Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss von del Castillo, F J, Rodríguez-Ballesteros, M, Martín, Y, Arellano, B, Gallo-Terán, J, Morales-Angulo, C, Ramírez-Camacho, R, Cruz Tapia, M, Solanellas, J, Martínez-Conde, A, Villamar, M, Moreno-Pelayo, M A, Moreno, F, del Castillo, I

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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... von del Castillo, F J, Rodríguez-Ballesteros, M, Álvarez, A, Hutchin, T, Leonardi, E, de Oliveira, C A, Azaiez, H, Brownstein, Z, Avenarius, M R, Marlin, S, Pandya, A, Shahin, H, Siemering, K R, Weil, D, Wuyts, W, Aguirre, L A, Martín, Y, Moreno-Pelayo, M A, Villamar, M, Avraham, K B, Dahl, H-H M, Kanaan, M, Nance, W E, Petit, C, Smith, R J H, Van Camp, G, Sartorato, E L, Murgia, A, Moreno, F, del Castillo, I

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Construction and Characterization of Mutations at Codon 751 of the Escherichia coli gyrB Gene That Confer Resistance to the Antimicrobial Peptide Microcin B17 and Alter the Activit... von del Castillo, F J, del Castillo, I, Moreno, F

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Los miRNAs como potenciales biomarcadores de las enfermedades oculares von Pinazo-Durán, M.D, Galbis-Estrada, C, Zanón-Moreno, V, García-Medina, J.J, Bendala-Tufanisco, E, Vinuesa-Silva, I, Benítez del Castillo, F.J

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THU0015 Genetic Analyses of Candidate Genes for Sapho Syndrome von Del Castillo, F. J, Ruiz-Palmero, L., Hurtado-Nédélec, M., Caniego, T., Kahn, M. F., Gómez-Rosas, E., Meyer, O., Chollet-Martin, S., Hayem, G.

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Characterization of the genes encoding the SheA haemolysin in Escherichia coli O157:H7 and Shigella flexneri 2a von del Castillo, Francisco J., Moreno, Felipe, del Castillo, Ignacio

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The Escherichia coli K‐12 sheA gene encodes a 34‐kDa secreted haemolysin von Del Castillo, Francisco J., Leal, Sandra C., Moreno, Felipe, Castillo, Ignacio del

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Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA(Ser(UCN)) gene von del Castillo, F J, Villamar, M, Moreno-Pelayo, M A, Almela, J J, Morera, C, Adiego, I, Moreno, F, del Castillo, I

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A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment von del Castillo, Francisco J, del Castillo, Ignacio, Villamar, Manuela, Moreno-Pelayo, Miguel A, Álvarez, Araceli, Tellería, Dolores, Menéndez, Ibis, Moreno, Felipe

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Secretion of the Escherichia coli K-12 SheA hemolysin is independent of its cytolytic activity von del Castillo, Francisco J, Moreno, Felipe, del Castillo, Ignacio

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Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF) von Rodríguez-Ballesteros, Montserrat, del Castillo, Francisco J., Martín, Yolanda, Moreno-Pelayo, Miguel A., Morera, Constantino, Prieto, Félix, Marco, Jaime, Morant, Antonio, Gallo-Terán, Jaime, Morales-Angulo, Carmelo, Navas, Cristina, Trinidad, Germán, Tapia, M. Cruz, Moreno, Felipe, Castillo, Ignacio del

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Lumbar herniated disks treated with a dynamic interspacer von Cueva-del Castillo Mendoza, J F, Franco-López, E A, Hinojosa-Sandoval, F, de León-Martínez, U A, Cueva-del Castillo Mendoza, F J

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Complex multiligament knee injury associated with patellar tendon rupture von Canales-Zamora, O A, Benítez-Romero, A, Mejía-Rohenes, L C, Mora-Ríos, F G, González-Gijón, O R, Cueva Del Castillo-Mendoza, J F

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Lesiones multiligamentarias de rodilla asociadas a ruptura de tendón rotuliano von Cueva Del Castillo-Mendoza, JF, González-Gijón, OR, Mora-Ríos, FG, Mejía-Rohenes, LC, Benítez-Romero, A, Canales-Zamora, OA

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THU0466 Unraveling the Genetic Basis of Familial SAPHO Syndrome with Next-Generation Sequencing von Del Castillo, F.J., Caniego, T., Hurtado-Nédélec, M., Chollet-Martín, S., Gόmez-Rosas, E., Kahn, M.-F., Meyer, O., Hayem, G.

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MicroRNAs as potential biomarkers of eye diseases von Pinazo-Durán, M D, Galbis-Estrada, C, Zanón-Moreno, V, García-Medina, J J, Bendala-Tufanisco, E, Vinuesa-Silva, I, Benítez del Castillo, F J

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Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNASer(UCN) gene von del Castillo, F J, Villamar, M, Moreno-Pelayo, M A, Almela, J J, Morera, C, Adiego, I, Moreno, F, del Castillo, I

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A novel deletion involving the connexin-30 gene, del(GJb6-d13s1854), found in frans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impai... von DEL CASTILLO, F. J, RODRIGUEZ-BALLESTEROS, M, PANDYA, A, SHAHIN, H, SIEMERING, K. R, WEIL, D, WUYTS, W, AGUIRRE, L. A, MARTIN, Y, MORENO-PELAYO, M. A, VILLAMAR, M, AVRAHAM, K. B, ALVAREZ, A, DAHL, H.-H. M, KANAAN, M, NANCE, W. E, PETIT, C, SMITH, R. J. H, VAN CAMP, G, SARTORATO, E. L, MURGIA, A, MORENO, F, DEL CASTILLO, I, HUTCHIN, T, LEONARDI, E, DE OLIVEIRA, C. A, AZAIEZ, H, BROWNSTEIN, Z, AVENARIUS, M. R, MARLIN, S

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Una idea frustrada : El Laboratorio Oceanográfico de Canarias (1927-1935) von MARTIN DEL CASTILLO, J. F

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Heteroplasmy for the 1555AG mutation in the mitochondrial 12S rRNA gene six Spanish families with non-syndromic hearing loss von del Castillo, FJ, Rodriguez-Ballesteros, M, Ma, Arellano, B, Gallo-Teran, J, Morales-Angulo, C, Ramirez-Camacho, R, Cruz Tapia, M, Solanellas, J, Ma, Villamar, M, Moreno-Pelayo, MA, Moreno, F, del Castillo, I

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