खोज परिणाम - Feingold, Josué
- प्रदर्शित 1 - 13 परिणाम 13
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Long-term outcome of presymptomatic testing in Huntington disease द्वारा Gargiulo, Marcela, Lejeune, Séverine, Tanguy, Marie-Laure, Lahlou-Laforêt, Khadija, Faudet, Anne, Cohen, David, Feingold, Josué, Durr, Alexandra
प्रकाशित 2009मूलपाठ -
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Involvement of the Modifier Gene of a Human Mendelian Disorder in a Negative Selection Process द्वारा Jéru, Isabelle, Hayrapetyan, Hasmik, Duquesnoy, Philippe, Cochet, Emmanuelle, Serre, Jean-Louis, Feingold, Josué, Grateau, Gilles, Sarkisian, Tamara, Jeanpierre, Marc, Amselem, Serge
प्रकाशित 2009मूलपाठ -
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Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France द्वारा Rey, Françoise, Berthelon, Monique, Caillaud, Catherine, Lyonnet, Stanislas, Abadie, Véronique, Blandin-Savoja, Félicienne, Feingold, Josué, Saudubray, Jean-Marie, Frézal, Jean, Munnich, Arnold, Rey, Jean
प्रकाशित 1988मूलपाठ -
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Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis द्वारा Corvol, Harriet, Nathan, Nadia, Charlier, Celine, Chadelat, Katarina, Le Rouzic, Philippe, Tabary, Olivier, Fauroux, Brigitte, Henrion-Caude, Alexandra, Feingold, Josue, Boelle, Pierre-Yves, Clement, Annick
प्रकाशित 2007मूलपाठ -
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Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients द्वारा Lorenz, Delia, Klebe, Stephan, Stevanin, Giovanni, Thier, Sandra, Nebel, Almut, Feingold, Josué, Frederiksen, Henrik, Denis, Elodie, Christensen, Kaare, Schreiber, Stefan, Brice, Alexis, Deuschl, Günther, Dürr, Alexandra
प्रकाशित 2009मूलपाठ -
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Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression द्वारा Mochel, Fanny, Charles, Perrine, Seguin, François, Barritault, Julie, Coussieu, Christiane, Perin, Laurence, Le Bouc, Yves, Gervais, Christiane, Carcelain, Guislaine, Vassault, Anne, Feingold, Josué, Rabier, Daniel, Durr, Alexandra
प्रकाशित 2007मूलपाठ -
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rs5888 Variant of SCARB1 Gene Is a Possible Susceptibility Factor for Age-Related Macular Degeneration द्वारा Zerbib, Jennyfer, Seddon, Johanna M., Richard, Florence, Reynolds, Robyn, Leveziel, Nicolas, Benlian, Pascale, Borel, Patrick, Feingold, Josué, Munnich, Arnold, Soubrane, Gisèle, Kaplan, Josseline, Rozet, Jean-Michel, Souied, Eric H.
प्रकाशित 2009मूलपाठ -
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Genetic association study of mitochondrial polymorphisms in neovascular age-related macular degeneration द्वारा Tilleul, Julien, Richard, Florence, Puche, Nathalie, Zerbib, Jennyfer, Leveziel, Nicolas, Sahel, Jose Alain, Cohen, Salomon Yves, Korobelnik, Jean-Francois, Feingold, Josue, Munnich, Arnold, Kaplan, Josseline, Rozet, Jean-Michel, Souied, Eric H.
प्रकाशित 2013मूलपाठ -
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Segregation of mtDNA Throughout Human Embryofetal Development: m.3243A > G as a Model System द्वारा Monnot, Sophie, Gigarel, Nadine, Samuels, David C, Burlet, Philippe, Hesters, Laetitia, Frydman, Nelly, Frydman, René, Kerbrat, Violaine, Funalot, Benoit, Martinovic, Jelena, Benachi, Alexandra, Feingold, Josué, Munnich, Arnold, Bonnefont, Jean-Paul, Steffann, Julie
प्रकाशित 2011मूलपाठ -
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Poor Correlations in the Levels of Pathogenic Mitochondrial DNA Mutations in Polar Bodies versus Oocytes and Blastomeres in Humans द्वारा Gigarel, Nadine, Hesters, Laetitia, Samuels, David C., Monnot, Sophie, Burlet, Philippe, Kerbrat, Violaine, Lamazou, Frédéric, Benachi, Alexandra, Frydman, René, Feingold, Josué, Rotig, Agnes, Munnich, Arnold, Bonnefont, Jean-Paul, Frydman, Nelly, Steffann, Julie
प्रकाशित 2011मूलपाठ -
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Anonymous Marker Loci within 400 kb of HLA-A Generate Haplotypes in Linkage Disequilibrium with the Hemochromatosis Gene (HFE) द्वारा Yaouanq, Jacqueline, Perichon, Muriel, Chorney, Michael, Pontarotti, Pierre, Le Treut, André, El Kahloun, Abdel, Mauvieux, Valérie, Blayau, Martine, Jouanolle, Anne Marie, Chauvel, Bruno, Moirand, Romain, Nouel, Olivier, Le Gall, Jean Yves, Feingold, Josué, David, Véronique
प्रकाशित 1994मूलपाठ -
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Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy द्वारा Cartault, François, Munier, Patrick, Benko, Edgar, Desguerre, Isabelle, Hanein, Sylvain, Boddaert, Nathalie, Bandiera, Simonetta, Vellayoudom, Jeanine, Krejbich-Trotot, Pascale, Bintner, Marc, Hoarau, Jean-Jacques, Girard, Muriel, Génin, Emmanuelle, de Lonlay, Pascale, Fourmaintraux, Alain, Naville, Magali, Rodriguez, Diana, Feingold, Josué, Renouil, Michel, Munnich, Arnold, Westhof, Eric, Fähling, Michael, Lyonnet, Stanislas, Henrion-Caude, Alexandra
प्रकाशित 2012मूलपाठ