Electrocardiographic response to enzyme replacement therapy for Pompe disease

Glycogen Storage Diseases Presenting as Hypertrophic Cardiomyopathy

Michael Arad, Barry J. Maron, Joshua Gorham et al. · New England Journal of Medicine · 2005 · 646 citations

Medicine, Cardiology, Pathology +14

Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial

Andrea Amalfitano, A. Resai Bengur, Richard P. Morse et al. · Genetics in Medicine · 2001 · 347 citations · Full text

Life Sciences, Biochemistry, Pediatrics +8

Transgenic Mice Overexpressing Mutant <i>PRKAG2</i> Define the Cause of Wolff-Parkinson-White Syndrome in Glycogen Storage Cardiomyopathy

Michael Arad, Ivan P. Moskowitz, Vickas V. Patel et al. · Circulation · 2003 · 320 citations · Full text

Medicine, Cardiology, Genetics +15

Targeted Disruption of the Acid α-Glucosidase Gene in Mice Causes an Illness with Critical Features of Both Infantile and Adult Human Glycogen Storage Disease Type II

Nina Raben, Kanneboyina Nagaraju, Eunice Lee et al. · Journal of Biological Chemistry · 1998 · 297 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Anatomic validation of left ventricular mass estimates from clinical two-dimensional echocardiography: initial results.

Nathaniel Reichek, J Helak, Theodore Plappert et al. · Circulation · 1983 · 277 citations

Medicine, Cardiology, Cardiothoracic Radiology +14