| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2006 | Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease | Kishnani, P. S.; Nicolino, M.; Voit, T.; Rogers, R. C.; Tsai, A. C.; Waterson, J.; Herman, G. E.; Amalfitano, A.; Thurberg, B. L.; Richards, S.; Davison, M.; Corzo, D.; Chen, Y. T. | J Pediatr 149(1), 89-97 | | | |
| 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 | | | |
| 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 | | | |
| 2007 | Recombinant human acid alpha-glucosidase. Major clinical benefits in infantile-onset Pompe disease | Kishnani, P. S.; Corzo, D.; Nicolino, M.; Byrne, B.; Mandel, H.; Hwu, W. L.; Leslie, N.; Levine, J.; Spencer, C.; McDonald, M.; Li, J.; Dumontier, J.; Halberthal, M.; Chien, Y. H.; Hopkin, R.; Vijayaraghavan, S.; Gruskin, D.; Bartholomew, D.; van der Ploeg, A.; Clancy, J. P.; Parini, R.; Morin, G.; Beck, M.; De la Gastine, G. S.; Jokic, M.; Thurberg, B.; Richards, S.; Bali, D.; Davison, M.; Worden, M. A.; Chen, Y. T.; Wraith, J. E. | Neurology 68(2), 99-109 | | | |
| 2007 | Sibling phenotype concordance in classical infantile Pompe disease | Smith, W. E.; Sullivan-Saarela, J. A.; Li, J. S.; Cox, G. F.; Corzo, D.; Chen, Y. T.; Kishnani, P. S. | Am J Med Genet A 143A(21), 2493-501 | | | |
