Search Results - Trujillo-Quintero, P.

  • Showing 1 - 6 results of 6
Refine Results
  1. 1
    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:
  2. 2
    PND51 PATTERNS OF ANTIDEMENTIAL DRUG USE IN A GROUP OF PATIENTS FROM COLOMBIA

    PND51 PATTERNS OF ANTIDEMENTIAL DRUG USE IN A GROUP OF PATIENTS FROM COLOMBIA by Calvo-Torres, F., Bernal-Cobo, R., Trujillo-Quintero, P., Gaviria-Mendoza, A., Machado Alba, J.

    Published in Value in health
    Get full text
    Article
    Save to List
    Saved in:
  3. 3
    The role of TBX20 truncating variants in dilated and left ventricular non-compaction cardiomyopathy

    The role of TBX20 truncating variants in dilated and left ventricular non-compaction cardiomyopathy by Amor-Salamanca, A, Garcia-Cruz, L M, Rasoul, H, De Castro Campos, D, Limeres, J, Gimeno, J R, Garcia-Pinilla, J M, Basurte Elorz, M T, Bilbao-Quesada, R, Fuentes Canamero, M E, Moldovan, O, Trujillo-Quintero, J P, Morris-Hey, T, Savvatis, K, Ochoa, J P

    Published in European heart journal
    Get full text
    Article
    Save to List
    Saved in:
  4. 4
    602Sudden death risk in carriers of KCNH2 mutations. Influence of gender, location and type of mutation

    602Sudden death risk in carriers of KCNH2 mutations. Influence of gender, location and type of mutation by Garcia-Giustiniani, DA, Ochoa, JP, Ortiz-Genga, M., Barriales-Villa, R., Salazar-Mendiguchia, J., Cicerchia, M., Lamounier Junior, A., Rodriguez-Garrido, J., Barraza-Garcia, J., Cardenas-Reyes, I., Fernandez-Fernandez, X., Trujillo-Quintero, JP, Monserrat, L.

    Get full text
    Article
    Save to List
    Saved in:
  5. 5
    Case report: Identification of a novel variant p.Gly215Arg in the CHN1 gene causing Moebius syndrome

    Case report: Identification of a novel variant p.Gly215Arg in the CHN1 gene causing Moebius syndrome by Manso-Bazús, Carmen, Spataro, Nino, Gabau, Elisabeth, Beltrán-Salazar, Viviana P, Trujillo-Quintero, Juan Pablo, Capdevila, Nuria, Brunet-Vega, Anna, Baena, Neus, Jeyaprakash, A Arockia, Martinez-Glez, Victor, Ruiz, Anna

    Published in Frontiers in genetics
    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  6. 6
    Case report: Identification of a novel variant p.Gly215Arg in the CHN1 gene causing Moebius syndrome

    Case report: Identification of a novel variant p.Gly215Arg in the CHN1 gene causing Moebius syndrome by Manso-Bazús, Carmen, Spataro, Nino, Gabau, Elisabeth, Beltrán-Salazar, Viviana P, Trujillo-Quintero, Juan Pablo, Capdevila, Nuria, Brunet-Vega, Anna, Baena, Neus, Jeyaprakash, A Arockia, Martinez-Glez, Victor, Ruiz, Anna

    Published in Frontiers in genetics
    Get full text
    Report
    Save to List
    Saved in:

Search Tools: