Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Gilbert Simonin"'
Autor:
F. Balazard, S. Le Fur, S. Valtat, A. J. Valleron, P. Bougnères, Isis-Diab collaborative group, Dominique Thevenieau, Corinne Fourmy Chatel, Rachel Desailloud, Hélène Bony-Trifunovic, Pierre-Henri Ducluzeau, Régis Coutant, Sophie Caudrelier, Armelle Pambou, Emmanuelle Dubosclard, Florence Joubert, Philippe Jan, Estelle Marcoux, Anne-Marie Bertrand, Brigitte Mignot, Alfred Penformis, Chantal Stuckens, Régis Piquemal, Pascal Barat, Vincent Rigalleau, Chantal Stheneur, Sylviane Fournier, Véronique Kerlan, Chantal Metz, Anne Fargeot-Espaliat, Yves Reznic, Frédérique Olivier, Iva Gueorguieva, Arnaud Monier, Catherine Radet, Vincent Gajdos, Daniel Terral, Christine Vervel, Djamel Bendifallah, Candace Ben Signor, Daniel Dervaux, Abdelkader Benmahammed, Guy-André Loeuille, Françoise Popelard, Agnès Guillou, Pierre-Yves Benhamou, Jamil Khoury, Jean-Pierre Brossier, Joachim Bassil, Sylvaine Clavel, Bernard Le Luyer, Pierre Bougnères, Françoise Labay, Isabelle Guemas, Jacques Weill, Jean-Pierre Cappoen, Sylvie Nadalon, Anne Lienhardt-Roussie, Anne Paoli, Claudie Kerouedan, Edwige Yollin, Marc Nicolino, Gilbert Simonin, Jacques Cohen, Catherine Atlan, Agnès Tamboura, Hervé Dubourg, Marie-Laure Pignol, Philippe Talon, Stéphanie Jellimann, Lucy Chaillous, Sabine Baron, Marie-Noëlle Bortoluzzi, Elisabeth Baechler, Randa Salet, Ariane Zelinsky-Gurung, Fabienne Dallavale, Etienne Larger, Marie Laloi-Michelin, Jean-François Gautier, Bénédicte Guérin, Laure Oilleau, Laetitia Pantalone, Céline Lukas, Isabelle Guilhem, Marc De Kerdanet, Marie-Claire Wielickzo, Mélanie Priou-Guesdon, Odile Richard, François Kurtz, Norbert Laisney, Déborah Ancelle, Guilhem Parlier, Catherine Boniface, Dominique Paris Bockel, Denis Dufillot, Berthe Razafimahefa, Pierre Gourdy, Pierre Lecomte, Myriam Pepin-Donat, Marie-Emmanuelle Combes-Moukhovsky, Brigitte Zymmermann, Marina Raoulx, Anne Gourdin et Catherine Dumont
Publikováno v:
BMC Public Health, Vol 16, Iss 1, Pp 1-10 (2016)
Abstract Background The incidence of childhood type 1 diabetes (T1D) incidence is rising in many countries, supposedly because of changing environmental factors, which are yet largely unknown. The purpose of the study was to unravel environmental mar
Externí odkaz:
https://doaj.org/article/79bbfdce5e9440ecaf010dfed514cf60
Publikováno v:
Annales d'Endocrinologie. 82:279
Les enjeux lies a la transition sont au cœur du suivi des patients en endocrinologie pediatrique puis adulte Objectifs L’objectif principal etait de connaitre le vecu des adolescents ayant eu une consultation de transition en endocrinologie a Mars
Autor:
Noémie Faure-Galon, Valérie Ventura, Elysabeth Baechler-Sadoul, Fabienne Dalla-Vale, Franciane Baucher, Randa Salet, Charlotte Pons, Gilbert Simonin, Rachel Reynaud, Julia Vergier, Florence Joubert, Martine Samper, Murielle De Oliveira, Sophie Epstein, Paola Adiceam
Publikováno v:
PRIMARY CARE DIABETES
PRIMARY CARE DIABETES, 2019, 13 (1), pp.63-70. ⟨10.1016/j.pcd.2018.08.004⟩
PRIMARY CARE DIABETES, 2019, 13 (1), pp.63-70. ⟨10.1016/j.pcd.2018.08.004⟩
Aims: To understand the opinions of children with type 1 diabetes about their everyday use of flash glucose monitoring. (FGM). Methods: Children with type 1 diabetes using the FreeStyle Libre (R) FGM system and/or their parents were surveyed in sever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b5c8fd3aa427e2b4f9350bbce5ebbf4
