檢索結果 - Pascal Barat
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5α-Reductase Type 1 Deficiency or Inhibition Predisposes to Insulin Resistance, Hepatic Steatosis, and Liver Fibrosis in Rodents 由 Dawn E. W. Livingstone, Pascal Barat, Emma M. Di Rollo, Georgina A. Rees, Benjamin A. Weldin, Eva A. Rog‐Zielinska, David P. Macfarlane, Brian R. Walker, Ruth Andrew
出版 2014Artigo -
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Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case 由 Aurore Carré, Gabor Szinnai, Mireille Castanet, Sylvia Sura‐Trueba, Elodie Tron, Isabelle Broutin, Pascal Barat, Cyril Goizet, Didier Lacombe, M.L. Moutard, C. Raybaud, C. Raynaud-Ravni, Serge Romana, H Ythier, Juliane Léger, Mirosław P. Polak
出版 2009Artigo -
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Growth patterns of patients with Noonan syndrome: correlation with age and genotype 由 Catie Cessans, Virginie Ehlinger, Catherine Arnaud, Armelle Yart, Yline Capri, Pascal Barat, B. Cammas, Didier Lacombe, R. Coutant, Albert David, Sabine Baron, Jacques Weill, Bruno Leheup, Marc Nicolino, Jean‐Pierre Salles, Alain Verloès, Maïthé Tauber, Hélène Cavé, Thomas Édouard
出版 2016Artigo -
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SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook 由 Yves Reznik, Pascal Barat, Jérôme Bertherat, Claire Bouvattier, Frédéric Castinetti, Olivier Chabre, Philippe Chanson, Christine Cortet, Brigitte Delemer, B. Goichot, Damien Gruson, Laurence Guignat, Emmanuelle Proust-Lemoine, Marie-Laure Raffin Sanson, Rachel Reynaud, Dinane Samara Boustani, Dominique Simon, Antoine Tabarin, Delphine Zénaty
出版 2018Artigo -
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Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome 由 Antoine Tabarin, Guillaume Assié, Pascal Barat, Fidéline Bonnet-Serrano, Jean François Bonneville, Françoise Borson‐Chazot, Jérôme Bouligand, A. Boulin, Thierry Brue, Philippe Caron, Frédéric Castinetti, Olivier Chabre, Philippe Chanson, J.-B. Corcuff, Christine Cortet, Régis Coutant, Anthony Dohan, D. Drui, Stéphanie Espiard, Delphine Gaye, Solange Grunenwald, Laurence Guignat, Elif Hindié, F. Illouz, Peter Kamenický, Hervé Lefèbvre, Agnès Linglart, Lætitia Martinerie, Marie Odile North, Marie Laure Raffin-Samson, I. Raingeard, Gérald Raverot, Véronique Raverot, Yves Reznik, David Taïeb, Delphine Vezzosi, Jacques Young, Jérôme Bertherat
出版 2022Revisão -
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Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency 由 Julien Cottineau, Molly C. Kottemann, Francis P. Lach, Young‐Hoon Kang, Frédéric Vely, Elissa K. Deenick, Tomi Lazarov, Laure Gineau, Yi Wang, Andrea Farina, Marie Chansel, Lazaro Lorenzo, Christelle Pipéroglou, S. Cindy, Patrick Nitschké, Aziz Belkadi, Yuval Itan, Bertrand Boisson, Fabienne Jabot‐Hanin, Capucine Pïcard, Jacinta Bustamante, Céline Eidenschenk, Soraya Boucherit, Nathalie Aladjidi, Didier Lacombe, Pascal Barat, Waseem Qasim, Jane A. Hurst, Andrew J. Pollard, Holm H. Uhlig, Claire Fieschi, Jean Michon, Vladimir P. Bermudez, Laurent Abel, Jean‐Pierre de Villartay, Frédéric Geissmann, Stuart G. Tangye, Jerard Hurwitz, Éric Vivier, Jean‐Laurent Casanova, Agata Smogorzewska, Emmanuelle Jouanguy
出版 2017Artigo
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