Search Results - Repáraz Andrade, Alfredo

  • Showing 1 - 7 results of 7
Refine Results
  1. 1
    Clear cell clusters in the kidney: a rare finding that should not be misdiagnosed as renal cell carcinoma

    Clear cell clusters in the kidney: a rare finding that should not be misdiagnosed as renal cell carcinoma by Ortiz-Rey, José-Antonio, Fachal, Carmen, Juaneda-Magdalena, Laura, Muñoz-Martín, Mónica, Repáraz-Andrade, Alfredo, Teijeira, Susana, Lamas-Barreiro, José-María, Almuster-Domínguez, Sheila, San Miguel-Fraile, Pilar, Gómez-de María, Carolina

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  2. 2
    The effect of copy number variations in chromosome 16p on body weight in patients with intellectual disability

    The effect of copy number variations in chromosome 16p on body weight in patients with intellectual disability by Gimeno-Ferrer, Fátima, Albuquerque, David, Guzmán Luján, Carola, Marcaida Benito, Goitzane, Torreira Banzas, Cristina, Repáraz-Andrade, Alfredo, Ballesteros Cogollos, Virginia, Aleu Pérez-Gramunt, Montserrat, Galán Gómez, Enrique, Quintela, Inés, Rodríguez-López, Raquel

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

    Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients by Cabanillas, Rubén, Diñeiro, Marta, Cifuentes, Guadalupe A, Castillo, David, Pruneda, Patricia C, Álvarez, Rebeca, Sánchez-Durán, Noelia, Capín, Raquel, Plasencia, Ana, Viejo-Díaz, Mónica, García-González, Noelia, Hernando, Inés, Llorente, José L, Repáraz-Andrade, Alfredo, Torreira-Banzas, Cristina, Rosell, Jordi, Govea, Nancy, Gómez-Martínez, Justo Ramón, Núñez-Batalla, Faustino, Garrote, José A, Mazón-Gutiérrez, Ángel, Costales, María, Isidoro-García, María, García-Berrocal, Belén, Ordóñez, Gonzalo R, Cadiñanos, Juan

    Published in BMC medical genomics
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    ABCB4 variants in adult patients with cholestatic disease are frequent and underdiagnosed

    ABCB4 variants in adult patients with cholestatic disease are frequent and underdiagnosed by Avena, Antonella, Puggelli, Sandro, Morris, Michael, Cerny, Andreas, Andrade, Alfredo Repáraz, Pareti, Emmanuela, Bihl, Florian, Cassatella, Daniele, Moix, Isabelle, Merlo, Elisabetta, Rougemont, Anne-Laure, Majno-Hurst, Pietro, Vergani, Diego, Mieli-Vergani, Giorgina, Terziroli Beretta-Piccoli, Benedetta

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  5. 5
    Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy

    Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy by Ochoa, Juan Pablo, Sabater-Molina, María, García-Pinilla, José Manuel, Mogensen, Jens, Restrepo-Córdoba, Alejandra, Palomino-Doza, Julián, Villacorta, Eduardo, Martinez-Moreno, Marina, Ramos-Maqueda, Javier, Zorio, Esther, Peña-Peña, Maria L., García-Granja, Pablo E., Rodríguez-Palomares, José F., Cárdenas-Reyes, Ivonne J., de la Torre-Carpente, María M., Bautista-Pavés, Alicia, Akhtar, Mohammed M., Cicerchia, Marcos N., Bilbao-Quesada, Raquel, Mogollón-Jimenez, Maria Victoria, Salazar-Mendiguchía, Joel, Mesa Latorre, José M., Arnaez, Blanca, Olavarri-Miguel, Ivan, Fuentes-Cañamero, María E., Lamounier, Arsonval, Pérez Ruiz, José María, Climent-Payá, Vicente, Pérez-Sanchez, Inmaculada, Trujillo-Quintero, Juan P., Lopes, Luis R., Repáraz-Andrade, Alfredo, Marín-Iglesias, Rosario, Rodriguez-Vilela, Alejandro, Sandín-Fuentes, María, Garrote, Jose A., Cortel-Fuster, Alejandro, Lopez-Garrido, Miguel, Fontalba-Romero, Ana, Ripoll-Vera, Tomás, Llano-Rivas, Isabel, Fernandez-Fernandez, Xusto, Isidoro-García, María, Garcia-Giustiniani, Diego, Barriales-Villa, Roberto, Ortiz-Genga, Martín, García-Pavía, Pablo, Elliott, Perry M., Gimeno, Juan R., Monserrat, Lorenzo

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  6. 6
    Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant

    Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant by Lamounier Junior, Arsonval, Guitián González, Alba, Rodríguez Vilela, Alejandro, Repáraz Andrade, Alfredo, Rubio Alcaide, Álvaro, Berta Sousa, Ana, Benito López, Carmen, Alonso García, Diego, Fernández Ferro, Germán, Cruz, Inês, Cárdenas Reyes, Ivonne Johana, Salazar-Mendiguchía García, Joel, Larrañaga-Moreira, José María, Ochoa, Juan Pablo, Palomino-Doza, Julián, de la Higuera Romero, Luis, Nicolás Cicerchia, Marcos, Restrepo Córdoba, María Alejandra, Peña-Peña, María Luisa, Noël Brögger, Maria, Loureiro, Marilia, Mogollón Jiménez, María Victoria, Bilbao Quesada, Raquel, Franco Gutiérrez, Raúl, García Hernández, Soledad, Ripoll-Vera, Tomás, Fernández, Xusto, Azevedo, Olga, García Pavía, Pablo, Lopes, Luis R., Ortiz, Martín, Brito, Dulce, Barriales-Villa, Roberto, Monserrat Iglesias, Lorenzo

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  7. 7
    Neurodevelopment disorders and Array-CGH: Sensitivity and specificity using a checklist as criteria for performing a genetic test

    Neurodevelopment disorders and Array-CGH: Sensitivity and specificity using a checklist as criteria for performing a genetic test by Puentes, Alfonso Amado, Reparaz Andrade, Alfredo, del Campo García, Aida, Blanco Barca, Manuel Oscar, Banzas, Cristina Torreira, Campo Pérez, Victor del, Fernández Lorenzo, José Ramón

    Get full text
    Article
    Save to List
    Saved in:

Search Tools: