Resultados da busca - D M Roden

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  1. 1
    Genetics of acquired long QT syndrome

    Genetics of acquired long QT syndrome por D M Roden

    Publicado em 2005
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  2. 2
    Genomic Medicine, Precision Medicine, Personalized Medicine: What’s in a Name?

    Genomic Medicine, Precision Medicine, Personalized Medicine: What’s in a Name? por D M Roden, Rachel F. Tyndale

    Publicado em 2013
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  3. 3
    Electronic Medical Records as a Tool in Clinical Pharmacology: Opportunities and Challenges

    Electronic Medical Records as a Tool in Clinical Pharmacology: Opportunities and Challenges por D M Roden, Hua Xu, Joshua C. Denny, Russell A. Wilke

    Publicado em 2012
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  4. 4
    Pharmacogenomics: Application to the Management of Cardiovascular Disease

    Pharmacogenomics: Application to the Management of Cardiovascular Disease por J. A. Johnson, Larisa H. Cavallari, A L Beitelshees, Joshua P. Lewis, Alan R. Shuldiner, D M Roden

    Publicado em 2011
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  5. 5
    Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes

    Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes por Andrea H. Ramirez, Christian M. Shaffer, Jessica Delaney, David Sexton, Shawn Levy, Mark J. Rieder, D A Nickerson, Alfred L. George, D M Roden

    Publicado em 2012
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  6. 6
    Clinical Pharmacogenetics Implementation Consortium Guidelines for Cytochrome P450-2C19 (CYP2C19) Genotype and Clopidogrel Therapy

    Clinical Pharmacogenetics Implementation Consortium Guidelines for Cytochrome P450-2C19 (CYP2C19) Genotype and Clopidogrel Therapy por Stuart A. Scott, Katrin Sangkuhl, E E Gardner, Catherine M. Stein, Jean‐Sébastien Hulot, J. A. Johnson, D M Roden, Teri E. Klein, Alan R. Shuldiner

    Publicado em 2011
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  7. 7
    Detecting Drug Interactions From Adverse-Event Reports: Interaction Between Paroxetine and Pravastatin Increases Blood Glucose Levels

    Detecting Drug Interactions From Adverse-Event Reports: Interaction Between Paroxetine and Pravastatin Increases Blood Glucose Levels por Nicholas P. Tatonetti, Joshua C. Denny, S. Murphy, G H Fernald, G. Krishnan, Vı́ctor Castro, Patrick Yue, P S Tsau, Isaac S. Kohane, D M Roden, Russ B. Altman

    Publicado em 2011
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  8. 8
    Clinical Pharmacogenetics Implementation Consortium Guidelines for CYP2C19 Genotype and Clopidogrel Therapy: 2013 Update

    Clinical Pharmacogenetics Implementation Consortium Guidelines for CYP2C19 Genotype and Clopidogrel Therapy: 2013 Update por Stuart A. Scott, Katrin Sangkuhl, Catherine M. Stein, Jean‐Sébastien Hulot, Jessica L. Mega, D M Roden, Teri E. Klein, Marc S. Sabatine, Julie A. Johnson, Alan R. Shuldiner

    Publicado em 2013
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  9. 9
    Optimizing Drug Outcomes Through Pharmacogenetics: A Case for Preemptive Genotyping

    Optimizing Drug Outcomes Through Pharmacogenetics: A Case for Preemptive Genotyping por Jonathan S. Schildcrout, Joshua C. Denny, Erica Bowton, W. Gregg, Jill M. Pulley, Melissa Basford, James D. Cowan, Hai-liang Xu, Andrea H. Ramirez, Dana C. Crawford, Marylyn D. Ritchie, Josh F. Peterson, Daniel R. Masys, Russell A. Wilke, D M Roden

    Publicado em 2012
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  10. 10
    The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1 and Simvastatin-Induced Myopathy: 2014 Update

    The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1 and Simvastatin-Induced Myopathy: 2014 Update por Laura B. Ramsey, Samuel G. Johnson, Kelly E. Caudle, Cyrine E. Haidar, Deepak Voora, Russell A. Wilke, Whitney D. Maxwell, Howard L. McLeod, Ronald M. Krauss, D M Roden, QiPing Feng, Rhonda M. Cooper‐DeHoff, Li Gong, Teri E. Klein, Mia Wadelius, Mikko Niemi

    Publicado em 2014
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  11. 11
    Operational Implementation of Prospective Genotyping for Personalized Medicine: The Design of the Vanderbilt PREDICT Project

    Operational Implementation of Prospective Genotyping for Personalized Medicine: The Design of the Vanderbilt PREDICT Project por Jill M. Pulley, Joshua C. Denny, JF Peterson, Gordon R. Bernard, C. L. Vnencak-Jones, Andrea H. Ramirez, Jessica Delaney, Erica Bowton, Kevin B. Johnson, Dana C. Crawford, J. Schildcrout, Daniel R. Masys, Holli H. Dilks, Russell A. Wilke, Ellen Wright Clayton, E. Shultz, Michael Laposata, John McPherson, Jim Jirjis, D M Roden

    Publicado em 2012
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  12. 12
    Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study

    Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study por Elijah R. Behr, Eleonora Savio‐Galimberti, Julien Barc, Anders G. Holst, Evmorfia Petropoulou, Bram P. Prins, Javad Jabbari, Margherita Torchio, Myriam Berthet, Yuka Mizusawa, Tao Yang, Eline A. Nannenberg, Federica Dagradi, Peter Weeke, Rachel Bastiaenan, Michael J. Ackerman, Stig Haunsø, Antoine Leenhardt, Stefan Kääb, Vincent Probst, Richard Redon, Sanjay Sharma, Arthur A.M. Wilde, Jacob Tfelt‐Hansen, Peter J. Schwartz, D M Roden, Connie R. Bezzina, Morten S. Olesen, Dawood Darbar, Pascale Guicheney, Lia Crotti, Yalda Jamshidi

    Publicado em 2015
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  13. 13
    Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

    Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation por Stefan Kääb, Dawood Darbar, Charlotte van Noord, Josée Dupuis, Arne Pfeufer, Chris Newton-Cheh, Renate B. Schnabel, S Makino, Moritz F. Sinner, Prince J. Kannankeril, Britt Maria Beckmann, Subbarao Choudry, Brian S. Donahue, Jan Heeringa, Siegfried Perz, Kathryn L. Lunetta, Martin G. Larson, Daniel Levy, Calum A. MacRae, Jeremy N. Ruskin, A. Wacker, Albert Schömig, H.‐Erich Wichmann, Gerhard Steinbeck, Thomas Meitinger, André G. Uitterlinden, Jacqueline C.M. Witteman, D M Roden, Emelia J. Benjamin, Patrick T. Ellinor

    Publicado em 2008
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