Michael Jay Campbell

Journal article Pediatr Cardiol · August 2011 Featured Publication Long QT syndrome is a well-described entity in infants. Its presentation in the context of congenital heart disease is rare and is almost exclusively diagnosed postoperatively. For patients undergoing surgical intervention, preoperative knowledge of the di ... Full text Link to item Cite

Use of cardiac magnetic resonance imaging to evaluate cardiac structure, function and fibrosis in children with infantile Pompe disease on enzyme replacement therapy.

Journal article Mol Genet Metab · December 2010 Featured Publication BACKGROUND: Pompe disease (acid α-glucosidase deficiency) is one of several lysosomal storage diseases amenable to treatment with enzyme replacement therapy (ERT). While echocardiography (echo) has been the standard method to evaluate the cardiac response ... Full text Link to item Cite

Novel Brugada SCN5A mutation causing sudden death in children.

Journal article Heart Rhythm · May 2005 Featured Publication Full text Link to item Cite