Search Results - Saugier, Jacques

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  1. 1
    Hommage à Joël Barthe

    Hommage à Joël Barthe by Bisserier, Anne, Gouilly, Pascal, Tilly, Henry, Cabillic, Michel, Conil, Pierre, Saugier, Jacques, Pelca, Dominique, Fausser, Claude, Evenou, Dider, Boueiri, Georges, Joud, Philippe, Halimi, Mohamad, Tilly, Henry, Delplanque, Dominique, Garnier, Alain, Zuani, Pierre, Remondiere, Rémi, Schnitter, Claude, Gedda, Michel

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  2. 2
    Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases

    Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases by Adle-Biassette, Homa, Saugier-Veber, Pascale, Fallet-Bianco, Catherine, Delezoide, Anne-Lise, Razavi, Férecheté, Drouot, Nathalie, Bazin, Anne, Beaufrère, Anne-Marie, Bessières, Bettina, Blesson, Sophie, Bucourt, Martine, Carles, Dominique, Devisme, Louise, Dijoud, Frédérique, Fabre, Blandine, Fernandez, Carla, Gaillard, Dominique, Gonzales, Marie, Jossic, Frédérique, Joubert, Madeleine, Laurent, Nicole, Leroy, Brigitte, Loeuillet, Laurence, Loget, Philippe, Marcorelles, Pascale, Martinovic, Jelena, Perez, Marie-José, Satge, Daniel, Sinico, Martine, Tosi, Mario, Benichou, Jacques, Gressens, Pierre, Frebourg, Thierry, Laquerrière, Annie

    Published in Acta neuropathologica
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  3. 3
    SUN-040 Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED) Syndrome: Prospective Screening of Asplenism and Pneumonitis in a Cohort of 25 Patients

    SUN-040 Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED) Syndrome: Prospective Screening of Asplenism and Pneumonitis in a Cohort of 25 Patients by Humbert, Linda, Dubucquoi, Sylvain, Kemp, Elizabeth, Saugier-Veber, Pascale, Fabien, Nicole, Isabelle, Raymond Top, Cardot-Bauters, Catherine, Maciejewski Cartigny, Maryse, Delemer, Brigitte, Docao, Christine, Carel, Jean-Claude, Guignat, Laurence, Kerlan, Veronique, Lefevre, Herve, Vanhove, Laura, Sendid, Boualem, Souchon, Pierre-François, Weill, Jacques, Vantyghem, Marie-Christine, Wemeau, Jean-Louis, Proust Lemoine, Emmanuelle

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  4. 4
    Five years of molecular diagnosis of Fragile X syndrome (1997-2001): A collaborative study reporting 95% of the activity in France

    Five years of molecular diagnosis of Fragile X syndrome (1997-2001): A collaborative study reporting 95% of the activity in France by Biancalana, Valérie, Beldjord, Chérif, Taillandier, Agnès, Szpiro-Tapia, Sylvie, Cusin, Véronica, Gerson, Fabienne, Philippe, Christophe, Mandel, Jean-Louis

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