https://hal.archives-ouvertes.fr/hal-02462180
https://hal.archives-ouvertes.fr/hal-02462180
Autor:
Mariacarolina Salerno, Nancy Mekhail, Monique Jesuran Perelroizen, Rachel Reynaud, Nicolas de Roux, Jean-Claude Carel, Delphine Zenaty, Ibrahima Ba, Juliane Léger, Muriel Houang, Gilbert Simonin, Gianpaolo De Filippo, Dominique Simon, Emmanuel Ecosse, Anne Paulsen
Publikováno v:
European Journal of Endocrinology. 174:1-8
Context and objectiveIdiopathic central precocious puberty (iCPP) is defined as early activation of the hypothalamic–pituitary–gonadal axis in the absence of identifiable central lesions. Mutations of the makorin RING finger 3 (MKRN3) gene are as
Autor:
Jacques Cohen, Isabelle Guilhem, Gilbert Simonin, Françoise Labay, Brigitte Mignot, Chantal Stuckens, Anne-Marie Bertrand, Ariane Zelinsky-Gurung, Dominique Thevenieau, Corinne Fourmy Chatel, Régis Coutant, Vincent Gajdos, S. Le Fur, Marie-Emmanuelle Combes-Moukhovsky, Candace Ben Signor, Djamel Bendifallah, Florence Joubert, Anne Fargeot-Espaliat, Joachim Bassil, Agnès Tamboura, François Kurtz, Norbert Laisney, Agnès Guillou, Lucy Chaillous, Laetitia Pantalone, Sophie Valtat, Marie Laloi-Michelin, Chantal Stheneur, Emmanuelle Dubosclard, Anne Paoli, Véronique Kerlan, Yves Reznic, Sylvaine Clavel, Claudie Kerouedan, Philippe Talon, Armelle Pambou, Iva Gueorguieva, Daniel Dervaux, Hélène Bony-Trifunovic, Régis Piquemal, Pierre Gourdy, Brigitte Zymmermann, Hervé Dubourg, Rachel Desailloud, Stéphanie Jellimann, Pierre-Henri Ducluzeau, Bernard Le Luyer, Guy-André Loeuille, Jamil Khoury, Catherine Atlan, Elisabeth Baechler, Felix Balazard, Berthe Razafimahefa, Pierre Lecomte, Randa Salet, Marina Raoulx, Marie-Laure Pignol, Jean-François Gautier, Christine Vervel, Anne Lienhardt-Roussie, Françoise Popelard, P. Bougnères, Sylviane Fournier, Myriam Pepin-Donat, Mélanie Priou-Guesdon, Marc Nicolino, Sabine Baron, Vincent Rigalleau, Pierre-Yves Benhamou, Edwige Yollin, Marie-Claire Wielickzo, Jacques Weill, Pascal Barat, Déborah Ancelle, Jean-Pierre Brossier, Fabienne Dallavale, Laure Oilleau, Catherine Radet, Sylvie Nadalon, Chantal Metz, Etienne Larger, Céline Lukas, Sophie Caudrelier, Isabelle Guemas, Dominique Paris Bockel, Pierre Bougnères, Arnaud Monier, Estelle Marcoux, Alfred Penformis, Abdelkader Benmahammed, Daniel Terral, Philippe Jan, Marc De Kerdanet, Alain-Jacques Valleron, Catherine Boniface, Denis Dufillot, Frédérique Olivier, Jean-Pierre Cappoen, Anne Gourdin et Catherine Dumont, Guilhem Parlier, Bénédicte Guérin, Marie-Noëlle Bortoluzzi, Odile Richard
Publikováno v:
BMC Public Health
BMC Public Health, BioMed Central, 2016, 16 (1), ⟨10.1186/s12889-016-3690-9⟩
BMC Public Health, 2016, 16 (1), ⟨10.1186/s12889-016-3690-9⟩
BMC Public Health, Vol 16, Iss 1, Pp 1-10 (2016)
BMC Public Health, BioMed Central, 2016, 16 (1), pp.1021. ⟨10.1186/s12889-016-3690-9⟩
BMC Public Health, 2016, 16 (1), pp.1021. ⟨10.1186/s12889-016-3690-9⟩
BMC Public Health, BioMed Central, 2016, 16 (1), ⟨10.1186/s12889-016-3690-9⟩
BMC Public Health, 2016, 16 (1), ⟨10.1186/s12889-016-3690-9⟩
BMC Public Health, Vol 16, Iss 1, Pp 1-10 (2016)
BMC Public Health, BioMed Central, 2016, 16 (1), pp.1021. ⟨10.1186/s12889-016-3690-9⟩
BMC Public Health, 2016, 16 (1), pp.1021. ⟨10.1186/s12889-016-3690-9⟩
