Michael John Ackerman, MD, PhD, FACC

  • 35048 Citations
  • 103 Scopus h-Index
1991 …2020
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Research Output 1991 2019

2009
17 Citations (Scopus)

Long QT syndrome due to a novel mutation in SCN5A: Treatment with ICD placement at 1 month and left cardiac sympathetic denervation at 3 months of age

Silver, E. S., Liberman, L., Chung, W. K., Spotnitz, H. M., Chen, J. M., Ackerman, M. J., Moir, C., Hordof, A. J. & Pass, R. H., Oct 2009, In : Journal of Interventional Cardiac Electrophysiology. 26, 1, p. 41-45 5 p.

Research output: Contribution to journalArticle

Torsades de Pointes
Long QT Syndrome
Sympathectomy
Mutation
Newborn Infant
49 Citations (Scopus)

Molecular evolution of the junctophilin gene family

Garbino, A., Van Oort, R. J., Dixit, S. S., Landstrom, A. P., Ackerman, M. J. & Wehrens, X. H. T., May 2009, In : Physiological Genomics. 37, 3, p. 175-186 12 p.

Research output: Contribution to journalArticle

Molecular Evolution
Genes
Calcium Channels
Membranes
Protein Isoforms
30 Citations (Scopus)

Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndrome

Jons, C., Moss, A. J., Lopes, C. M., McNitt, S., Zareba, W., Goldenberg, I., Qi, M., Wilde, A. A. M., Shimizu, W., Kanters, J. K., Towbin, J. A., Ackerman, M. J. & Robinson, J. L., Aug 2009, In : Journal of Cardiovascular Electrophysiology. 20, 8, p. 859-865 7 p.

Research output: Contribution to journalArticle

Romano-Ward Syndrome
Amino Acids
Mutation
Heart Arrest
Voltage-Gated Potassium Channels
17 Citations (Scopus)
Hypertrophic Cardiomyopathy
Left Ventricular Hypertrophy
Renin-Angiotensin System
Fibrosis
Genotype
76 Citations (Scopus)

Outcome of Patients With Hypertrophic Cardiomyopathy and a Normal Electrocardiogram

McLeod, C. J., Ackerman, M. J., Nishimura, R. A., Tajik, A. J., Gersh, B. J. & Ommen, S. R., Jul 14 2009, In : Journal of the American College of Cardiology. 54, 3, p. 229-233 5 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Electrocardiography
Phenotype
Implantable Defibrillators
Sudden Death
43 Citations (Scopus)

Protein kinase a-Dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardia

Makielski, J. C., Vega, A. L., Tester, D. J. & Ackerman, M. J., Oct 2009, In : Circulation: Arrhythmia and Electrophysiology. 2, 5, p. 540-547 8 p.

Research output: Contribution to journalArticle

Cyclic AMP-Dependent Protein Kinases
Protein Kinases
Andersen Syndrome
Phenotype
Mutation
114 Citations (Scopus)

QTc: How long is too long?

Johnson, J. N. & Ackerman, M. J., Sep 2009, In : British Journal of Sports Medicine. 43, 9, p. 657-662 6 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Torsades de Pointes
Syncope
Genetic Testing
Sudden Death
13 Citations (Scopus)

QT interval variability and adaptation to heart rate changes in patients with long QT syndrome

Němec, J., Buncová, M., Shusterman, V., Winter, B., Shen, W. K. & Ackerman, M. J., Jan 2009, In : PACE - Pacing and Clinical Electrophysiology. 32, 1, p. 72-81 10 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Heart Rate
Linear Models
Nonlinear Dynamics
Cardiac Arrhythmias

Response to Elliott and McKenna

Maron, B. J., Seidman, C. E., Ackerman, M. J., Towbin, J. A., Maron, M. S., Ommen, S. R., Nishimura, R. A. & Gersh, B. J., Feb 2009, In : Circulation: Cardiovascular Genetics. 2, 1, p. 89 1 p.

Research output: Contribution to journalArticle

Response to letter regarding article, prevalence, clinical significance, and natural history of left ventricular apical aneurysms in hypertrophic cardiomyopathy

Maron, M. S., Finley, J. J., Udelson, J. E., Bos, J. M., Ackerman, M. J., Hauser, T. H., Manning, W. J., Haas, T. S., Lesser, J. R. & Maron, B. J., Jun 9 2009, In : Circulation. 119, 22

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Natural History
Aneurysm
83 Citations (Scopus)

Sodium channel mutation in irritable bowel syndrome: Evidence for an ion channelopathy

