Resultats de la cerca - Michael J. Ackerman

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  1. 1
    The Long QT Syndrome: Ion Channel Diseases of the Heart

    The Long QT Syndrome: Ion Channel Diseases of the Heart per Michael J. Ackerman

    Publicat 1998
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  2. 2
    The Visible Human Project

    The Visible Human Project per Michael J. Ackerman

    Publicat 1999
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  3. 3
    State of Postmortem Genetic Testing Known as the Cardiac Channel Molecular Autopsy in the Forensic Evaluation of Unexplained Sudden Cardiac Death in the Young

    State of Postmortem Genetic Testing Known as the Cardiac Channel Molecular Autopsy in the Forensic Evaluation of Unexplained Sudden Cardiac Death in the Young per Michael J. Ackerman

    Publicat 2009
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  4. 4
    Genetic Testing for Potentially Lethal, Highly Treatable Inherited Cardiomyopathies/Channelopathies in Clinical Practice

    Genetic Testing for Potentially Lethal, Highly Treatable Inherited Cardiomyopathies/Channelopathies in Clinical Practice per David J. Tester, Michael J. Ackerman

    Publicat 2011
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  5. 5
    Genetic testing in heritable cardiac arrhythmia syndromes

    Genetic testing in heritable cardiac arrhythmia syndromes per John R. Giudicessi, Michael J. Ackerman

    Publicat 2012
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  6. 6
    Beyond the Cardiac Myofilament: Hypertrophic Cardiomyopathy- Associated Mutations in Genes that Encode Calcium-Handling Proteins

    Beyond the Cardiac Myofilament: Hypertrophic Cardiomyopathy- Associated Mutations in Genes that Encode Calcium-Handling Proteins per Andrew P. Landstrom, Michael J. Ackerman

    Publicat 2012
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  7. 7
    Azithromycin and risk of sudden cardiac death: Guilty as charged or falsely accused?

    Azithromycin and risk of sudden cardiac death: Guilty as charged or falsely accused? per John R. Giudicessi, Michael J. Ackerman

    Publicat 2013
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  8. 8
    Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes

    Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes per John R. Giudicessi, Michael J. Ackerman

    Publicat 2012
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  9. 9
    Potassium-channel mutations and cardiac arrhythmias—diagnosis and therapy

    Potassium-channel mutations and cardiac arrhythmias—diagnosis and therapy per John R. Giudicessi, Michael J. Ackerman

    Publicat 2012
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  10. 10
    Genetics of Long QT Syndrome

    Genetics of Long QT Syndrome per David J. Tester, Michael J. Ackerman

    Publicat 2014
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  11. 11
    Genotype- and Phenotype-Guided Management of Congenital Long QT Syndrome

    Genotype- and Phenotype-Guided Management of Congenital Long QT Syndrome per John R. Giudicessi, Michael J. Ackerman

    Publicat 2013
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  12. 12
    Defining a New Paradigm for Human Arrhythmia Syndromes

    Defining a New Paradigm for Human Arrhythmia Syndromes per Michael J. Ackerman, Peter J. Mohler

    Publicat 2010
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  13. 13
    The Molecular Autopsy: Should the Evaluation Continue After the Funeral?

    The Molecular Autopsy: Should the Evaluation Continue After the Funeral? per David J. Tester, Michael J. Ackerman

    Publicat 2012
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  14. 14
    Mutation Type Is Not Clinically Useful in Predicting Prognosis in Hypertrophic Cardiomyopathy

    Mutation Type Is Not Clinically Useful in Predicting Prognosis in Hypertrophic Cardiomyopathy per Andrew P. Landstrom, Michael J. Ackerman

    Publicat 2010
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  15. 15
    QTc: how long is too long?

    QTc: how long is too long? per Jonathan N. Johnson, Michael J. Ackerman

    Publicat 2009
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  16. 16
    Return to play? Athletes with congenital long QT syndrome

    Return to play? Athletes with congenital long QT syndrome per Jonathan N. Johnson, Michael J. Ackerman

    Publicat 2012
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  17. 17
    Prevalence and Potential Genetic Determinants of Sensorineural Deafness in <i>KCNQ1</i> Homozygosity and Compound Heterozygosity

    Prevalence and Potential Genetic Determinants of Sensorineural Deafness in <i>KCNQ1</i> Homozygosity and Compound Heterozygosity per John R. Giudicessi, Michael J. Ackerman

    Publicat 2013
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  18. 18
    The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy

    The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy per Peter J. Schwartz, Michael J. Ackerman

    Publicat 2013
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  19. 19
    Sudden infant death syndrome: How significant are the cardiac channelopathies?

    Sudden infant death syndrome: How significant are the cardiac channelopathies? per David J. Tester, Michael J. Ackerman

    Publicat 2005
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  20. 20
    Cardiac sympathetic denervation in the prevention of genetically mediated life-threatening ventricular arrhythmias

    Cardiac sympathetic denervation in the prevention of genetically mediated life-threatening ventricular arrhythmias per Peter J. Schwartz, Michael J. Ackerman

    Publicat 2022
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