A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction von Froguel, Philippe, Clément, Karine, Vaisse, Christian, Lahlou, Najiba, Cabrol, Sylvie, Pelloux, Veronique, Cassuto, Dominique, Gourmelen, Micheline, Dina, Christian, Chambaz, Jean, Lacorte, Jean-Marc, Basdevant, Arnaud, Bougnères, Pierre, Lebouc, Yves, Guy-Grand, Bernard

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Cardiovascular findings and management in Turner syndrome: insights from a French cohort von Donadille, Bruno, Rousseau, Alexandra, Zenaty, Delphine, Cabrol, Sylvie, Courtillot, Carine, Samara-Boustani, Dinane, Salenave, Sylvie, Monnier-Cholley, Laurence, Meuleman, Catherine, Jondeau, Guillaume, Iserin, Laurence, Duranteau, Lise, Cabanes, Laure, Bourcigaux, Nathalie, Bonnet, Damien, Bouchard, Philippe, Chanson, Philippe, Polak, Michel, Touraine, Philippe, Lebouc, Yves, Carel, Jean-Claude, Léger, Juliane, Christin-Maitre, Sophie

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Mutations in the Human Leptin and Leptin Receptor Genes as Models of Serum Leptin Receptor Regulation von LAHLOU, Najiba, ISSAD, Tarik, LEBOUC, Yves, CAREL, Jean-Claude, CAMOIN, Luc, ROGER, Marc, GIRARD, Jean

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Growth hormone treatment for childhood short stature and risk of stroke in early adulthood von Linglart, Agnes, Tauber, Maithe, Bougneres, Pierre, Lebouc, Yves, Chatelain, Pierre, Geffner, Mitchell E, Santen, Richard, Kopchick, John

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High risk of adrenal insufficiency after a single articular steroid injection in athletes von DUCLOS, Martine, GUINOT, Michel, COLSY, Marina, MERLE, Francis, BAUDOT, Christophe, BENOIT CORCUFF, Jean, LEBOUC, Yves

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Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vi... von Souberbielle, Jean-Claude, Benhamou, Claude Laurent, Cortet, Bernard, Rousière, Mickael, Roux, Christian, Abitbol, Vered, Annweiler, Cédric, Audran, Maurice, Bacchetta, Justine, Bataille, Pierre, Beauchet, Olivier, Bardet, Rémi, Benachi, Alexandra, Berenbaum, Francis, Blain, Hubert, Borson-Chazot, Françoise, Breuil, Véronique, Briot, Karine, Brunet, Philippe, Carel, Jean-Claude, Caron, Philippe, Chabre, Olivier, Chanson, Philippe, Chapurlat, Roland, Cochat, Pierre, Coutant, Régis, Christin-Maitre, Sophie, Cohen-Solal, Martine, Combe, Christian, Cormier, Catherine, Courbebaisse, Marie, Debrus, Grégory, Delemer, Brigitte, Deschenes, Georges, Duquenne, Marc, Fardellone, Patrice, Fouque, Denis, Friedlander, Gérard, Gauvain, Jean-Bernard, Groussin, Lionel, Guggenbuhl, Pascal, Houillier, Pascal, Hannedouche, Thierry, Jacot, William, Javier, Rose-Marie, Jean, Guillaume, Jeandel, Claude, Joly, Dominique, Kamenicky, Peter, Knebelmann, Bertrand, Lafage-Proust, Marie-Hélène, LeBouc, Yves, Legrand, Erick, Levy-Weil, Florence, Linglart, Agnès, Machet, Laurent, Maheu, Emmanuel, Mallet, Eric, Marcelli, Christian, Marès, Pierre, Mariat, Christophe, Maruani, Gérard, Maugars, Yves, Montagnon, France, Moulin, Bruno, Orcel, Philippe, Partouche, Henri, Personne, Virginie, Pierrot-Deseilligny, Charles, Polak, Michel, Pouteil-Noble, Claire, Prié, Dominique, Raynaud-Simon, Agathe, Rolland, Yves, Sadoul, Jean-Louis, Salle, Bernard, Sault, Corinne, Schott, Anne-Marie, Sermet-Gaudelus, Isabelle, Soubrier, Martin, Tack, Ivan, Thervet, Éric, Tostivint, Isabelle, Touraine, Philippe, Tremollières, Florence, Urena-Torres, Pablo, Viard, Jean-Paul, Wemeau, Jean-Louis, Weryha, Georges, Winer, Norbert, Young, Jacques, Thomas, Thierry

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Growth Hormone Testing for the Diagnosis of Growth Hormone Deficiency in Childhood: A Population Register-Based Study von Carel, Jean-Claude, Tresca, Jean-Pierre, Letrait, Muriel, Chaussain, Jean-Louis, Lebouc, Yves, Job, Jean-Claude, Coste, Joel

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PROVISION OF A MEDICAL RISK ASSESSMENT FOR NONCLASSICAL 21-HYDROXYLASE DEFICIENCY von BACHELOT, Anne, YOUNG, Jacques, LEBOUC, Yves, BACHELOT, Guillaume, LAMAZIERE, Antonin

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Soluble Leptin Receptor in Serum of Subjects With Complete Resistance to Leptin von Lahlou, Najiba, Clement, Karine, Carel, Jean-Claude, Vaisse, Christian, Lotton, Chantal, Le Bihan, Yvette, Basdevant, Arnaud, Lebouc, Yves, Froguel, Philippe, Roger, Marc, Guy-Grand, Bernard

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Characterization of cDNA clones for human glycophorin A: use for gene localization and for analysis of normal of glycophorin-A-deficient (Finnish type) genomic DNA von RAHUEL, C, LONDON, J, D'AURIOL, L, MATTEI, M.-G, TOURNAMILLE, C, SKRZYNIA, C, LEBOUC, Y, GALIBERT, F, CARTRON, J.-P

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Characterization of cDNA clones for human glycophorin A von RAHUEL, Cécile, LONDON, Jacqueline, d'AURIOL, Luc, MATTEI, Marie‐Geneviève, TOURNAMILLE, Christophe, SKRZYNIA, Cécile, LEBOUC, Yves, GALIBERT, Francis, CARTRON, Jean‐Pierre

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Trisomy 16p in a liveborn offspring due to maternal translocation t(16;21)(q11;p11) and review of the literature von Léonard, Claude, Huret, Jean Loup, Imbert, Marie-Claude, Lebouc, Yves, Selva, Jacqueline, Boulley, Anne-Marie

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Cluster analysis identifies long COVID subtypes in Belgian patients von Mfouth Kemajou, Pamela, Besse-Hammer, Tatiana, Lebouc, Claire, Coppieters, Yves

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Thoracic epidural analgesia in intensive care unit patients with acute pancreatitis: the EPIPAN multicenter randomized controlled trial von Jabaudon, Matthieu, Genevrier, Alexandra, Jaber, Samir, Windisch, Olivier, Bulyez, Stéphanie, Laterre, Pierre-François, Escudier, Etienne, Sossou, Achille, Guerci, Philippe, Bertrand, Pierre-Marie, Danin, Pierre-Eric, Bonnassieux, Martin, Bühler, Leo, Heidegger, Claudia Paula, Chabanne, Russell, Godet, Thomas, Roszyk, Laurence, Sapin, Vincent, Futier, Emmanuel, Pereira, Bruno, Constantin, Jean-Michel

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Magnetic structures for contactless temperature sensor von Mavrudieva, Diana, Voyant, Jean-Yves, Kedous-Lebouc, Afef, Yonnet, Jean-Paul

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Structural and functional abnormalities at 11p15 are associated with the malignant phenotype in sporadic adrenocortical tumors : Study on a series of 82 tumors von GICQUEL, C, RAFFIN-SANSON, M.-L, GASTON, V, BERTAGNA, X, PLOUIN, P.-F, SCHLUMBERGER, M, LOUVEL, A, LUTON, J.-P, LE BOUC, Y

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Imprinting mutations in the Beckwith—Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2–H19 domain von Reik, Wolf, Brown, Keith W., Schneid, Helene, Le Bouc, Yves, Bickmore, Wendy, Maher, Eamonn R.

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Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome von Schneid, H, Seurin, D, Vazquez, M P, Gourmelen, M, Cabrol, S, Le Bouc, Y

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Insulin-like growth factors, their binding proteins, and transforming growth factor-beta 1 in oxidant-arrested lung alveolar epithelial cells von CAZALS, V, BANINE MOUHIEDDINE, MAITRE, B, LE BOUC, Y, CHADELAT, K, BRODY, J. S, CLEMENT, A

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Insulin-like growth factors and their binding proteins in pleural fluid von LE BOUC, Y, BELLOCQ, A, PHILIPPE, C, PERIN, L, GARABEDIAN, M, FOUQUERAY, B, ZACHARIAS, C, CADRANEL, J, BAUD, L

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