| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 1992 | Genetic heterogeneity in MCAD deficiency: frequency of K329E allele and identification of three additional mutant alleles | Ding, J. -H.; Bross, P.; Yang, B. -Z.; Iafolla, A. K.; Millington, D. S.; Roe, C. R.; Gregersen, N.; Chen, Y. -T. | New Developments in fatty acid oxidation (New York : Wiley-Liss) | | | |
| 1992 | Isolating Metabolic causes of the sudden infant death syndrome | Iafolla, A. K.; Chen, Y. T. | J Respir Dis 12, 1102-1104 | | | |
| 1992 | Low plasma citrulline concentrations during protein restriction in an unaffected infant at risk for ornithine transcarbamylase deficiency | Iafolla, A. K.; Kahler, S. G.; Chen, Y. T. | J Pediatr 120, 496-497 | | | |
| 1993 | Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood | Van Hove, J. L.; Zhang, W.; Kahler, S. G.; Roe, C. R.; Chen, Y. T.; Terada, N.; Chace, D. H.; Iafolla, A. K.; Ding, J. H.; Millington, D. S. | Am J Hum Genet 52, 958-966 | | | |
| 1991 | Medium-chain acyl-coenzyme A dehydrogenase deficiency and sudden infant death | Ding, J. H.; Roe, C. R.; Iafolla, A. K.; Chen, Y. T. | N Engl J Med 325, 61-62 | | | |
| 1992 | Unbalanced translocation 46,XY,-15,+der(22)t(1522)(q13q11)pat: case report and review of the literature | Van Hove, J. L.; McConkie-Rosell, A.; Chen, Y. T.; Iafolla, A. K.; Lanman Jr., J. T.; Hennessy, M. D.; Kahler, S. G. | Am J Med Genet 44, 24-30 | | | |
| 1991 | VATER and hydrocephalus: distinct syndrome? | Iafolla, A. K.; McConkie-Rosell, A.; Chen, Y. T. | Am J Med Genet 38, 46-51 | | | |
