Søgeresultater - Rémy Couderc
- Showing 1 - 12 results of 12
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Early-Onset Atopic Dermatitis in Children: Which Are the Phenotypes at Risk of Asthma? Results from the ORCA Cohort af Flore Amat, Philippe Pierre, E. Bourrat, A. Nemni, Rémy Couderc, Emmanuelle Boutmy, F. Sahraoui, Isabelle Pansé, M. Bagot, S. Fouéré, J. Just
Udgivet 2015Artigo -
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A new allergen family involved in pollen food-associated syndrome: Snakin/gibberellin-regulated proteins af Hélène Sénéchal, Jiří Šantrůček, Magdalena Melčová, Petr Svoboda, J. Zídková, D. Charpin, L. Guilloux, Youcef Shahali, M.A. Selva, Rémy Couderc, Tomoyasu Aizawa, Pascal Poncet
Udgivet 2017Carta -
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Use of a Reference Material Proposed by the International Federation of Clinical Chemistry and Laboratory Medicine to Evaluate Analytical Methods for the Determination of Plasma Li... af Santica M. Marcovina, John J. Albers, Angelo M. Scanu, Hal Kennedy, Federico Giaculli, Kåre Berg, Rémy Couderc, Francesco Dati, Nader Rifai, Ikunosuke Sakurabayashi, Jillian R. Tate, Armin Steinmetz
Udgivet 2000Artigo -
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Heterogeneity of lung disease associated with NK2 homeobox 1 mutations af Elodie Nattes, Stéphanie Lejeune, A. Carsin, Raphaël Borie, Isabelle Gibertini, Juan E. Balinotti, Nadia Nathan, S. Marchand‐Adam, C. Thumerelle, Brigitte Fauroux, E. Bosdure, Véronique Houdouin, Céline Delestrain, Malek Louha, Rémy Couderc, Alix de Becdelièvre, Pascale Fanen, Benoît Funalot, B. Crestani, A. Deschildre, J.‐C. Dubus, Ralph Epaud
Udgivet 2017Artigo -
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Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip af M. Lévêque, Sandrine Marlin, Laurence Jonard, Vincent Procaccio, Pascal Reynier, Patrizia Amati‐Bonneau, Sylvain Baulande, Denis Pierron, Didier Lacombe, F Duriez, Christine Francannet, T. Mom, Hubert Journel, Hélène Catros, Valérie Drouin‐Garraud, Marie-Françoise Obstoy, Hélène Dollfus, Marie‐Madeleine Eliot, Laurence Faivre, C. Duvillard, Rémy Couderc, Éréa-Noël Garabédian, Christine Petit, Delphine Feldmann, Françoise Denoyelle
Udgivet 2007Artigo -
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SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations af Sébastien Albert, Hélène Blons, Laurence Jonard, Delphine Feldmann, Pierre Chauvin, N. Loundon, Annie Sergent-Allaoui, Muriel Houang, Alain Joannard, S. Schmerber, Bruno Delobel, Jacques Leman, Hubert Journel, Hélène Catros, Hélène Dollfus, Marie-Madeleine Eliot, Albert David, C. Calais, Valérie Drouin‐Garraud, Marie-Françoise Obstoy, Patrice Tran Ba Huy, Didier Lacombe, F Duriez, Christine Francannet, Pierre Bitoun, Christine Petit, Éréa-Noël Garabédian, Rémy Couderc, Sandrine Marlin, Françoise Denoyelle
Udgivet 2006Artigo -
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Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis af Crystel Bonnet, M’hamed Grati, Sandrine Marlin, Jacqueline Levilliers, Jean-Pierre Hardelin, M. Parodi, Magali Niasme-Grare, Diana Zélénika, Marc Delépine, Delphine Feldmann, Laurence Jonard, A. Amraoui, Dominique Weil, Bruno Delobel, C. Vincent, Hélène Dollfus, Marie-Madeleine Eliot, Albert David, C. Calais, Jacqueline Vigneron, B. Montaut-Verient, Dominique Bonneau, Jacques Dubin, Christel Thauvin, Alain Duvillard, Christine Francannet, T. Mom, Didier Lacombe, F Duriez, Valérie Drouin‐Garraud, Marie-Françoise Thuillier-Obstoy, Sabine Sigaudy, Anne-Marie Frances, Patrick Collignon, Georges Challe, Rémy Couderc, Mark Lathrop, José‐Alain Sahel, Jean Weissenbach, Christine Petit, Françoise Denoyelle
Udgivet 2011Artigo
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