Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)
Mosbah, H, Donadille, B, Vatier, C, Janmaat, S, Atlan, M, Badens, C, Barat, P, Béliard, S, Beltrand, J, Ben Yaou, R, Bismuth, E, Boccara, F, Cariou, B, Chaouat, M, Charriot, G, Christin-Maitre, S, De Kerdanet, M, Delemer, B, Disse, E, Dubois, N, Eymard, B, Fève, B, Lascols, O, Mathurin, P, Nobécourt, E, Poujol-Robert, A, Prevost, G, Richard, P, Sellam, J, Tauveron, I, Treboz, D, Vergès, B, Vermot-Desroches, V, Wahbi, K, Jéru, I, Vantyghem, M C, Vigouroux, C
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Published in Orphanet journal of rare diseases (19.04.2022)
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Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism
de Kerdanet, M, Caron-Debarle, M, Nivot, S, Gaillot, T, Lascols, O, Fremont, B, Bonaure, M, Gie, S, Massart, C, Capeau, J
Published in Diabetes & metabolism (01.09.2015)
Published in Diabetes & metabolism (01.09.2015)
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Growth hormone treatment before the age of 4 years prevents short stature in young girls with Turner syndrome
Linglart, A, Cabrol, S, Berlier, P, Stuckens, C, Wagner, K, de Kerdanet, M, Limoni, C, Carel, J-C, Chaussain, J-L
Published in European journal of endocrinology (01.06.2011)
Published in European journal of endocrinology (01.06.2011)
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Corrigendum to “Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism” [Diabetes Metab. 41 (2015) 331–337]
de Kerdanet, M, Caron-Debarle, M, Nivot, S, Gaillot, T, Lascols, O, Fremont, B, Bonnaure-Mallet, M, Gie, S, Massart, C, Capeau, J
Published in Diabetes & metabolism (01.12.2016)
Published in Diabetes & metabolism (01.12.2016)
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Ketoacidosis at time of diagnosis of type 1 diabetes in children and adolescents: effect of a national prevention campaign
Choleau, C, Maitre, J, Elie, C, Barat, P, Bertrand, A M, de Kerdanet, M, Le Tallec, C, Nicolino, M, Tubiana-Rufi, N, Levy-Marchal, C, Cahané, M, Robert, J-J
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.04.2015)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.04.2015)
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Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy
Van Maldergem, L, Magré, J, Khallouf, T E, Gedde-Dahl, T, Delépine, M, Trygstad, O, Seemanova, E, Stephenson, T, Albott, C S, Bonnici, F, Panz, V R, Medina, J-L, Bogalho, P, Huet, F, Savasta, S, Verloes, A, Robert, J-J, Loret, H, de Kerdanet, M, Tubiana-Rufi, N, Mégarbané, A, Maassen, J, Polak, M, Lacombe, D, Kahn, C R, Silveira, E L, D’Abronzo, F H, Grigorescu, F, Lathrop, M, Capeau, J, O’Rahilly, S
Published in Journal of medical genetics (01.10.2002)
Published in Journal of medical genetics (01.10.2002)
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Metabolic dysfunction in late-puberty adolescent girls with type 1 diabetes: Relationship to physical activity and dietary intakes
Heyman, E, Berthon, P, Youssef, H, Delamarche, A, Briard, D, Gamelin, F.-X, Delamarche, P, de Kerdanet, M
Published in Diabetes & metabolism (01.10.2012)
Published in Diabetes & metabolism (01.10.2012)
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C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients
Alazami, AM, Schneider, SA, Bonneau, D, Pasquier, L, Carecchio, M, Kojovic, M, Steindl, K, De Kerdanet, M, Nezarati, MM, Bhatia, KP, Degos, B, Goh, E, Alkuraya, FS
Published in Clinical genetics (01.12.2010)
Published in Clinical genetics (01.12.2010)
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The control of diabetes and other Non-communicable Diseases is an urgent health priority in Africa: Grenoble declaration