Saito Loftus, Y. A., Strege, P. R., Tester, D. J., Locke, G. R., Talley, N. J., Bernard, C. E., Rae, J. L., Makielski, J. C., Ackerman, M. J. & Farrugia, G., Feb 2009, In : American Journal of Physiology - Gastrointestinal and Liver Physiology. 296, 2

Research output: Contribution to journalArticle

Channelopathies
Sodium Channels
Irritable Bowel Syndrome
Ions
Mutation
245 Citations (Scopus)

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test

Kapplinger, J. D., Tester, D. J., Salisbury, B. A., Carr, J. L., Harris-Kerr, C., Pollevick, G. D., Wilde, A. A. M. & Ackerman, M. J., 2009, In : Heart Rhythm. 6, 9, p. 1297-1303 7 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Mutation
Channelopathies
Genes
Genetic Testing
46 Citations (Scopus)
Sudden Infant Death
Sudden Cardiac Death
Genetic Testing
Sudden Death
Autopsy
1 Citation (Scopus)

Subacute perforation of the st. jude riata implantable cardioverter- defibrillator lead: A report of two pediatric cases

Morrison, T. B., Ackerman, M. J. & Rea, R. F., Aug 2009, In : Pediatric Cardiology. 30, 6, p. 834-836 3 p.

Research output: Contribution to journalArticle

Implantable Defibrillators
Pediatrics
Lead
31 Citations (Scopus)

Sudden infant death syndrome: Do ion channels play a role?

Van Norstrand, D. W. & Ackerman, M. J., Feb 2009, In : Heart Rhythm. 6, 2, p. 272-278 7 p.

Research output: Contribution to journalArticle

Channelopathies
Long QT Syndrome
Mass Screening
Sudden Infant Death
Ion Channels
185 Citations (Scopus)

The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome. A Comprehensive Open Reading Frame Mutational Analysis

Medeiros-Domingo, A., Bhuiyan, Z. A., Tester, D. J., Hofman, N., Bikker, H., van Tintelen, J. P., Mannens, M. M. A. M., Wilde, A. A. M. & Ackerman, M. J., Nov 24 2009, In : Journal of the American College of Cardiology. 54, 22, p. 2065-2074 10 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Ryanodine Receptor Calcium Release Channel
Open Reading Frames
Genotype
Exercise
13 Citations (Scopus)

Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A

Medeiros-Domingo, A., Tan, B. H., Iturralde-Torres, P., Tester, D. J., Tusié-Luna, T., Makielski, J. C. & Ackerman, M. J., Aug 2009, In : Heart Rhythm. 6, 8, p. 1170-1175 6 p.

Research output: Contribution to journalArticle

Phenotype
Mutation
Fever
Ventricular Tachycardia
Romano-Ward Syndrome
42 Citations (Scopus)

What's in a name? Dilemmas in nomenclature characterizing hypertrophic cardiomyopathy and left ventricular hypertrophy

Maron, B. J., Seidman, C. E., Ackerman, M. J., Towbin, J. A., Maron, M. S., Ommen, S. R., Nishimura, R. A. & Gersh, B. J., Feb 2009, In : Circulation: Cardiovascular Genetics. 2, 1, p. 81-85 5 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Left Ventricular Hypertrophy
Terminology
Names
63 Citations (Scopus)

α1-Syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current

Ackerman, M. J., Cheng, J., Van Norstrand, D. W., Medeiros-Domingo, A., Valdivia, C., Tan, B. H., Ye, B., Kroboth, S., Vatta, M., Tester, D. J., January, C. T. & Makielski, J. C., Dec 2009, In : Circulation: Arrhythmia and Electrophysiology. 2, 6, p. 667-676 10 p.

Research output: Contribution to journalArticle

Sudden Infant Death
Sodium
Nitric Oxide Synthase Type I
Mutation
Long QT Syndrome
2008
92 Citations (Scopus)

alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption.

Wu, G., Ai, T., Kim, J. J., Mohapatra, B., Xi, Y., Li, Z., Abbasi, S., Purevjav, E., Samani, K., Ackerman, M. J., Qi, M., Moss, A. J., Shimizu, W., Towbin, J. A., Cheng, J. & Vatta, M., Aug 2008, In : Circulation. Arrhythmia and electrophysiology. 1, 3, p. 193-201 9 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Sodium Channels
Mutation
HEK293 Cells
Cardiac Myocytes
47 Citations (Scopus)

A mutation in telethonin alters Nav1.5 function

Mazzone, A., Strege, P. R., Tester, D. J., Bernard, C. E., Faulkner, G., De Giorgio, R., Makielski, J. C., Stanghellini, V., Gibbons, S. J., Ackerman, M. J. & Farrugia, G., Jun 13 2008, In : Journal of Biological Chemistry. 283, 24, p. 16537-16544 8 p.

