Výsledky vyhledávání - F. Archambeaud
- Zobrazuji výsledky 1 - 10 z 10
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1
The prognosis of diabetic patients with high ankle-brachial index depends on the coexistence of occlusive peripheral artery disease Autor Victor Aboyans, Philippe Lacroix, Minh-Hoang Tran, Claire Salamagne, S. Galinat, F. Archambeaud, Michael H. Criqui, Marc Laskar
Vydáno 2011Artigo -
2
Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness Autor Véronique Pingault, Virginie Bodereau, Viviane Baral, Séverine Marcos, Yuli Watanabe, Asma Chaoui, Corinne Fouveaut, Chrystel Leroy, O. Vérier‐Mine, Christine Francannet, Delphine Dupin‐Deguine, F. Archambeaud, François-Joseph Kurtz, Jacques Young, Jérôme Bertherat, Sandrine Marlin, Michel Goossens, Jean‐Pierre Hardelin, Catherine Dodé, Nadège Bondurand
Vydáno 2013Artigo -
3
French Endocrine Society Guidance on endocrine side effects of immunotherapy Autor Frédéric Castinetti, F. Albarel, F. Archambeaud, Jérôme Bertherat, Benjamin Bouillet, P. Buffier, Claire Briet, Bertrand Cariou, P. Caron, Olivier Chabre, P. Chanson, Christine Cortet, Christine Do Cao, D. Drui, M Haïssaguerre, S. Hescot, F. Illouz, Emmanuelle Kuhn, N. Lahlou, E. Merlen, Véronique Raverot, Sarra Smati, Bruno Vergès, Françoise Borson‐Chazot
Vydáno 2018Artigo -
4
The Prevalence of<i>CHD7</i>Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients Autor Séverine Marcos, Julie Sarfati, Chrystel Leroy, Corinne Fouveaut, Philippe Parent, Chantal Metz, Sławomir Wołczyński, Marion Gérard, Éric Bieth, F Kurtz, O. Vérier‐Mine, Laurence Perrin, F. Archambeaud, Sylvie Cabrol, Patrice Rodien, Hanne Hove, Trine Prescott, Didier Lacombe, Sophie Christin-Maître, Philippe Touraine, S. Hiéronimus, Didier Dewailly, Jacques Young, Michel Pugeat, Jean‐Pierre Hardelin, Catherine Dodé
Vydáno 2014Artigo -
5
Frequency and Incidence of Carney Complex Manifestations: A Prospective Multicenter Study With a Three-Year Follow-Up Autor Stéphanie Espiard, Marie‐Christine Vantyghem, Guillaume Assié, Catherine Cardot-Bauters, Gérald Raverot, Françoise Brücker-Davis, F Archambeaud-Mouveroux, Hervé Lefèbvre, Marie‐Laure Nunes, Antoine Tabarin, Anne Lienhardt, Olivier Chabre, Muriel Houang, Muriel Bottineau, Sébastian Ströer, Lionel Groussin, Laurence Guignat, Laure Cabanes, A. Feydy, Fidéline Bonnet-Serrano, Marie Odile North, N. Dupin, Sophie Grabar, Denis Duboc, Jérôme Bertherat
Vydáno 2020Artigo -
6
Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real‐life experience from a national reference network Autor Héléna Mosbah, Marie‐Christine Vantyghem, Estelle Nobécourt, Fabrizio Andréelli, F. Archambeaud, Élise Bismuth, Claire Briet, Maryse Cartigny, Benjamin Chevalier, Bruno Donadille, Anne Daguenel, Mathilde Fichet, Jean‐François Gautier, Sonja Janmaat, Isabelle Jéru, Carole Legagneur, Lysiane Leguier, Julie Maître, Elise Mongeois, Christine Poitou, Éric Renard, Yves Reznik, Anne Spiteri, F. Travert, Bruno Vergès, Jamila Zammouri, Corinne Vigouroux, Camille Vatier
Vydáno 2022Artigo -
7
Clinical Characterization of Familial Isolated Pituitary Adenomas Autor Adrian Daly, Marie‐Lise Jaffrain‐Rea, A. Ciccarelli, Hernán Valdés-Socin, V. Rohmer, G. Tamburrano, C. Borson-Chazot, B. Estour, E. Ciccarelli, Thierry Brue, Piero Ferollà, Philippe Émy, Annamaria Colao, Ernesto De Menis, Philippe Lecomte, F. Penfornis, Brigitte Delemer, Jérôme Bertherat, J.-L. Wémeau, Wouter W. de Herder, F. Archambeaud, Achille Stevenaert, Alain Calender, A. Murat, Francesco Cavagnini, Albert Beckers
Vydáno 2006Artigo -
8
Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindreds Autor María A. Tichomirowa, Misu Lee, Anne Barlier, Adrian Daly, Ilaria Marinoni, Marie‐Lise Jaffrain‐Rea, Luciana Ansaneli Naves, Patrice Rodien, V. Rohmer, Fábio R. Faucz, Philippe Caron, Bruno Estour, Pierre Lecomte, Françoise Borson‐Chazot, A. Penfornis, Maria Yaneva, Mirtha Guitelman, E Castermans, Catherine Verhaege, Jean-Louis Wémeau, Antoine Tabarin, Carmen Fajardo, Brigitte Delemer, V. Kerlan, J.L. Sadoul, Christine Cortet Rudelli, F. Archambeaud, Sabine Zacharieva, Marily Theodoropoulou, Thierry Brue, A Enjalbert, Vincent Bours, Natalia S. Pellegata, Albert Beckers
Vydáno 2012Artigo -
9
Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d’étude des Tumeurs Endocrines (GTE) cohort study Autor Julien Thévenon, Abderrahmane Bourredjem, Laurence Bonhomme‐Faivre, Catherine Cardot-Bauters, Alain Calender, Arnaud Murat, Sophie Giraud, Patricia Niccoli, Marie‐Françoise Odou, Françoise Borson‐Chazot, Anne Barlier, Catherine Lombard‐Bohas, Éric Clauser, Antoine Tabarin, Béatrice Parfait, Olivier Chabre, Emilie Castermans, Albert Beckers, Philippe Ruszniewski, Morgane Le Bras, Brigitte Delemer, Philippe Bouchard, Isabelle Guilhem, V. Rohmer, B. Goichot, Philippe Caron, Éric Baudin, Philippe Chanson, Lionel Groussin, Hélène Du Boullay, G. Weryha, Pierre Lecomte, A. Penfornis, H. Bihan, F. Archambeaud, V. Kerlan, F Duron, Jean‐Marc Kuhn, Bruno Vergès, Michel Rodier, M. Renard, Jean‐Louis Sadoul, Christine Binquet, Pierre Goudet
Vydáno 2013Artigo -
10
Aryl Hydrocarbon Receptor-Interacting Protein Gene Mutations in Familial Isolated Pituitary Adenomas: Analysis in 73 Families Autor Adrian F. Daly, Jean-François Vanbellinghen, Sok Kean Khoo, Marie‐Lise Jaffrain‐Rea, Luciana A. Naves, Mirtha A. Guitelman, Arnaud Murat, Philippe Émy, Anne‐Paule Gimenez‐Roqueplo, Guido Tamburrano, Gérald Raverot, Anne Barlier, Wouter W. de Herder, A. Penfornis, E. Ciccarelli, Bruno Estour, Pierre Lecomte, Blandine Gatta, Olivier Chabre, Maria Sabaté, Xavier Bertagna, N. García Basavilbaso, Graciela Stalldecker, Annamaria Colao, Piero Ferollà, Jean-Louis Wémeau, Philippe Caron, Jean-Louis Sadoul, Adriana Oneto, F. Archambeaud, Alain Calender, Olga M. Sinilnikova, Carmen Fajardo, Francesco Cavagnini, Václav Hána, Ángela R. Solano, Dreanina Delettieres, Douglas C. Luccio-Camelo, Armando Basso, V. Rohmer, Thierry Brue, Vincent Bours, Bin Tean Teh, Albert Beckers
Vydáno 2007Artigo
Vyhledávací nástroje:
Související témata
Internal medicine
Medicine
Endocrinology
Biology
Gene
Genetics
Hormone
Carney complex
Disease
Mutation
Oncology
Pediatrics
Acromegaly
Adenoma
Cancer research
Cohort
Context (archaeology)
Coronavirus disease 2019 (COVID-19)
Diabetes mellitus
Endocrine system
Germline
Germline mutation
Growth hormone
Infectious disease (medical specialty)
Kallmann syndrome
MEN1
Multiple endocrine neoplasia
Paleontology
Physics
Pituitary adenoma