Torthaí cuardaigh - Montserrat Rodriguez‐Ballesteros

  • 1 - 7 toradh as 7 á dtaispeáint
Beachtaigh na torthaí
  1. 1
    Effects of BDNF polymorphism and physical activity on episodic memory in the elderly: a cross sectional study

    Effects of BDNF polymorphism and physical activity on episodic memory in the elderly: a cross sectional study de réir Anne Canivet, Cédric T. Albinet, Nathalie André, Jean Pylouster, Montserrat Rodriguez‐Ballesteros, Alain Kitzis, Michel Audiffren

    Foilsithe / Cruthaithe 2015
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  2. 2
    Abnormal Cochlear Potentials from Deaf Patients with Mutations in the Otoferlin Gene

    Abnormal Cochlear Potentials from Deaf Patients with Mutations in the Otoferlin Gene de réir Rosamaria Santarelli, Ignacio del Castillo, Montserrat Rodriguez‐Ballesteros, Pietro Scimemi, Elona Cama, Edoardo Arslan, Arnold Starr

    Foilsithe / Cruthaithe 2009
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  3. 3
    Auditory neuropathy in patients carrying mutations in the otoferlin gene (<i>OTOF</i>)

    Auditory neuropathy in patients carrying mutations in the otoferlin gene (<i>OTOF</i>) de réir Montserrat Rodriguez‐Ballesteros, Francisco Castillo, Yolanda Martín, Miguel A. Moreno‐Pelayo, Constantino Morera, Félix Prieto, Jaime Marco, Antonio Ventura, Jaime Gallo‐Terán, Carmelo Morales‐Angulo, Cristina Navas, Germán Trinidad, M. Cruz Tapia, Felipe Moreno, Ignacio del Castillo

    Foilsithe / Cruthaithe 2003
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  4. 4
    Tryptophan‐rich basic protein (<scp>WRB</scp>) mediates insertion of the tail‐anchored protein otoferlin and is required for hair cell exocytosis and hearing

    Tryptophan‐rich basic protein (<scp>WRB</scp>) mediates insertion of the tail‐anchored protein otoferlin and is required for hair cell exocytosis and hearing de réir Christian Vogl, Iliana Panou, Gulnara Yamanbaeva, Carolin Wichmann, Sara J. Mangosing, Fabio Vilardi, Artur A. Indzhykulian, Tina Pangršič, Rosamaria Santarelli, Montserrat Rodriguez‐Ballesteros, Thomas Weber, Sangyong Jung, María Elena Cantú-Cárdenas, Xudong Wu, Sonja M. Wojcik, Kelvin Y. Kwan, Ignacio del Castillo, Blanche Schwappach, Nicola Strenzke, David P. Corey, Shuh‐Yow Lin, Tobias Moser

    Foilsithe / Cruthaithe 2016
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  5. 5
    A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (<i>OTOF</i>) in subjects with nonsyndromic hearing impairment and auditory neuropathy

    A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (<i>OTOF</i>) in subjects with nonsyndromic hearing impairment and auditory neuropathy de réir Montserrat Rodriguez‐Ballesteros, Raúl Reynoso, M. A. Gil Olarte, Manuela Villamar, Constantino Morera, Rosamaria Santarelli, Edoardo Arslan, Carme Medá, Carlos Curet, Christiane Völter, Manuel Sainz-Quevedo, Pierangela Castorina, Umberto Ambrosetti, Stefano Berrettini, Klemens Frei, Socorro Tedín, Janine Smith, M. Cruz Tapia, Laura Cavallé, Nancy Gélvez, Paola Primignani, Elena Gómez-Rosas, Mirta Martín, Miguel A. Moreno‐Pelayo, Marta Lucía Tamayo, José Moreno-Barral, Felipe Moreno, Ignacio del Castillo

    Foilsithe / Cruthaithe 2008
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  6. 6
    A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

    A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impai... de réir Francisco Castillo, Montserrat Rodriguez‐Ballesteros, Araceli Álvarez, Tim Hutchin, Emanuela Leonardi, Camila Andréa de Oliveira, Héla Azaiez, Zippora Brownstein, Matthew R. Avenarius, Sandrine Marlin, Arti Pandya, Hashem Shahin, Kirby Siemering, Dominique Weil, Wim Wuyts, Luis A. Aguirre, Y. Martin, Miguel A. Moreno‐Pelayo, Manuela Villamar, Karen B. Avraham, H H Dahl, Moien Kanaan, W E Nance, Christine Petit, Richard J. Smith, Guy Van Camp, Edi Lúcia Sartorato, Alessandra Murgia, Felipe Moreno, Ignacio del Castillo

    Foilsithe / Cruthaithe 2005
    Faigh an téacs iomlán Faigh an téacs iomlán
    Carta
    Cuir le mo chuid Ceanán
    Sábháilte in:
  7. 7
    Phenotype and genotype analysis of a French cohort of 119 patients with CHARGE syndrome

    Phenotype and genotype analysis of a French cohort of 119 patients with CHARGE syndrome de réir Marine Legendre, Véronique Abadie, Tania Attié‐Bitach, Nicole Philip, Tiffany Busa, Dominique Bonneau, Estelle Colin, Hélène Dollfus, Didier Lacombe, Annick Toutain, Sophie Blesson, Sophie Julia, Dominique Martin–Coignard, David Geneviève, Bruno Leheup, Sylvie Odent, Pierre‐Simon Jouk, Sandra Mercier, Laurence Faivre, Catherine Vincent‐Delorme, Christine Francannet, Sophie Naudion, Michèle Mathieu‐Dramard, Marie‐Ange Delrue, Alice Goldenberg, Delphine Héron, Philippe Parent, Renaud Touraine, Valérie Layet, Damien Sanlaville, Chloé Quēlin, Sébastien Moutton, Mélanie Fradin, Aurélia Jacquette, Sabine Sigaudy, Lucile Pinson, Pierre Sarda, Anne‐Marie Guerrot, Massimiliano Rossi, Alice Masurel‐Paulet, Salima El Chehadeh, Xavier Piguel, Montserrat Rodriguez‐Ballesteros, Stéphanie Ragot, Stanislas Lyonnet, Frédéric Bilan, Brigitte Gilbert‐Dussardier

    Foilsithe / Cruthaithe 2017
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:

Uirlisí cuardaigh: