Search Results - "Saarel, Elizabeth V."

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    Pediatric Electrophysiology Device Needs: A Survey from the Pediatric and Congenital Electrophysiology Society Taskforce on Pediatric-Specific Devices by Dubin, Anne M, Bar-Cohen, Yaniv, Berul, Charles I, Cannon, Bryan C, Saarel, Elizabeth V, Shah, Maully J, Triedman, John K

    Published in Journal of the American Heart Association (15-11-2022)
    “…Background There are few US Food and Drug Administration (FDA)-approved devices specifically aimed at the pediatric patient with arrhythmia. This has led to a…”
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    Journal Article
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    Inappropriate ICD shocks in pediatrics and congenital heart disease patients: Risk factors and programming strategies by Garnreiter, Jason M., MD, Pilcher, Thomas A., MD, FHRS, Etheridge, Susan P., MD, FHRS, Saarel, Elizabeth V., MD, FHRS

    Published in Heart rhythm (01-05-2015)
    “…Background Inappropriate implantable cardioverter-defibrillator (ICD) shocks are a common and significant problem in pediatric patients and patients with…”
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    A Functional Assay for Sick Sinus Syndrome Genetic Variants by Jou, Chuanchau J., Arrington, Cammon B., Barnett, Spencer, Shen, Jiaxiang, Cho, Scott, Sheng, Xiaoming, McCullagh, Patrick C., Bowles, Neil E., Pribble, Chase M., Saarel, Elizabeth V., Pilcher, Thomas A., Etheridge, Susan P., Tristani-Firouzi, Martin

    Published in Cellular physiology and biochemistry (01-01-2017)
    “…Background/Aims: Congenital Sick Sinus Syndrome (SSS) is a disorder associated with sudden cardiac death due to severe bradycardia and prolonged pauses…”
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    The application of root mean square electrocardiography (RMS ECG) for the detection of acquired and congenital long QT syndrome by Lux, Robert L, Sower, Christopher Todd, Allen, Nancy, Etheridge, Susan P, Tristani-Firouzi, Martin, Saarel, Elizabeth V

    Published in PloS one (15-01-2014)
    “…Precise measurement of the QT interval is often hampered by difficulty determining the end of the low amplitude T wave. Root mean square electrocardiography…”
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    Long QT Syndrome in Children in the Era of Implantable Defibrillators by Etheridge, Susan P., MD, FACC, Sanatani, Shubhayan, MD, Cohen, Mitchell I., MD, FACC, Albaro, Cecilia A., MD, Saarel, Elizabeth V., MD, FACC, Bradley, David J., MD, FACC

    “…Long QT Syndrome in Children in the Era of Implantable Defibrillators Susan P. Etheridge, Shubhayan Sanatani, Mitchell I. Cohen, Cecilia A. Albaro, Elizabeth…”
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    Somatic mosaicism contributes to phenotypic variation in Timothy syndrome by Etheridge, Susan P., Bowles, Neil E., Arrington, Cammon B., Pilcher, Thomas, Rope, Alan, Wilde, Arthur A.M., Alders, Marielle, Saarel, Elizabeth V., Tavernier, Rene, Timothy, Katherine W., Tristani‐Firouzi, Martin

    “…Timothy syndrome type 1 (TS‐1) is a rare disorder that affects multiple organ systems and has a high incidence of sudden death due to profound QT prolongation…”
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    Implanted Defibrillators in Young Hypertrophic Cardiomyopathy Patients: A Multicenter Study by Kamp, Anna N., Von Bergen, Nicholas H., Henrikson, Charles A., Makhoul, Majd, Saarel, Elizabeth V., LaPage, Martin J., Russell, Mark W., Strieper, Margaret, Yu, Sunkyung, Dick, Macdonald, Day, Sharlene M., Bradley, David J.

    Published in Pediatric cardiology (01-10-2013)
    “…Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease, with an annual risk of sudden cardiac death (SCD) estimated at 1 %…”
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    A Teenage Fainter (Dizziness, Syncope, Postural Orthostatic Tachycardia Syndrome) by Pilcher, Thomas A., MD, MS, FHRS, Saarel, Elizabeth V., MD, FHRS

    Published in The Pediatric clinics of North America (01-02-2014)
    “…This article informs the general pediatrician about the diagnosis, evaluation, and treatment of teenage patients with presyncope and loss of consciousness. The…”
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    Waitlist and Post–Heart Transplant Outcomes for Children With Nondilated Cardiomyopathy by Amdani, Shahnawaz, Boyle, Gerard, Saarel, Elizabeth V., Godown, Justin, Liu, Wei, Worley, Sarah, Karamlou, Tara

    Published in The Annals of thoracic surgery (01-07-2021)
    “…Although outcomes for pediatric cardiomyopathy (CMP) patients have improved, an understanding of outcomes by CMP phenotype is essential. This study assessed…”
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    Failure to impact prevalence of arterial ischemic stroke in pediatric cardiac patients over three decades by Hoffman, James L, Mack, Gordon K, Minich, L LuAnn, Benedict, Susan L, Heywood, Mason, Stoddard, Gregory J, Saarel, Elizabeth V

    Published in Congenital heart disease (01-05-2011)
    “…Over the past three decades, significant advances in treatment have improved the mortality of children with cardiac disease. The effect of these advances on…”
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    Exercise participation and shared decision-making in patients with inherited channelopathies and cardiomyopathies by Etheridge, Susan P., Saarel, Elizabeth V., Martinez, Matthew W.

    Published in Heart rhythm (01-06-2018)
    “…Sports eligibility and disqualification of patients with cardiac diseases are important considerations for adult and pediatric cardiologists. The 2005…”
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