study

por Léger, Juliane, Fjellestad-Paulsen, Anne, Bargiacchi, Anne, Doyen, Catherine, Ecosse, Emmanuel, Carel, Jean-Claude, Le Heuzey, Marie-France
Publicado 2017

A Simple and Fast Non-Radioactive Bridging Immunoassay for Insulin Autoantibodies

por Kikkas, Ingrid, Mallone, Roberto, Tubiana-Rufi, Nadia, Chevenne, Didier, Carel, Jean Claude, Créminon, Christophe, Volland, Hervé, Boitard, Christian, Morel, Nathalie
Publicado 2013

Association of maternal nutrition with transient neonatal hyperinsulinism

por Louvigne, Mathilde, Rouleau, Stephanie, Caldagues, Emmanuelle, Souto, Isabelle, Montcho, Yanis, Bouvagnet, Audrey Migraine, Baud, Olivier, Carel, Jean Claude, Gascoin, Geraldine, Coutant, Regis
Publicado 2018

Haploinsufficiency of Dmxl2, Encoding a Synaptic Protein, Causes Infertility Associated with a Loss of GnRH Neurons in Mouse

por Tata, Brooke, Huijbregts, Lukas, Jacquier, Sandrine, Csaba, Zsolt, Genin, Emmanuelle, Meyer, Vincent, Leka, Sofia, Dupont, Joelle, Charles, Perrine, Chevenne, Didier, Carel, Jean-Claude, Léger, Juliane, de Roux, Nicolas
Publicado 2014

Recognition of Human Proinsulin Leader Sequence by Class I–Restricted T-Cells in HLA-A*0201 Transgenic Mice and in Human Type 1 Diabetes

por Toma, Andréa, Laïka, Taghrid, Haddouk, Samy, Luce, Sandrine, Briand, Jean-Paul, Camoin, Luc, Connan, Francine, Lambert, Marion, Caillat-Zucman, Sophie, Carel, Jean-Claude, Muller, Sylviane, Choppin, Jeannine, Lemonnier, François, Boitard, Christian
Publicado 2009

HLA-B7–Restricted Islet Epitopes Are Differentially Recognized in Type 1 Diabetic Children and Adults and Form Weak Peptide-HLA Complexes

por Scotto, Matthieu, Afonso, Georgia, Østerbye, Thomas, Larger, Etienne, Luce, Sandrine, Raverdy, Cécile, Novelli, Giulia, Bruno, Graziella, Gonfroy-Leymarie, Céline, Launay, Odile, Lemonnier, François A., Buus, Søren, Carel, Jean-Claude, Boitard, Christian, Mallone, Roberto
Publicado 2012

Glucocorticoid induced adrenal insufficiency in children: Morning cortisol values to avoid LDSST

por Laulhé, Margaux, Dumaine, Cécile, Chevenne, Didier, Leye, Fallou, Faye, Albert, Dozières, Blandine, Strullu, Marion, Viala, Jérome, Hogan, Julien, Houdouin, Véronique, Léger, Juliane, Simon, Dominique, Carel, Jean-Claude, Storey, Caroline, Guilmin-Crépon, Sophie, Martinerie, Laetitia
Publicado 2022

Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseases

por Kallali, Wafa, Messiaen, Claude, Saïdi, Roumaisah, Lessim, Soucounda, Viaud, Magali, Dulon, Jerome, Nedelcu, Mariana, Samara, Dinane, Houang, Muriel, Donadille, Bruno, Courtillot, Carine, de Filippo, GianPaolo, Carel, Jean-Claude, Christin-Maitre, Sophie, Touraine, Philippe, Netchine, Irene, Polak, Michel, Léger, Juliane
Publicado 2021