BackgroundThe incidence of childhood type 1 diabetes (T1D) incidence is rising in many countries, supposedly because of changing environmental factors, which are yet largely unknown.PurposeTo unravel environmental markers associated with T1D. Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d789a8035ef217a4f1e773151427fc3d
https://hal.univ-brest.fr/hal-02038642
https://hal.univ-brest.fr/hal-02038642
Autor:
Laurent Molines, Aline Cano, Gilbert Simonin, Bernard Vialettes, Véronique Paquis-Flucklinger, René Valéro
Publikováno v:
Diabetes Care. 30:2327-2330
OBJECTIVE—Some previous studies suggested that patients suffering from Wolfram syndrome or DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness) might be relatively preserved from diabetic retinopathy and nephropathy. However
Autor:
Gilbert Simonin, Sophie Vallette-Kasic, Alexandru Saveanu, Anne Barlier, Alain Enjalbert, Paul Valensi, Thierry Brue, Rachel Reynaud, Marie-Pierre Guillet
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2005, 90, pp.4880-4887
Journal of Clinical Endocrinology and Metabolism, 2005, 90, pp.4880-4887
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2005, 90, pp.4880-4887
Journal of Clinical Endocrinology and Metabolism, 2005, 90, pp.4880-4887
Context: PROP1 gene mutations are usually associated with childhood onset GH and TSH deficiencies, whereas gonadotroph deficiency is diagnosed at pubertal age. Objectives: We report a novel PROP1 mutation revealed by familial normosmic hypogonadotrop
Autor:
Alain Enjalbert, M. Chadli-Chaieb, Alexandre Saveanu, Rachel Reynaud, Thierry Brue, Anne Barlier, Gilbert Simonin
Publikováno v:
La Presse Médicale. 33:400-405
Resume L’origine genetique, de plus en plus souvent incriminee Les deficits hypophysaires congenitaux peuvent relever d’une origine genetique alterant le developpement embryonnaire de l’hypophyse. Ce groupe etiologique a connu une grande expans
Autor:
Rachel Reynaud, Anne Paulsen, D. Zenaty, N. De Roux, Gilbert Simonin, Dominique Simon, Jean-Claude Carel, M. Jesuran Perelroizen, Nancy Mekhail, Emmanuel Ecosse, G. De Filippo, Juliane Léger, Muriel Houang, M. Salerno, Ibrahima Ba
Publikováno v:
Annales d'Endocrinologie. 76:315-316
Introduction Des mutations dans le gene MKRN3 ont ete rapportees dans des formes familiales de PPCi. Ce gene est soumis a l’empreinte maternelle et aurait un effet inhibiteur sur la secretion de GnRH. Le but de ce travail a ete d’evaluer la frequ
Autor:
Anne-Marie Guedj, Gilbert Simonin, Rachel Reynaud, Juan Pedro Martinez-Barbera, Philippe Rondard, Anne Guiochon-Mantel, Carine Monnier, Anne Barlier, Jérôme Bouligand, P. Lecomte, Sujatha A. Jayakody, Thierry Brue, Alexandru Saveanu
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, 2012, epub ahead of print. ⟨10.1210/jc.2011-3056⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2012, epub ahead of print. ⟨10.1210/jc.2011-3056⟩
Journal of Clinical Endocrinology and Metabolism, 2012, epub ahead of print. ⟨10.1210/jc.2011-3056⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2012, epub ahead of print. ⟨10.1210/jc.2011-3056⟩
International audience; Context:Pituitary stalk interruption represents a frequent feature of congenital hypopituitarism, but only rare cases have been assigned to a known genetic cause.Objective:Using a candidate gene approach, we tested several gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9eca49a6ec521ab1146923b03ed0e26
https://hal.science/hal-00701550
https://hal.science/hal-00701550