| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2000 | Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders | Shen, J. J.; Matern, D.; Millington, D. S.; Hillman, S.; Feezor, M. D.; Bennett, M. J.; Qumsiyeh, M.; Kahler, S. G.; Chen, Y. T.; Van Hove, J. L. | J Inherit Metab Dis 23, 27-44 | | | |
| 2000 | Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype | Weston, B. W.; Lin, J. L.; Muenzer, J.; Cameron, H. S.; Arnold, R. R.; Seydewitz, H. H.; Mayatepek, E.; Van Schaftingen, E.; Veiga-da-Cunha, M.; Matern, D.; Chen, Y. T. | Pediatr Res 48, 329-334 | | | |
| 2002 | Glycogen storage disease type I: diagnosis and phenotype/genotype correlation | Matern, D.; Seydewitz, H. H.; Bali, D.; Lang, C.; Chen, Y. T. | Eur J Pediatr 161, S10-S19 | | | |
| 1999 | Liver transplantation for glycogen storage disease types I, III, and IV | Matern, D.; Starzl, T. E.; Arnaout, W.; Barnard, J.; Bynon, J. S.; Dhawan, A.; Emond, J.; Haagsma, E. B.; Hug, G.; Lachaux, A.; Smit, G. P.; Chen, Y. T. | Eur J Pediatr 158, S43-S48 | | | |
| 2002 | Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex | Chou, J. Y.; Matern, D.; Mansfield, B. C.; Chen, Y. T. | Curr Mol Med 2, 121-143 | | | |
