| 2004 | Nephrotic syndrome complicating alpha-glucosidase replacement therapy for Pompe disease | Hunley, T. E.; Corzo, D.; Dudek, M.; Kishnani, P.; Amalfitano, A.; Chen, Y. T.; Richards, S. M.; Phillips, J. A.; Fogo, A. B.; Tiller, G. E. | Pediatrics 114, e532-e535 | | | |
| 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 | | | |