Research output: Contribution to journalArticle

Intestinal Pseudo-Obstruction
Mutation
Sodium Channels
Ion Channels
Romano-Ward Syndrome

A mutation in telethonin alters Nav1.5 function (Journal of Biological Chemistry (2008) 283 (16537-16544))

Mazzone, A., Strege, P. R., Tester, D. J., Bernard, C. E., Faulkner, G., De Giorgio, R., Makielski, J. C., Stanghellini, V., Gibbons, S. J., Ackerman, M. J. & Farrugia, G., Aug 8 2008, In : Journal of Biological Chemistry. 283, 32, p. 22336 1 p.

Research output: Contribution to journalArticle

Mutation
3 Citations (Scopus)

Arrhythmogenic malignancies in hypertrophic cardiomyopathy

Menon, S. C., Bos, J. M., Ommen, S. R. & Ackerman, M. J., 2008, Electrical Diseases of the Heart: Genetics, Mechanisms, Treatment, Prevention. Springer London, p. 610-626 17 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Hypertrophic Cardiomyopathy
Cardiomyopathies
Neoplasms
Restrictive Cardiomyopathy
Arrhythmogenic Right Ventricular Dysplasia
18 Citations (Scopus)

A splice site mutation in hERG leads to cryptic splicing in human long QT syndrome

Gong, Q., Zhang, L., Moss, A. J., Vincent, G. M., Ackerman, M. J., Robinson, J. C., Jones, M. A., Tester, D. J. & Zhou, Z., Mar 2008, In : Journal of Molecular and Cellular Cardiology. 44, 3, p. 502-509 8 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Ether
RNA Splice Sites
Mutation
Introns
10 Citations (Scopus)

Congenital long QT syndrome

Ackerman, M. J., Khositseth, A., Tester, D. J. & Schwartz, P. J., 2008, Electrical Diseases of the Heart: Genetics, Mechanisms, Treatment, Prevention. Springer London, p. 462-482 21 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Long QT Syndrome
Cardiac Arrhythmias
Channelopathies
Bryophyta
Acoustic Stimulation
54 Citations (Scopus)

Depletion of zebrafish essential and regulatory myosin light chains reduces cardiac function through distinct mechanisms

Chen, Z., Huang, W., Dahme, T., Rottbauer, W., Ackerman, M. J. & Xu, X. H., Jul 2008, In : Cardiovascular Research. 79, 1, p. 97-108 12 p.

Research output: Contribution to journalArticle

Myosin Light Chains
Zebrafish
Morpholinos
Sarcomeres
Cardiac Myocytes
12 Citations (Scopus)

Electrical diseases of the heart: Genetics, mechanisms, treatment, prevention

Gussak, I., Antzelevitch, C., Wilde, A. A. M., Friedman, P. A., Ackerman, M. J. & Shen, W. K., 2008, Springer London. 968 p.

Research output: Book/ReportBook

Inborn Genetic Diseases
Heart Diseases
Cardiac Electrophysiology
Distillation
Pharmacology
8 Citations (Scopus)

Genetic testing

Tester, D. J. & Ackerman, M. J., 2008, Electrical Diseases of the Heart: Genetics, Mechanisms, Treatment, Prevention. Springer London, p. 444-458 15 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Genetic Testing
Molecular Medicine
Inborn Genetic Diseases
Research
25 Citations (Scopus)

Impact of Septal Myectomy on Left Atrial Volume and Left Ventricular Diastolic Filling Patterns: An Echocardiographic Study of Young Patients with Obstructive Hypertrophic Cardiomyopathy

Menon, S. C., Ackerman, M. J., Ommen, S. R., Cabalka, A. K., Hagler, D. J., O'Leary, P. W., Dearani, J. A., Cetta, F. & Eidem, B. W., Jun 2008, In : Journal of the American Society of Echocardiography. 21, 6, p. 684-688 5 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Mitral Valve Insufficiency
Hemodynamics
Ventricular Outflow Obstruction
Exercise Tolerance
109 Citations (Scopus)

Long-QT syndrome after age 40

Goldenberg, I., Moss, A. J., Peterson, D. R., McNitt, S., Zareba, W., Andrews, M. L., Robinson, J. L., Locati, E. H., Ackerman, M. J., Benhorin, J., Kaufman, E. S., Napolitano, C., Priori, S. G., Qi, M., Schwartz, P. J., Towbin, J. A., Vincent, G. M. & Zhang, L., Apr 29 2008, In : Circulation. 117, 17, p. 2192-2201 10 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Heart Arrest
Genotype
Age Factors
Syncope
14 Citations (Scopus)

