Risultati della ricerca - Christophe Simian

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  1. 1
    Mosaicism in<i>HIF2A</i>-Related Polycythemia-Paraganglioma Syndrome

    Mosaicism in<i>HIF2A</i>-Related Polycythemia-Paraganglioma Syndrome di Alexandre Buffet, Sarra Smati, L Mansuy, Mélanie Menara, M. Lebras, Marie‐Françoise Heymann, Christophe Simian, Judith Favier, Arnaud Murat, Bertrand Cariou, Anne‐Paule Gimenez‐Roqueplo

    Pubblicazione 2013
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  2. 2
    The Functional c.-2G&gt;C Variant of the Mineralocorticoid Receptor Modulates Blood Pressure, Renin, and Aldosterone Levels

    The Functional c.-2G&gt;C Variant of the Mineralocorticoid Receptor Modulates Blood Pressure, Renin, and Aldosterone Levels di Nienke van Leeuwen, Massimiliano Caprio, Carolina Blaya, Frédéric Fumeron, Paola Sartorato, Vanessa Ronconi, Gilberta Giacchetti, Franco Mantero, Fábio L. Fernandes‐Rosa, Christophe Simian, S. Peyrard, Frans G. Zitman, Brenda W.J.H. Penninx, E. R. de Kloet, Michel Azizi, Xavier Jeunemaı̂tre, Roel H. DeRijk, Maria‐Christina Zennaro

    Pubblicazione 2010
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  3. 3
    Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas

    Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas di Luis Jaime Castro‐Vega, Alexandre Buffet, Aguirre A. de Cubas, Alberto Cascón, Mélanie Menara, Emmanuel Khalifa, Laurence Amar, Sharona Azriel, Isabelle Bourdeau, Olivier Chabre, María Currás-Freixes, V. Franco‐Vidal, Marine Guillaud-Bataille, Christophe Simian, Aurélie Morin, Rocío Letón, Álvaro Gómez-Graña, Patrick J. Pollard, Pierre Rustin, Mercedes Robledo, Judith Favier, Anne‐Paule Gimenez‐Roqueplo

    Pubblicazione 2013
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  4. 4
    Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences

    Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences di Rosa Vargas‐Poussou, Lamisse Mansour‐Hendili, Stéphanie Baron, Jean‐Philippe Bertocchio, C. Travers, Christophe Simian, Cyrielle Tréard, Véronique Baudouin, Sonia Beltran, Françoise Broux, Odile Camard, Sylvie Cloarec, Catherine Cormier, Xavier Debussche, Emmanuelle Dubosclard, Celine Eid, Jean‐Philippe Haymann, Soto Romuald Kiando, Jean‐Marc Kuhn, Guy Lefort, Agnès Linglart, Bernadette Lucas-Pouliquen, Marie‐Alice Macher, Gérard Maruani, Sophie Ouzounian, Michel Polak, E Requeda, Dominique Robier, Caroline Silve, Jean‐Claude Souberbielle, Ivan Tack, Delphine Vezzosi, Xavier Jeunemaı̂tre, Pascal Houillier

    Pubblicazione 2016
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  5. 5
    Clinical and Genetic Spectrum of Bartter Syndrome Type 3

    Clinical and Genetic Spectrum of Bartter Syndrome Type 3 di Elsa Seys, Olga Andrini, Mathilde Keck, Lamisse Mansour‐Hendili, Pierre‐Yves Courand, Christophe Simian, Georges Deschênes, Thérèsa Kwon, Aurélia Bertholet‐Thomas, Guillaume Bobrie, Jean Sébastien Borde, Guylhène Bourdat-Michel, Stéphane Decramer, Mathilde Cailliez, Pauline Krug, P Cozette, Jean‐Daniel Delbet, Laurence Dubourg, Dominique Chaveau, Marc Fila, Noémie Jourde‐Chiche, Bertrand Knebelmann, Marie‐Pierre Lavocat, Sandrine Lemoine, D. Djeddi, Brigitte Llanas, Férielle Louillet, Élodie Merieau, Maria Mileva, Luísa Mota‐Vieira, Christiane Mousson, François Nobili, Robert Novo, Gwénaëlle Roussey-Kesler, Isabelle Vrillon, Stephen B. Walsh, Jacques Teulon, Anne Blanchard, Rosa Vargas‐Poussou

    Pubblicazione 2017
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