Professor, Medicine, Case Western Reserve University School of Medicine
Cardiology
Dr. Elizabeth S. Kaufman, MD
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Elizabeth Kaufman works in the field of Cardiology. She researched medicine at Harvard Medical School. Harvard Medical School is a top medical college. Harvard Medical School has a rank of 1 in research and a 12 in primary care She over the years received 7 awards: "Simon Dack Award for Outstanding Scholarship", "2008 publication selected", "Alpha Omega Alpha", "Aesculapian Club", "Hart Lyman Prize for academic excellence", "Phi Beta Kappa" and "Fellow (FACC)". Elizabeth Kaufman is also a published physician. She has 60 publication published. The most recent publication is: The Kv1.1 null mouse, a model of sudden unexpected death in epilepsy (SUDEP).
Publications
- The Kv1.1 null mouse, a model of sudden unexpected death in epilepsy (SUDEP).
- Prognostic implications of mutation-specific QTc standard deviation in congenital long QT Syndrome.
- Risk of life-threatening cardiac events among patients with long QT Syndrome and multiple mutations.
- T-wave window adjustment for determination of microvolt T-wave alternans (response to letter to the editor).
- Microvolt-level T-wave alternans determination using the spectral method in patients with QT prolongation: value of adjusting the T-wave window.
- J Mutation Location Matters in Long QT Syndrome Type 2 (But Behavior Matters More).
- Positive predictive value of device-detected Atrial high-rate episodes at different rates and durations: An analysis from ASSERT.
- Genetic Testing in Brugada Syndrome.
- HASH(0xb9473f0)
- Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to beta-blocker therapy in typ...
- Subclinical Atrial fibrillation and the risk of stroke.
- Breakdown of the Integration Center: Right Atrial Ganglionated Plexus Dysfunction in Heart Failure.
- Arrhythmic risk in congenital long QT Syndrome.
- Trigger-Specific Ion-channel Mechanisms, Risk Factors, and Response to Therapy in Type 1 Long QT Syndrome.
- Risk of Syncope in Family Members Who Are Genotype Negative for a Family-Associated Long QT Syndrome Mutation.
- Clinical Cardiac Electrophysiology Fellowship Curriculum: Update 2011.
- β-blockers protect against dispersion of repolarization during exercise in congenital long-QT Syndrome type 1.
- Risk of Recurrent Cardiac Events After Onset of Menopause in Women With Congenital Long-QT Syndrome Types 1 and 2.
- Mutation and Gender Specific Risk in Type-2 Long QT Syndrome: Implications for Risk Stratification for Life-Threatening Cardiac Events in Patients with Long QT Syndrome.
- Genotype-Specific QT Correction for Heart Rate and the Risk of Life Threatening Cardiac Events in Adolescents with the Congenital Long-QT Syndrome.
- A common SCN5A polymorphism modulates the biophysical Defects of SCN5A mutations.
- Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT Syndrome and normal-range corrected QT intervals.
- Trigger-specific risk factors and response to therapy in long QT Syndrome type 2.
- Letter by Kaufman regarding article, "Closer look at genetic testing in long-QT Syndrome: will DNA diagnostics ever be enough?".
- To the editor-a small epidemic of "frozen" pacemaker and defibrillator leads.
- Genotype-phenotype aspects of type 2 long QT Syndrome.
- Disease-causing polymorphisms in the spectrum of long QT Syndrome mutations.
- Clinical implications for patients with long QT Syndrome who experience a cardiac event during infancy.
- Mechanisms and clinical management of inherited channelopathies: long QT Syndrome, Brugada Syndrome, catecholaminergic polymorphic ventricular tachycardia, and short Q...
- Microvolt T-wave alternans, peak oxygen consumption, and outcome in patients with severely impaired left ventricular systolic function.
- Use of ranolazine in long-QT Syndrome type 3.
- A surprise wireless remote transmission.
- Risk of death in the long QT Syndrome when a sibling has died.
- Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT Syndrome.
- Long-QT Syndrome after age 40.
- I(Kr) channel blockade to unmask occult congenital long QT Syndrome.
- Quinidine in short QT Syndrome: an old drug for a new disease.
- Clinical aspects of type-1 long-QT Syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene.
- Long QT Syndrome and pregnancy.
- Long QT Syndrome in adults.
- "Indeterminate" microvolt T-wave alternans tests predict high risk of death or sustained ventricular Arrhythmias in patients with left ventricular dysfunction.
- Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT Syndrome.
- Arrhythmogenic right ventricular Cardiomyopathy: how should genetic information be integrated with clinical diagnostic criteria?
- Microvolt T-wave alternans and the risk of death or sustained ventricular Arrhythmias in patients with left ventricular dysfunction.
- Efficient genotyping for congenital long QT Syndrome.
- Use of autonomic maneuvers to probe phenotype/genotype discordance in congenital long QT Syndrome.
- Evaluation of suspected arrhythmic Syncope: leaning away from tilting.
- Can common genetic variations combine to produce the long QT Syndrome phenotype?
- How to find the high-risk patient among individuals with a Brugada Syndrome-type electrocardiogram.
- Microvolt T-wave alternans distinguishes between patients likely and patients not likely to benefit from implanted cardiac defibrillator therapy: a solution to the Mul...
- The impact of asymptomatic Atrial fibrillation.
- Saving lives in congenital long QT Syndrome: who benefits from implantable cardioverter defibrillator therapy?
- Is restoration of intracellular trafficking clinically feasible in the long QT Syndrome?: The example of HERG mutations.
- Autonomic alterations in cocaine-exposed infants.
- Heart rate variability by triangular index in infants exposed prenatally to cocaine.
- Repolarization dynamics in patients with long QT Syndrome.
- Increased risk of arrhythmic events in long-QT Syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
- Variable expression of long QT Syndrome among gene carriers from families with five different HERG mutations.
- Heart rate variability in healthy newborn infants.
Schools
Harvard Medical School
Colum Presby Med Center
Ny and Presby Hp Columbia Campus
Procedures Preformed
- Ablation for Treatment of Cardiac Arrhythmias
- Automatic Implantable Cardioverter Defibrillator (ICD) Implantation
- Cardiac Catheterization (incl. Coronary Angiography)
- Cardiac Imaging
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Conditions Treated
- Aneurysm and Dissection of Heart
- Angina and Acute Coronary Syndrome
- Aortic Aneurysm
- Aortic Valve Disease
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Doctors Specialties
- Cardiology
- Clinical Cardiac Electrophysiology
Accepted Insurances
Awards
- Simon Dack Award for Outstanding Scholarship
- 2008 publication selected
- Alpha Omega Alpha
- Aesculapian Club
- Hart Lyman Prize for academic excellence
- Phi Beta Kappa
- Fellow (FACC)
Education
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New York Presbyterian Hospital - Columbia Campus -
Harvard Medical School -
Yale University
Hospital
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MetroHealth Medical Center
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