Rezultati - Feingold, Josué

Identifying modifier genes of monogenic disease: strategies and difficulties od Genin, Emmanuelle, Feingold, Josué, Clerget-Darpoux, Françoise

Polni tekst Polni tekst Polni tekst

Long-term outcome of presymptomatic testing in Huntington disease od Gargiulo, Marcela, Lejeune, Séverine, Tanguy, Marie-Laure, Lahlou-Laforêt, Khadija, Faudet, Anne, Cohen, David, Feingold, Josué, Durr, Alexandra

Polni tekst Polni tekst Polni tekst

Involvement of the Modifier Gene of a Human Mendelian Disorder in a Negative Selection Process od Jéru, Isabelle, Hayrapetyan, Hasmik, Duquesnoy, Philippe, Cochet, Emmanuelle, Serre, Jean-Louis, Feingold, Josué, Grateau, Gilles, Sarkisian, Tamara, Jeanpierre, Marc, Amselem, Serge

Polni tekst Polni tekst Polni tekst

Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France od Rey, Françoise, Berthelon, Monique, Caillaud, Catherine, Lyonnet, Stanislas, Abadie, Véronique, Blandin-Savoja, Félicienne, Feingold, Josué, Saudubray, Jean-Marie, Frézal, Jean, Munnich, Arnold, Rey, Jean

Polni tekst Polni tekst

Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis od 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

Polni tekst Polni tekst Polni tekst

Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients od 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

Polni tekst Polni tekst Polni tekst

Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression od 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

Polni tekst Polni tekst Polni tekst

rs5888 Variant of SCARB1 Gene Is a Possible Susceptibility Factor for Age-Related Macular Degeneration od 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.

Polni tekst Polni tekst Polni tekst

Genetic association study of mitochondrial polymorphisms in neovascular age-related macular degeneration od 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.

Polni tekst Polni tekst

Segregation of mtDNA Throughout Human Embryofetal Development: m.3243A > G as a Model System od 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

Polni tekst Polni tekst Polni tekst

Poor Correlations in the Levels of Pathogenic Mitochondrial DNA Mutations in Polar Bodies versus Oocytes and Blastomeres in Humans od 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

Polni tekst Polni tekst Polni tekst

Anonymous Marker Loci within 400 kb of HLA-A Generate Haplotypes in Linkage Disequilibrium with the Hemochromatosis Gene (HFE) od 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

Polni tekst Polni tekst

Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy od 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

Polni tekst Polni tekst Polni tekst