| 2007 | Fractures in children with Pompe disease: a potentiallong-term complication | Case, L. E.; Hanna, R.; Frush, D. P.; Krishnamurthy, V.; DeArmey, S.; Mackey, J.; Boney, A.; Morgan, C.; Corzo, D.; Bouchard, S.; Weber, T. J.; Chen, Y. T.; Kishnani, P. S. | Pediatr Radiol 37(5), 437-445 | | | |
| 2001 | Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trial | Amalfitano, A.; Bengur, A. R.; Morse, R. P.; Majure, J. M.; Case, L. E.; Veerling, D. L.; Mackey, J.; Kishnani, P.; Smith, W.; McVie-Wylie, A.; Sullivan, J. A.; Hoganson, G. E.; Phillips, J. A.; Schaefer, G. B.; Charrow, J.; Ware, R. E.; Bossen, E. H.; Chen, Y. T. | Genet Med 3, 132-138 | | | |
