Search Results - Dzwiniel, Tara

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  1. 1
    Cardiomyopathies and Genetic Testing in Heart Failure: Role in Defining Phenotype-Targeted Approaches and Management

    Cardiomyopathies and Genetic Testing in Heart Failure: Role in Defining Phenotype-Targeted Approaches and Management by Yogasundaram, Haran, Alhumaid, Waleed, Dzwiniel, Tara, Christian, Susan, Oudit, Gavin Y.

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  2. 2
    P833: A novel cardiac genetic knowledge scale: Development and evaluation of face validity and concept validity

    P833: A novel cardiac genetic knowledge scale: Development and evaluation of face validity and concept validity by Christian, Susan, Baker, Amy, Dzwiniel, Tara, Borle, Kennedy, Mostafavi, Roya, Wand, Hannah, Slamon, Jill, Biesecker, Barbara, Yeates, Laura

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  3. 3
    How Much Is Enough? Weighing the Evidence for Mutation Pathogenicity

    How Much Is Enough? Weighing the Evidence for Mutation Pathogenicity by Dzwiniel, Tara L., MSc, Gilchrist, Dawna M., MD, FRCPC, FCCMG, Hume, Stacey, PhD, FCCMG

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  4. 4
    Abstract 14343: Early Genetic Screening and Cardiac Intervention in Patients With Genetic Cardiomyopathies Within a Multidisciplinary Care Model

    Abstract 14343: Early Genetic Screening and Cardiac Intervention in Patients With Genetic Cardiomyopathies Within a Multidisciplinary Care Model by Sadasivan, Chandu, Gagnon, Luke R, Wang, Kaiming, Hazra, Deepan, Dzwiniel, Tara, Christian, Susan, Thomas, Jissy, Chan, Anita Y, Paterson, David I, Tymchak, Wayne, Oudit, Gavin Y

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  5. 5
    Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot study

    Evaluation of face validity and core concepts of a novel knowledge scale for inherited heart disease: A pilot study by Christian, Susan, Dzwiniel, Tara, Baker, Amy, Biesecker, Barbara, Borle, Kennedy, Mostafavi, Roya, Slamon, Jillian, Wand, Hannah, Yeates, Laura

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  6. 6
    Uptake of Predictive Genetic Testing and Cardiac Evaluation for Children at Risk for an Inherited Arrhythmia or Cardiomyopathy

    Uptake of Predictive Genetic Testing and Cardiac Evaluation for Children at Risk for an Inherited Arrhythmia or Cardiomyopathy by Christian, Susan, Atallah, Joseph, Clegg, Robin, Giuffre, Michael, Huculak, Cathleen, Dzwiniel, Tara, Parboosingh, Jillian, Taylor, Sherryl, Somerville, Martin

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  7. 7
    Episodic Ataxia Secondary to CEP290 Compound Heterozygous Mutations: A Case Report

    Episodic Ataxia Secondary to CEP290 Compound Heterozygous Mutations: A Case Report by Hamed, Moath, Shetty, Aakash, Dzwiniel, Tara, Buller, Mark, Koskinen, Lotta, Suchowersky, Oksana

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  8. 8
    Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family

    Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family by Wang, Jing, Brautbar, Ariel, Chan, Alicia K., Dzwiniel, Tara, Li, Fang-yuan, Waters, Paula J., Graham, Brett H., Wong, Lee-Jun

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  9. 9
    Episodic Ataxia Secondary to CEP290 Compound Heterozygous Mutations: A Case Report

    Episodic Ataxia Secondary to CEP290 Compound Heterozygous Mutations: A Case Report by Hamed, Moath, Shetty, Aakash, Dzwiniel, Tara, Buller, Mark, Koskinen, Lotta, Suchowersky, Oksana

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