Michael J. Campbell, MD

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Assistant Professor of Pediatrics
Department / Division:
Pediatrics / Pediatrics-Cardiology
Address:
DUMC 3090
Durham, NC 27710

1236 Huffman Mill Road
Medical Arts Building, Suite 1600
Burlington, NC 27215

23 Sunnybrook Road, Suite 200
Raleigh, NC 27610
Appointment Telephone:
919-668-4000, 336-586-3553
Office Telephone:
919-684-3574
Fax:
919-681-5903, 336-586-3588
Training:
  • MD, University of South Carolina School of Medicine, 2001
Residency:
  • Pediatrics, Vanderbilt University Medical Center (Tennessee), 2001-2004
Fellowship:
  • Pediatric Cardiology, Vanderbilt University Medical Center (Tennessee), 2004-2007
  • Cardiovascular Pharmacology, Vanderbilt University Medical Center (Tennessee), 2006-2007
  • Advanced Cardiac Imaging, Vanderbilt University Medical Center (Tennessee), 2007-2008
Clinical Interests:
Children and adults with congenital heart disease, transesophageal echocardiography, fetal echocardiography, cardiac MRI
Research Interests:
Clinical interests include pediatric echocardiography, fetal echocardiography, pediatric/congenital cardiac MRI, treatment of children with acquired and congenital heart disease.

Educational interests include the education of pediatric cardiology fellows, pediatric residents and medical students in pediatric cardiology.

Research interests include cardiac imaging research (echocardiography and cardiac MRI) in children and adults with congenital heart disease. Clinical research interests also include fetal echocardiography. Basic science research interests include the genetics of congenital and acquired aortic stenosis.
Representative Publications:
  • Hornik, CP; Campbell, MJ; Carboni, MP; Lodge, AJ; Rhodes, JF; Kanter, RJ. Preoperative diagnosis of long QT syndrome in an infant with tetralogy of Fallot. Pediatric Cardiology. 2011;32:834-838.  Abstract
  • Barker, PC; Pasquali, SK; Darty, S; Ing, RJ; Li, JS; Kim, RJ; DeArmey, S; Kishnani, PS; Campbell, MJ. Use of cardiac magnetic resonance imaging to evaluate cardiac structure, function and fibrosis in children with infantile Pompe disease on enzyme replacement therapy. Molecular Genetics and Metabolism. 2010;101:332-337.  Abstract
  • Todd, SJ; Campbell, MJ; Roden, DM; Kannankeril, PJ. Novel Brugada SCN5A mutation causing sudden death in children. Heart Rhythm. 2005;2:540-543.  Abstract