1. Aula, N., Jalanko, A., Aula, P., and Peltonen, L., 2002, Unraveling the molecular patho-genesis of free sialic acid storage disorders: altered targeting of mutant sialin, Mol Genet Metab 77: 99.
2. Aula, N., Kopra, O., Jalanko, A., and Peltonen, L., 2004, Sialin expression in the CNS implicates extralysosomal function in neurons, Neurobiol Dis 15: 251.
3. Aula, N., Salomaki, P., Timonen, R., Verheijen, F., Mancini, G., Mansson, J. E., Aula, P., and Peltonen, L., 2000, The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation, Am J Hum Genet 67: 832.
4. Aula, P., and Gahl, W., 2001, Disorders of Free Sialic Acid Storage. In The Metabolic and Molecular Bases of Inherited Disease, C. Scriver, A. Beaudet, W. Sly, and D. Valle, Eds. (New York, McGraw-Hill), pp. 5109-5120.
5. Aula, P., Autio, S., Raivio, K., Rapola, J., Thoden, C., Koskela, S., and Yamashina, I., 1979, “Salla Disease”. A new lysosomal storage disorder, Arch Neurol 36: 88.