检索结果 - Christophe Pécheux

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  1. 1
    X Chromosome-Linked Kallmann Syndrome: Clinical Heterogeneity in Three Siblings Carrying an Intragenic Deletion of the<i>KAL-1</i>Gene

    X Chromosome-Linked Kallmann Syndrome: Clinical Heterogeneity in Three Siblings Carrying an Intragenic Deletion of the<i>KAL-1</i>Gene 由 Nathalie Massin, Christophe Pécheux, Corinne Eloit, Jean-Louis Bensimon, Julie Galey, Frédérique Kuttenn, Jean‐Pierre Hardelin, Catherine Dodé, Philippe Touraine

    出版 2003
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  2. 2
    MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications

    MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic... 由 Cécile Cazeneuve, Tamara Sarkisian, Christophe Pécheux, M Dervichian, Brigitte Nédelec, Philippe Reinert, A. Ayvazyan, Jean‐Claude Kouyoumdjian, Hasmik Ajrapetyan, Marc Delpech, Michel Goossens, Catherine Dodé, Gilles Grateau, Serge Amselem

    出版 1999
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  3. 3
    A Naturally Occurring Human Minidysferlin Protein Repairs Sarcolemmal Lesions in a Mouse Model of Dysferlinopathy

    A Naturally Occurring Human Minidysferlin Protein Repairs Sarcolemmal Lesions in a Mouse Model of Dysferlinopathy 由 Martin Krahn, Nicolas Wein, Marc Bartoli, William Lostal, Sébastien Courrier, Nathalie Bourg-Alibert, Karine Nguyen, Christophe Vial, Nathalie Streichenberger, Véronique Labelle, D. Depétris, Christophe Pécheux, France Leturcq, Pierre Cau, Isabelle Richard, Nicolas Lévy

    出版 2010
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  4. 4
    Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF)

    Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF) 由 Alain Bernot, Corinne Da Silva, Jean‐Louis Petit, Corinne Cruaud, Christophe Caloustian, Valerie Castet, Mehdi Ahmed-Arab, Christiane Dross, Madeleine Dupont, D Cattan, Nizar Smaoui, Catherine Dodé, Christophe Pécheux, Brigitte Nédelec, Jean Medaxian, M Rozenbaum, I Rosner, Marc Delpech, Gilles Grateau, Jacques Demaille, Jean Weissenbach, Isabelle Touitou

    出版 1998
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  5. 5
    Prospective high-throughput genome profiling of advanced cancers: results of the PERMED-01 clinical trial

    Prospective high-throughput genome profiling of advanced cancers: results of the PERMED-01 clinical trial 由 François Bertucci, Anthony Gonçalvès, Arnaud Guillé, José Adélaı̈de, Séverine Garnier, Nadine Carbuccia, Emilien Billon, Pascal Finetti, Patrick Sfumato, Audrey Monneur, Christophe Pécheux, M. Khran, Serge Brunelle, Lénaïg Mescam, Jeanne Thomassin‐Piana, Flora Poizat, Emmanuelle Charafe‐Jauffret, Olivıer Turrini, Éric Lambaudie, Magali Provansal, Jean-Marc Extra, Anne Madroszyk, Marine Gilabert, Renaud Sabatier, Cécile Vicier, Émilie Mamessier, Christian Chabannon, Jihane Pakradouni, Patrice Viens, Fabrice André, Gwénaëlle Gravis, Cornel Popovici, Daniel Birnbaum, Max Chaffanet

    出版 2021
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  6. 6
    Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

    Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome 由 Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont, Anne De Paepe, Nathalie Le Dû, Nadia Soussi‐Yanicostas, Roney S. Coimbra, Sedigheh Delmaghani, Sylvie Compain-Nouaille, Françoise Baverel, Christophe Pécheux, Dominique Le Tessier, Corinne Cruaud, Marc Delpech, Frank Speleman, Stefan Vermeulen, Andrea Amalfitano, Y. Bachelot, Philippe Bouchard, Sylvie Cabrol, Jean‐Claude Carel, Henriette Delemarre-van de Waal, B. Goulet-Salmon, Marie‐Laure Kottler, Odile Richard, Franco Sánchez‐Franco, Robert Saura, Jacques Young, Christine Petit, Jean‐Pierre Hardelin

    出版 2003
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