نتائج البحث - Rachel Reynaud
- يعرض 1 - 17 نتائج من 17
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Limited Value of 18F-F-DOPA PET to Localize Pancreatic Insulin-Secreting Tumors in Adults with Hyperinsulinemic Hypoglycemia حسب Laurent Tessonnier, F. Sébag, C. Ghander, C. De Micco, Rachel Reynaud, F. F. Palazzo, B. Conte‐Devolx, J. F. Henry, O. Mundler, David Taïeb
منشور في 2009Artigo -
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Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms حسب Rachel Reynaud, F. Albarel, Alexandru Saveanu, N. Kaffel, Frédéric Castinetti, Philippe Lecomte, Raja Brauner, G. Simonin, Jean Gaudart, Eva M. Carmona, A Enjalbert, Anne Barlier, Thierry Brue
منشور في 2011Artigo -
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Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections حسب Marie-Hélène Quentien, Brigitte Delemer, Dimitrios T. Papadimitriou, Pierre‐François Souchon, R. Jaussaud, Anne Pagnier, Martine Münzer, Nicolas Jullien, Rachel Reynaud, N. Galon-Faure, A Enjalbert, Anne Barlier, Thierry Brue
منشور في 2011Artigo -
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PROKR2 Variants in Multiple Hypopituitarism with Pituitary Stalk Interruption حسب Rachel Reynaud, Sujatha A. Jayakody, Carine Monnier, Alexandru Saveanu, Jérôme Bouligand, A.M. Guedj, G. Simonin, Pierre Lecomte, Anne Barlier, Philippe Rondard, Juan Pedro Martı́nez-Barberá, Anne Guiochon‐Mantel, Thierry Brue
منشور في 2012Artigo -
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Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty حسب Dominique Simon, Ibrahima Ba, Nancy Mekhail, Emmanuel Écosse, Anne Paulsen, Delphine Zénaty, Muriel Houang, M. Jesuran Perelroizen, Gianpaolo De Filippo, Mariacarolina Salerno, G. Simonin, Rachel Reynaud, Jean‐Claude Carel, Juliane Léger, Nicolás de Roux
منشور في 2015Artigo -
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Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency حسب James Turton, Rachel Reynaud, Ameeta Mehta, John Torpiano, Alexandru Saveanu, Kathryn Woods‐Townsend, Anatoly Tiulpakov, Vera Zdravković, Jill Hamilton, Simon Attard-Montalto, Ray Parascandalo, Cecil Vella, Peter Clayton, Stephen Shalet, John Barton, Thierry Brue, Mehul Dattani
منشور في 2005Artigo -
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mTOR Inhibitors for the Treatment of Severe Congenital Hyperinsulinism: Perspectives on Limited Therapeutic Success حسب Marie Szymanowski, Maria Salomon Estebanez, Raja Padidela, Bing Han, Karolina Mosinska, Adam Stevens, Léna Damaj, Florence Pihan‐Le Bars, Emilie Lascouts, Rachel Reynaud, Catherine Ferreira, Claire Bansept, Pascale de Lonlay, Cécile Saint‐Martin, Mark J. Dunne, Indraneel Banerjee, Jean‐Baptiste Arnoux
منشور في 2016Artigo -
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SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook حسب 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
منشور في 2018Artigo -
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Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort حسب Nicolas Jullien, Alexandru Saveanu, Julia Vergier, E. Marquant, M.-H. Quentien, Frédéric Castinetti, N. Galon-Faure, Raja Brauner, Z. Turki, M. Tauber, Mohamed El Kholy, Agnès Linglart, Patrice Rodien, N.S. Fedala, Ignacio Bergadá, Christine Cortet‐Rudelli, Michel Polak, Marc Nicolino, Chantal Stuckens, Anne Barlier, Thierry Brue, Rachel Reynaud
منشور في 2020Artigo -
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Minor Hypospadias: The “Tip of the Iceberg” of the Partial Androgen Insensitivity Syndrome حسب Nicolas Kalfa, Pascal Philibert, Ralf Werner, Françoise Audran, Anu Bashamboo, H. Lehors, Myriam Haddad, Jean Michel Guys, Rachel Reynaud, P Alessandrini, Kathy Wagner, J.Y. Kurzenne, F. Bastiani, Jean Bréaud, Jean Stéphane Valla, Gérard Morisson Lacombe, Mattéa Orsini, Jean‐Pierre Daurès, Olaf Hiort, Françoise Paris, Kenneth McElreavey, Charles Sultan
منشور في 2013Artigo -
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A big-data approach to producing descriptive anthropometric references: a feasibility and validation study of paediatric growth charts حسب Barbara Heude, Pauline Scherdel, A. Werner, Morgane Le Guern, Nathalie Gelbert, Déborah Walther, Michel Arnould, M. Bellaïche, Bertrand Chevallier, J Cheymol, Emmanuel Jobez, Sylvie Nguyen, Christine Piétrement, Rachel Reynaud, Jean‐François Salaün, Babak Khoshnood, Jennifer Zeitlin, Jean Maccario, Gérard Bréart, Jean-Christophe Thalabard, Marie‐Aline Charles, Jérémie Botton, Bruno Frandji, Martin Chalumeau