SUN-040 Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED) Syndrome: Prospective Screening of Asplenism and Pneumonitis in a Cohort of 25 Patients

por Humbert, Linda, Dubucquoi, Sylvain, Kemp, Elizabeth, Saugier-Veber, Pascale, Fabien, Nicole, Isabelle, Raymond Top, Cardot-Bauters, Catherine, Maciejewski Cartigny, Maryse, Delemer, Brigitte, Docao, Christine, Carel, Jean-Claude, Guignat, Laurence, Kerlan, Veronique, Lefevre, Herve, Vanhove, Laura, Sendid, Boualem, Souchon, Pierre-François, Weill, Jacques, Vantyghem, Marie-Christine, Wemeau, Jean-Louis, Proust Lemoine, Emmanuelle
Publicado 2019

Risk of Meningioma in European Patients Treated With Growth Hormone in Childhood: Results From the SAGhE Cohort

por Swerdlow, Anthony J, Cooke, Rosie, Beckers, Dominique, Butler, Gary, Carel, Jean-Claude, Cianfarani, Stefano, Clayton, Peter, Coste, Joël, Deodati, Annalisa, Ecosse, Emmanuel, Hokken-Koelega, Anita C S, Khan, Aysha J, Kiess, Wieland, Kuehni, Claudia E, Flück, Christa E, Pfaffle, Roland, Sävendahl, Lars, Sommer, Grit, Thomas, Muriel, Tidblad, Anders, Tollerfield, Sally, Zandwijken, Gladys R J
Publicado 2018

Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations

por Villanueva, Carine, Jacobson-Dickman, Elka, Xu, Cheng, Manouvrier, Sylvie, Dwyer, Andrew A., Sykiotis, Gerasimos P., Beenken, Andrew, Liu, Yang, Tommiska, Johanna, Hu, Youli, Tiosano, Dov, Gerard, Marion, Leger, Juliane, Drouin-Garraud, Valérie, Lefebvre, Hervé, Polak, Michel, Carel, Jean-Claude, Phan-Hug, Franziska, Hauschild, Michael, Plummer, Lacey, Rey, Jean-Pierre, Raivio, Taneli, Bouloux, Pierre, Sidis, Yisrael, Mohammadi, Moosa, de Roux, Nicolas, Pitteloud, Nelly
Publicado 2014

Mitchell–Riley Syndrome: Improving Clinical Outcomes and Searching for Functional Impact of RFX-6 Mutations

por Passone, Caroline de Gouveia Buff, Vermillac, Gaëlle, Staels, Willem, Besancon, Alix, Kariyawasam, Dulanjalee, Godot, Cécile, Lambe, Cécile, Talbotec, Cécile, Girard, Muriel, Chardot, Christophe, Berteloot, Laureline, Hachem, Taymme, Lapillonne, Alexandre, Poidvin, Amélie, Storey, Caroline, Neve, Mathieu, Stan, Cosmina, Dugelay, Emmanuelle, Fauret-Amsellem, Anne-Laure, Capri, Yline, Cavé, Hélène, Ybarra, Marina, Chandra, Vikash, Scharfmann, Raphaël, Bismuth, Elise, Polak, Michel, Carel, Jean Claude, Pigneur, Bénédicte, Beltrand, Jacques
Publicado 2022

Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46,XY gonadal dysgenesis and 46,XY testicular regression syndrome

por McElreavey, Ken, Jorgensen, Anne, Eozenou, Caroline, Merel, Tiphanie, Bignon-Topalovic, Joelle, Tan, Daisylyn Senna, Houzelstein, Denis, Buonocore, Federica, Warr, Nick, Kay, Raissa G. G., Peycelon, Matthieu, Siffroi, Jean-Pierre, Mazen, Inas, Achermann, John C., Shcherbak, Yuliya, Leger, Juliane, Sallai, Agnes, Carel, Jean-Claude, Martinerie, Laetitia, Le Ru, Romain, Conway, Gerard S., Mignot, Brigitte, Van Maldergem, Lionel, Bertalan, Rita, Globa, Evgenia, Brauner, Raja, Jauch, Ralf, Nef, Serge, Greenfield, Andy, Bashamboo, Anu
Publicado 2019