Mechanical Dysfunction in Extreme QT Prolongation

Vyas, H., O'Leary, P. W., Earing, M. G., Cetta, F. & Ackerman, M. J., May 2008, In : Journal of the American Society of Echocardiography. 21, 5

Research output: Contribution to journalArticle

Long QT Syndrome
Torsades de Pointes
Atrioventricular Block
Bradycardia
DNA Sequence Analysis
74 Citations (Scopus)

Molecular and functional characterization of novel hypertrophic cardiomyopathy susceptibility mutations in TNNC1-encoded troponin C

Landstrom, A. P., Parvatiyar, M. S., Pinto, J. R., Marquardt, M. L., Bos, J. M., Tester, D. J., Ommen, S. R., Potter, J. D. & Ackerman, M. J., Aug 2008, In : Journal of Molecular and Cellular Cardiology. 45, 2, p. 281-288 8 p.

Research output: Contribution to journalArticle

Troponin C
Hypertrophic Cardiomyopathy
Mutation
Genes
Tropomyosin
252 Citations (Scopus)

Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy

Olivotto, I., Girolami, F., Ackerman, M. J., Nistri, S., Bos, J. M., Zachara, E., Ommen, S. R., Theis, J. L., Vaubel, R. A., Re, F., Armentano, C., Poggesi, C., Torricelli, F. & Cecchi, F., 2008, In : Mayo Clinic Proceedings. 83, 6, p. 630-638 9 p.

Research output: Contribution to journalArticle

Myofibrils
Hypertrophic Cardiomyopathy
Mutation
Proteins
Sarcomeres
16 Citations (Scopus)

Novel gene and mutation discovery in congenital long QT syndrome: Let's keep looking where the street lamp standeth

Tester, D. J. & Ackerman, M. J., Sep 2008, In : Heart Rhythm. 5, 9, p. 1282-1284 3 p.

Research output: Contribution to journalArticle

Ether-A-Go-Go Potassium Channels
KCNQ1 Potassium Channel
Long QT Syndrome
Gene Deletion
Genetic Association Studies
47 Citations (Scopus)
Sudden Infant Death
Sodium Channels
Sudden Death
African Americans
Population
84 Citations (Scopus)

Physiological properties of hERG 1a/1b heteromeric currents and a hERG 1b-specific mutation associated with long-QT syndrome

Sale, H., Wang, J., O'Hara, T. J., Tester, D. J., Phartiyal, P., He, J. Q., Rudy, Y., Ackerman, M. J. & Robertson, G. A., Sep 26 2008, In : Circulation Research. 103, 7

Research output: Contribution to journalArticle

Long QT Syndrome
HEK293 Cells
Mutation
Missense Mutation
Pharmaceutical Preparations
70 Citations (Scopus)
Genetic Testing
Sudden Death
Paraffin
Autopsy
DNA
290 Citations (Scopus)

Prevalence, clinical significance, and natural history of left ventricular apical aneurysms in hypertrophic cardiomyopathy

Maron, M. S., Finley, J. J., Bos, J. M., Hauser, T. H., Manning, W. J., Haas, T. S., Lesser, J. R., Udelson, J. E., Ackerman, M. J. & Maron, B. J., Oct 7 2008, In : Circulation. 118, 15, p. 1541-1549 9 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Natural History
Aneurysm
Magnetic Resonance Spectroscopy
Echocardiography
111 Citations (Scopus)

Prevalence of early-onset atrial fibrillation in congenital long QT syndrome

Johnson, J. N., Tester, D. J., Perry, J., Salisbury, B. A., Reed, C. R. & Ackerman, M. J., May 2008, In : Heart Rhythm. 5, 5, p. 704-709 6 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Atrial Fibrillation
Kv1.5 Potassium Channel
Mutation
Andersen Syndrome
2 Citations (Scopus)

Provocative testing in inherited arrhythmias

Shimizu, W. & Ackerman, M. J., 2008, Electrical Diseases of the Heart: Genetics, Mechanisms, Treatment, Prevention. Springer London, p. 424-433 10 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Brugada Syndrome
Long QT Syndrome
Cardiac Arrhythmias
Tachycardia
Channelopathies
15 Citations (Scopus)

Relationship between sex, shape, and substrate in hypertrophic cardiomyopathy

Bos, J. M., Theis, J. L., Tajik, A. J., Gersh, B. J., Ommen, S. R. & Ackerman, M. J., Jun 2008, In : American Heart Journal. 155, 6, p. 1128-1134 7 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Sex Characteristics
Ventricular Outflow Obstruction
Sarcomeres
Phenotype
200 Citations (Scopus)

Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital Long-QT syndrome

Goldenberg, I., Moss, A. J., Peterson, D. R., McNitt, S., Zareba, W., Andrews, M. L., Robinson, J. L., Locati, E. H., Ackerman, M. J., Benhorin, J., Kaufman, E. S., Napolitano, C., Priori, S. G., Qi, M., Schwartz, P. J., Towbin, J. A., Vincent, G. M. & Zhang, L., Apr 29 2008, In : Circulation. 117, 17, p. 2184-2191 8 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Sudden Cardiac Death
Syncope
Heart Arrest
Confidence Intervals
55 Citations (Scopus)

Risk of death in the long QT syndrome when a sibling has died

Kaufman, E. S., McNitt, S., Moss, A. J., Zareba, W., Robinson, J. L., Hall, W. J., Ackerman, M. J., Benhorin, J., Locati, E. T., Napolitano, C., Priori, S. G., Schwartz, P. J., Towbin, J. A., Vincent, G. M. & Zhang, L., Jun 2008, In : Heart Rhythm. 5, 6, p. 831-836 6 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Siblings
Syncope
Heart Arrest
Sudden Death
28 Citations (Scopus)

Significance of Left Atrial Volume in Patients < 20 Years of Age With Hypertrophic Cardiomyopathy

Menon, S. C., Ackerman, M. J., Cetta, F., O'Leary, P. W. & Eidem, B. W., Nov 15 2008, In : American Journal of Cardiology. 102, 10, p. 1390-1393 4 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Mitral Valve Insufficiency
Exercise
Pediatrics
Exercise Test
1 Citation (Scopus)

Sudden cardiac death in infancy: Focus on prolonged repolarization

Schwartz, P. J., Stramba-Badiale, M., Crotti, L. & Ackerman, M. J., 2008, Electrical Diseases of the Heart: Genetics, Mechanisms, Treatment, Prevention. Springer London, p. 924-933 10 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Sudden Cardiac Death
Western World
Sudden Infant Death
Sudden Death
Cause of Death

Sudden infant death syndrome: Study of genes pertinent to cardiorespiratory and autonomic regulation

Weese-Mayer, D. E., Ackerman, M. J., Marazita, M. L. & Berry-Kravis, E. M., 2008, Genetic Basis for Respiratory Control Disorders. Springer US, p. 85-109 25 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Sudden Infant Death
death
risk factors
Genes
genes

Sudden infant death syndrome: Genetic studies in cardiorespiratory and autonomic regulation

Weese-Mayer, D. E., Berry-Kravis, E. M., Ackerman, M. J. & Marazita, M. L., Jan 1 2008, Sleep and Breathing in Children: Developmental Changes in Breathing During Sleep, Second Edition. CRC Press, Vol. 224. p. 224-313 90 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Sudden Infant Death
Live Birth
Genetic Association Studies
African Americans
Sleep
11 Citations (Scopus)

Suppression of atrial fibrillation with mexiletine pharmacotherapy in a young woman with type 1 long QT syndrome

El Yaman, M., Perry, J., Makielski, J. C. & Ackerman, M. J., Mar 2008, In : Heart Rhythm. 5, 3, p. 472-474 3 p.

Research output: Contribution to journalArticle

Romano-Ward Syndrome
Mexiletine
Long QT Syndrome
Anti-Arrhythmia Agents
Atrial Fibrillation
248 Citations (Scopus)

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

Ueda, K., Valdivia, C., Medeiros-Domingo, A., Tester, D. J., Vatta, M., Farrugia, G., Ackerman, M. J. & Makielski, J. C., Jul 8 2008, In : Proceedings of the National Academy of Sciences of the United States of America. 105, 27, p. 9355-9360 6 p.

Research output: Contribution to journalArticle

Macromolecular Substances
Long QT Syndrome
Nitric Oxide Synthase Type I
Adenosine Triphosphatases
Mutation
51 Citations (Scopus)

Systems approach to understanding electromechanical activity in the human heart a national heart, lung, and blood institute workshop summary

Rudy, Y., Ackerman, M. J., Bers, D. M., Clancy, C. E., Houser, S. R., London, B., McCulloch, A. D., Przywara, D. A., Rasmusson, R. L., Solaro, J. R., Trayanova, N. A., Van Wagoner, D. R., Varro, A., Weiss, J. N. & Lathrop, D. A., Sep 9 2008, In : Circulation. 118, 11, p. 1202-1211 10 p.

Research output: Contribution to journalArticle

National Heart, Lung, and Blood Institute (U.S.)
Systems Analysis
Human Activities
Education
Electrophysiology