Search Results - García-Piñero, Alfons

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  1. 1
    SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome

    SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome by Hanchate, Naresh Kumar, Giacobini, Paolo, Lhuillier, Pierre, Parkash, Jyoti, Espy, Cécile, Fouveaut, Corinne, Leroy, Chrystel, Baron, Stéphanie, Campagne, Céline, Vanacker, Charlotte, Collier, Francis, Cruaud, Corinne, Meyer, Vincent, García-Piñero, Alfons, Dewailly, Didier, Cortet-Rudelli, Christine, Gersak, Ksenija, Metz, Chantal, Chabrier, Gérard, Pugeat, Michel, Young, Jacques, Hardelin, Jean-Pierre, Prevot, Vincent, Dodé, Catherine

    Published in PLoS genetics
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  2. 2
    Persistent allergic rhinitis has a moderate impact on the sense of smell, depending on both nasal congestion and inflammation

    Persistent allergic rhinitis has a moderate impact on the sense of smell, depending on both nasal congestion and inflammation by Guilemany, José Maria, García-Piñero, Alfons, Alobid, Isam, Cardelús, Sara, Centellas, Silvia, Bartra, Joan, Valero, Antonio, Picado, César, Mullol, Joaquim

    Published in The Laryngoscope
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  3. 3
    A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

    A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes by Sarfati, Julie, Guiochon-Mantel, Anne, Rondard, Philippe, Arnulf, Isabelle, Garcia-Piñero, Alfons, Wolczynski, Slawomir, Brailly-Tabard, Sylvie, Bidet, Maud, Ramos-Arroyo, Maria, Mathieu, Michèle, Lienhardt-Roussie, Anne, Morgan, Graeme, Turki, Zinet, Bremont, Catherine, Lespinasse, James, Du Boullay, Hélène, Chabbert-Buffet, Nathalie, Jacquemont, Sébastien, Reach, Gérard, De Talence, Nicole, Tonella, Paolo, Conrad, Bernard, Despert, Francois, Delobel, Bruno, Brue, Thierry, Bouvattier, Claire, Cabrol, Sylvie, Pugeat, Michel, Murat, Arnaud, Bouchard, Philippe, Hardelin, Jean-Pierre, Dodé, Catherine, Young, Jacques

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  4. 4
    A Comparative Phenotypic Study of Kalimann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

    A Comparative Phenotypic Study of Kalimann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes by SARFATI, Julie, GUIOCHON-MANTEL, Anne, LIENHARDT-ROUSSIE, Anne, MORGAN, Graeme, TURKI, Zinet, BREMONT, Catherine, LESPINASSE, James, DU BOULLAY, Hélène, CHABBERT-BUFFET, Nathalie, JACQUEMONT, Sébastien, REACH, Gerard, DE TALENCE, Nicole, RONDARD, Philippe, TONELLA, Paolo, CONRAD, Bernard, DESPERT, Francois, DELOBEL, Bruno, BRUE, Thierry, BOUVATTIER, Claire, CABROL, Sylvie, PUGEAT, Michel, MURAT, Arnaud, BOUCHARD, Philippe, ARNULF, Isabelle, HARDELIN, Jean-Pierre, DODE, Catherine, YOUNG, Jacques, GARCIA-PINERO, Alfons, WOLCZYNSKI, Slawomir, BRAILLY-TABARD, Sylvie, BIDET, Maud, RAMOS-ARROYO, Maria, MATHIEU, Michèle

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