Kết quả tìm kiếm - Lamisse Mansour‐Hendili

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  1. 1
    Germline<i>SFTPA1</i>mutation in familial idiopathic interstitial pneumonia and lung cancer

    Germline<i>SFTPA1</i>mutation in familial idiopathic interstitial pneumonia and lung cancer Bằng Nadia Nathan, Violaine Giraud, C. Picard, Hilario Nunès, Florence Dastot‐Le Moal, Bruno Copin, Laurie Galeron, Alice De Ligniville, Nathalie Kuziner, Martine Reynaud‐Gaubert, Dominique Valeyre, Louis‐Jean Couderc, Thierry Chinet, Raphaël Borie, Bruno Crestani, Maud Simansour, Valérie Nau, S. Tissier, Philippe Duquesnoy, Lamisse Mansour‐Hendili, Marie Legendre, Caroline Kannengiesser, Aurore Coulomb‐L'Herminé, Laurent Gouya, Serge Amselem, Annick Clément

    Được phát hành 2016
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    Artigo
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  2. 2
    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 Bằng 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

    Được phát hành 2016
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    Artigo
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  3. 3
    Clinical and Genetic Spectrum of Bartter Syndrome Type 3

    Clinical and Genetic Spectrum of Bartter Syndrome Type 3 Bằng 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

    Được phát hành 2017
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    Artigo
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  4. 4
    Mutation Update of the<i>CLCN5</i>Gene Responsible for Dent Disease 1

    Mutation Update of the<i>CLCN5</i>Gene Responsible for Dent Disease 1 Bằng Lamisse Mansour‐Hendili, Anne Blanchard, Nelly Le Pottier, Isabelle Roncelin, Stéphane Lourdel, Cyrielle Tréard, Wendy González, Ariela Vergara‐Jaque, Gilles Morin, Estelle Colin, Muriel Holder‐Espinasse, Justine Bacchetta, Véronique Baudouin, Stéphane L. Benoit, E. Bérard, Guylhène Bourdat-Michel, Karim Bouchireb, Stéphane Burtey, Mathilde Cailliez, Gérard Cardon, C. Cartery, Gérard Champion, Dominique Chauveau, Pierre Cochat, Karin Dahan, Renaud de la Faille, François-Guillaume Debray, Laurenne Dehoux, Georges Deschênes, Éstelle Desport, Olivier Devuyst, Stella M. Dieguez, Francesco Emma, Michel Fischbach, Denis Fouque, Jacques Fourcade, Arnaud François, Brigitte Gilbert‐Dussardier, Thierry Hannedouche, Pascal Houillier, Hassan Izzedine, Marco Janner, Alexandre Karras, Bertrand Knebelmann, Marie-Pierre Lavocat, Sandrine Lemoine, Valériane Leroy, Chantal Loirat, Marie-Alice Macher, Dominique Martin–Coignard, Denis Morin, Patrick Niaudet, Hubert Nivet, François Nobili, Robert Novo, Laurence Faivre, Claire Rigothier, Gwénaëlle Roussey-Kesler, Rémi Salomon, Andreas Schleich, A.L. Sellier-Leclerc, Kenza Soulami, A. Tiple, Tim Ulinski, Philippe Vanhille, Nicole Van Regemorter, Xavier Jeunemaı̂tre, Rosa Vargas‐Poussou

    Được phát hành 2015
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    Revisão
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