Search Results - Piñeros-Hernández, Laura B

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  1. 1
    A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy

    A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy by Silva, Claudia Tamar, Zorkoltseva, Irina V, Niemeijer, Maartje N, van den Berg, Marten E, Amin, Najaf, Demirkan, Ayşe, van Leeuwen, Elisa, Iglesias, Adriana I, Piñeros-Hernández, Laura B, Restrepo, Carlos M, Kors, Jan A, Kirichenko, Anatoly V, Willemsen, Rob, Oostra, Ben A, Stricker, Bruno H, Uitterlinden, André G, Axenovich, Tatiana I, van Duijn, Cornelia M, Isaacs, Aaron

    Published in BMC medical genomics
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  2. 2
    Correction: Uveitis and Multiple Sclerosis: Potential Common Causal Mutations

    Correction: Uveitis and Multiple Sclerosis: Potential Common Causal Mutations by de-la-Torre, Alejandra, Silva-Aldana, Claudia T., Muñoz-Ortiz, Juliana, Piñeros-Hernández, Laura B., Otero-Marquez, Oscar, Domínguez, Alejandra, Faciolince, León A., Arcos-Holzinger, Mauricio, Mastronardi, Claudio, Contreras-Bravo, Nora Constanza, Restrepo, Carlos Martín, Arcos-Burgos, Mauricio

    Published in Molecular neurobiology
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  3. 3
    Internal jugular access using pocket ultrasound in a simulated model: comparison between biplane and monoplane visualization techniques

    Internal jugular access using pocket ultrasound in a simulated model: comparison between biplane and monoplane visualization techniques by Garzón, Jair Antonio Ruiz, López, Gloria Catalina Zuluaga, Piñeros-Hernandez, Laura B., Martínez, Yury Forlan Bustos

    Published in The ultrasound journal
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  4. 4
    Uveitis and Multiple Sclerosis: Potential Common Causal Mutations

    Uveitis and Multiple Sclerosis: Potential Common Causal Mutations by de-la-Torre, Alejandra, Silva-Aldana, Claudia T., Muñoz-Ortiz, Juliana, Piñeros-Hernández, Laura B., Otero, Oscar, Domínguez, Alejandra, Faciolince, León A., Arcos-Holzinger, Mauricio, Mastronardi, Claudio, Contreras-Bravo, Nora Constanza, Restrepo, Carlos Martín, Arcos-Burgos, Mauricio

    Published in Molecular neurobiology
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  5. 5
    A Pharmacogenetic Study of CYP2C19 in Acute Coronary Syndrome Patients of Colombian Origin Reveals New Polymorphisms Potentially Related to Clopidogrel Therapy

    A Pharmacogenetic Study of CYP2C19 in Acute Coronary Syndrome Patients of Colombian Origin Reveals New Polymorphisms Potentially Related to Clopidogrel Therapy by Angulo-Aguado, Mariana, Panche, Karen, Tamayo-Agudelo, Caroll Andrea, Ruiz-Torres, Daniel-Armando, Sambracos-Parrado, Santiago, Niño-Orrego, Maria Jose, Páez, Nathaly, Piñeros-Hernandez, Laura B, Castillo-León, Luisa-Fernanda, Pardo-Oviedo, Juan Mauricio, Abaunza, Katherine Parra, Laissue, Paul, Contreras, Nora, Calderón-Ospina, Carlos Alberto, Fonseca-Mendoza, Dora Janeth

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