Delisle, L, Besancon, S, Beran, D, Aronica, E, Balcou-Debussche, M, Balde, N, Batal, M, Bernasconi, J, Burgalat, B, Chabre, O, Chancel, P, Comte, E, Coulon, A, Debeaufort, C, Debussche, X, De Kerdanet, M, Delfraissy, J F, Drabo, J, Du-Boullay, H, Duriez, G, Fleury, C, Fontbonne, A, Genay Diliautas, S, Giron, C, Giros, E, Hacquin, D, Mary, C, Micheletti, P, Mohadji, F, Olejas, S, Paquet, C, Quick, I, Raymond, G, Salignon, P, Shojaei, T, Sidibe, A T, Touraine, P, Toure, O, Wackernie, S, Waterlot, C, Weil, O
Published in Médecine et santé tropicales (Montrouge, France) (01.11.2018)
Published in Médecine et santé tropicales (Montrouge, France) (01.11.2018)
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L’acidocétose au diagnostic de diabète de type 1 chez l’enfant et l’adolescent : évolution de la fréquence après une année la campagne d’information
Choleau, C, Maitre, J, Elie, C, Barat, P, Bertrand, A.M, de Kerdanet, M, Le Tallec, C, Levy-Marchal, C, Nicolino, M, Tubiana-Rufi, N, Cahané, M, Robert, J.J
Published in Diabetes & metabolism (26.03.2013)
Published in Diabetes & metabolism (26.03.2013)
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Déficits antéhypophysaires, anomalies morphologiques de l’hypophyse et des bulbes ofactifs dans le syndrome CHARGE
Rodes, M.-L, Gilbert-Dussardier, B, Bellane-chantelot, C, Toutain, A, Odent, S, Colin, E, Rodien, P, Coutant, R, Baron, S, Magontier, N, De Kerdanet, M, Compain, F, Cessans, C, Piguel, X
Published in Annales d'endocrinologie (01.09.2013)
Published in Annales d'endocrinologie (01.09.2013)
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Marqueurs de récidive et morbidité à long terme dans le craniopharyngiome : analyse systématique de 171 patients
Gautier, A, Godbout, A, Grosheny, C, Tejedor, I, Coudert, M.-M, Courtillot, C, Jublanc, C, de Kerdanet, M, Poirier, J.-Y, Riffaud, L, Sainte-Rose, C, Van Effenterre, R, Brassier, G, Bonnet, F, Touraine, P
Published in Annales d'endocrinologie (01.09.2012)
Published in Annales d'endocrinologie (01.09.2012)
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Turner's syndrome with X-isochromosome and Hashimoto's thyroiditis
de Kerdanet, M, Lucas, J, Lemee, F, Lecornu, M
Published in Clinical endocrinology (Oxford) (01.11.1994)
Published in Clinical endocrinology (Oxford) (01.11.1994)
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Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature
Pantel, Jacques, Legendre, Marie, Cabrol, Sylvie, Hilal, Latifa, Hajaji, Yassir, Morisset, Séverine, Nivot, Sylvie, Vie-Luton, Marie-Pierre, Grouselle, Dominique, de Kerdanet, Marc, Kadiri, Abdelkrim, Epelbaum, Jacques, Le Bouc, Yves, Amselem, Serge
Published in The Journal of clinical investigation (01.03.2006)
Published in The Journal of clinical investigation (01.03.2006)
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X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood
Fiot, Elodie, Zénaty, Delphine, Boizeau, Priscilla, Haignere, Jérémie, Dos Santos, Sophie, Léger, Juliane
Published in European journal of endocrinology (01.06.2019)
Published in European journal of endocrinology (01.06.2019)
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Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13
Gedde-Dahl, Tobias, Mégarbané, André, Sobel, Eric, Meier, Muriel, Lathrop, Mark, Capeau, Jacqueline, Papp, Jeanette, Khallouf, Eliane, Van Maldergem, Lionel, Magré, Jocelyne, Delépine, Marc
Published in Nature genetics (01.08.2001)
Published in Nature genetics (01.08.2001)
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Devenir des enfants traités par thyroïdectomie à visée prophylactique dans le cadre d’une NEM2 (étude du GTE)
Morard, I., Oliver, I., Coutant, R., Amouroux, C., Rothenbuhler, A., Marquant, E., Borson-Chazot, F., Castanet, M., Baron, S., De Kerdanet, M., Léger, J., Polak, M., Souchon, P.F., Barat, P., Haissaguerre, M.
Published in Annales d'endocrinologie (01.10.2022)
Published in Annales d'endocrinologie (01.10.2022)
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