Lower Frequency of HLA-DRB1 Type 1 Diabetes Risk Alleles in Pediatric Patients with MODY

Por Urrutia, Inés, Martínez, Rosa, López-Euba, Tamara, Velayos, Teresa, Martínez de LaPiscina, Idoia, Bilbao, José Ramón, Rica, Itxaso, Castaño, Luis
Publicado no PLoS One (2017)

QOS-27 10 YEARS REVIEW OF ENDOCRINOLOGICAL LATE EFFECTS IN SPANISH PATIENTS WITH PRIMARY BRAIN TUMORS IN A TERTIARY HOSPITAL

Por Garcia Ariza, Miguel, Portillo Najera, Nancy, Gonzalez Camacho, Usune, Rubio Rojas, Raquel, Vela De Sojo, Amaya, Rica, Itxaso, Astigarraga, Itziar, Navajas, Aurora
Publicado no Neuro Oncol (2016)

Exploring the diabetogenicity of the HLA-B18-DR3 CEH: independent association with T1D genetic risk close to HLA-DOA

Por Santin, Izortze, Castellanos-Rubio, Ainara, Aransay, Ana María, Gutierrez, Galder, Gaztambide, Sonia, Rica, Itxaso, Vicario, Jose Luis, Noble, Janelle A., Castaño, Luis, Bilbao, Jose Ramon
Publicado no Genes Immun (2009)

Evolutionary Analyses of Entire Genomes Do Not Support the Association of mtDNA Mutations with Ras/MAPK Pathway Syndromes

Por Gómez-Carballa, Alberto, Cerezo, María, Balboa, Emilia, Heredia, Claudia, Castro-Feijóo, Lidia, Rica, Itxaso, Barreiro, Jesús, Eirís, Jesús, Cabanas, Paloma, Martínez-Soto, Isabel, Fernández-Toral, Joaquín, Castro-Gago, Manuel, Pombo, Manuel, Carracedo, Ángel, Barros, Francisco, Salas, Antonio
Publicado em 2011

Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)(2)D serum levels are associated with PHEX mutation...

Por Morey, Marcos, Castro-Feijóo, Lidia, Barreiro, Jesús, Cabanas, Paloma, Pombo, Manuel, Gil, Marta, Bernabeu, Ignacio, Díaz-Grande, José M, Rey-Cordo, Lourdes, Ariceta, Gema, Rica, Itxaso, Nieto, José, Vilalta, Ramón, Martorell, Loreto, Vila-Cots, Jaime, Aleixandre, Fernando, Fontalba, Ana, Soriano-Guillén, Leandro, García-Sagredo, José M, García-Miñaur, Sixto, Rodríguez, Berta, Juaristi, Saioa, García-Pardos, Carmen, Martínez-Peinado, Antonio, Millán, José M, Medeira, Ana, Moldovan, Oana, Fernandez, Angeles, Loidi, Lourdes
Publicado em 2011

Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis

Por Garin, Intza, Edghill, Emma L., Akerman, Ildem, Rubio-Cabezas, Oscar, Rica, Itxaso, Locke, Jonathan M., Maestro, Miguel Angel, Alshaikh, Adnan, Bundak, Ruveyde, del Castillo, Gabriel, Deeb, Asma, Deiss, Dorothee, Fernandez, Juan M., Godbole, Koumudi, Hussain, Khalid, O’Connell, Michele, Klupa, Thomasz, Kolouskova, Stanislava, Mohsin, Fauzia, Perlman, Kusiel, Sumnik, Zdenek, Rial, Jose M., Ugarte, Estibaliz, Vasanthi, Thiruvengadam, Johnstone, Karen, Flanagan, Sarah E., Martínez, Rosa, Castaño, Carlos, Patch, Ann-Marie, Fernández-Rebollo, Eduardo, Raile, Klemens, Morgan, Noel, Harries, Lorna W., Castaño, Luis, Ellard, Sian, Ferrer, Jorge, de Nanclares, Guiomar Perez, Hattersley, Andrew T.
Publicado em 2010