Risultati della ricerca - F. Archambeaud

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  1. 1
    The prognosis of diabetic patients with high ankle-brachial index depends on the coexistence of occlusive peripheral artery disease

    The prognosis of diabetic patients with high ankle-brachial index depends on the coexistence of occlusive peripheral artery disease di Victor Aboyans, Philippe Lacroix, Minh-Hoang Tran, Claire Salamagne, S. Galinat, F. Archambeaud, Michael H. Criqui, Marc Laskar

    Pubblicazione 2011
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  2. 2
    Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness

    Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness di 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

    Pubblicazione 2013
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  3. 3
    French Endocrine Society Guidance on endocrine side effects of immunotherapy

    French Endocrine Society Guidance on endocrine side effects of immunotherapy di 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

    Pubblicazione 2018
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  4. 4
    The Prevalence of<i>CHD7</i>Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients

    The Prevalence of<i>CHD7</i>Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients di 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

    Pubblicazione 2014
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  5. 5
    Frequency and Incidence of Carney Complex Manifestations: A Prospective Multicenter Study With a Three-Year Follow-Up

    Frequency and Incidence of Carney Complex Manifestations: A Prospective Multicenter Study With a Three-Year Follow-Up di 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

    Pubblicazione 2020
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  6. 6
    Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real‐life experience from a national reference network

    Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real‐life experience from a national reference network di 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

    Pubblicazione 2022
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  7. 7
    Clinical Characterization of Familial Isolated Pituitary Adenomas

    Clinical Characterization of Familial Isolated Pituitary Adenomas di 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

    Pubblicazione 2006
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  8. 8
    Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindreds

    Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindreds di 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

    Pubblicazione 2012
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  9. 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

    Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d’étude des Tumeurs Endocrines (GTE) cohort study di 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

    Pubblicazione 2013
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  10. 10
    Aryl Hydrocarbon Receptor-Interacting Protein Gene Mutations in Familial Isolated Pituitary Adenomas: Analysis in 73 Families

    Aryl Hydrocarbon Receptor-Interacting Protein Gene Mutations in Familial Isolated Pituitary Adenomas: Analysis in 73 Families di 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

    Pubblicazione 2007
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