منشور في 2019Artigo -
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Genetic Landscape of a Large Cohort of Primary Ovarian Insufficiency: New Genes and Pathways and Implications for Personalized Medicine حسب Abdelkader Heddar, Çağrı Oğur, Sabrina Corrêa da Costa, Inès Braham, Line Billaud-Rist, Necati Findlinki, Claire Bénéteau, Rachel Reynaud, Khaled Mahmoud, Stéphanie Legrand, Maud Marchand, Isabelle Cedrin Durnerin, Adèle Cantaloube, Maëliss Peigné, Marion Bretault, Bénédicte Dagher Hayeck, Sandrine Pérol, Céline Droumaguet, Sabri Cavkaytar, Carole Nicolas Bonne, Hanen Elloumi, Mohamed Khrouf, Charlotte Rougier Le Masle, Mélanie Fradin, Elsa Le Boette, Perrine Luigi, Anne‐Marie Guerrot, Emmanuelle Ginglinger, Amandine Zampa, Anaïs Fauconnier, Nathalie Auger, Françoise Paris, Elise Boucher, Christelle Cabrol, A. Brun, Laura Guyon, Melanie Berard, Axelle Rivière, Marion Gérard, Sylvie Odent, Brigitte Gilbert‐Dussardier, Bertrand Isidor, Juliette Piard, Laëtitia Lambert, S. Hamamah, Anne Marie Guedj, Aude Brac de la Perrière, Bertrand Godeau, H. Fernandez, Marie-Laure Raffin Sanson, Michel Polak, H. Letur, Sylvie Epelboin, Geneviève Plu‐Bureau, Sławomir Wołczyński, S. Hiéronimus, Kristiina Aittomäki, Sophie Catteau-Jonard, Micheline Misrahi
منشور في 2022Artigo -
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Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine حسب Abdelkader Heddar, Çağrı Oğur, Sabrina Corrêa da Costa, Inès Braham, Line Billaud-Rist, Necati Fındıklı, Claire Bénéteau, Rachel Reynaud, Khaled Mahmoud, Stéphanie Legrand, Maud Marchand, Isabelle Cédrin‐Durnerin, Adèle Cantalloube, Maëliss Peigné, Marion Bretault, Benedicte Dagher-Hayeck, Sandrine Pérol, Céline Droumaguet, Sabri Cavkaytar, Carole Nicolas-Bonne, Hanen Elloumi, Mohamed Khrouf, Charlotte Rougier-LeMasle, Mélanie Fradin, Elsa Le Boette, Perrine Luigi, Anne‐Marie Guerrot, Emmanuelle Ginglinger, Amandine Zampa, Anaïs Fauconnier, Nathalie Auger, Françoise Paris, Elise Brischoux‐Boucher, Christelle Cabrol, A. Brun, Laura Guyon, Melanie Berard, Axelle Rivière, Nicolas Gruchy, Sylvie Odent, Brigitte Gilbert‐Dussardier, Bertrand Isidor, Juliette Piard, Laëtitia Lambert, S. Hamamah, Anne Marie Guedj, Aude Brac de la Perrière, H. Fernandez, Marie‐Laure Raffin‐Sanson, Michel Polak, H. Letur, Sylvie Epelboin, Geneviève Plu‐Bureau, Sławomir Wołczyński, S. Hiéronimus, Kristiina Aittomäki, Sophie Catteau-Jonard, Micheline Misrahi
منشور في 2022Artigo -
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Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol) حسب Elodie Fiot, Bertille Alauze, Bruno Donadille, Dinane Samara‐Boustani, Muriel Houang, Gianpaolo De Filippo, Anne Bachelot, Clémence Delcour, Constance Beyler, E. Bois, E. Bourrat, E. Bui Quoc, Nathalie Bourcigaux, Catherine Chaussain, Ariel Cohen, Martine Cohen‐Solal, Sabrina Corrêa da Costa, Claire Dossier, Stéphane Éderhy, Monique Elmaleh, Laurence Iserin, Hélène Lengline, Armelle Poujol‐Robert, Dominique Roulot, Jérôme Viala, F. Albarel, Élise Bismuth, Valérie Bernard, Claire Bouvattier, Aude Brac, Patricia Bretones, Nathalie Chabbert‐Buffet, Philippe Chanson, R. Coutant, Marguerite de Warren, Béatrice Demaret, Lise Duranteau, Florence Eustache, Lydie Gautheret, Georges Gelwane, Claire Gourbesville, M. Grynberg, Karinne Gueniche, Carina Jorgensen, V. Kerlan, Charlotte Lebrun, Christine Lefèvre, F. Lorenzini, Sylvie Manouvrier, Catherine Pienkowski, Rachel Reynaud, Yves Reznik, Jean‐Pierre Siffroi, Anne‐Claude Tabet, Maïthé Tauber, V. Vautier, Igor Tauveron, Sebastien Wambre, Delphine Zénaty, Irène Netchine, Michel Polak, Philippe Touraine, Jean‐Claude Carel, Sophie Christin‐Maître, Juliane Léger
منشور في 2022Artigo
أدوات البحث:
موضوعات ذات صلة
Medicine
Internal medicine
Biology
Genetics
Endocrinology
Gene
Hormone
Pediatrics
Mutation
Hypopituitarism
Context (archaeology)
Phenotype
Anterior pituitary
Bioinformatics
Insulin
Insulin resistance
Missense mutation
Paleontology
Pituitary gland
Pituitary stalk
Cohort
Etiology
Hyperinsulinism
Adrenal crisis
Adrenal insufficiency
Adrenocorticotropic hormone
Allele
Androgen
Androgen insensitivity syndrome
Androgen receptor