1. Anderson, E. P., Kalckar, H. M., Isselbacher, K.J.: Defect in uptake of galactose-1-phosphate into liver nucleotides in congenital galactosemia. Science 125, 113–114 (1959).
2. Anderson, E. P., Kalckar, H. M., Kurahashi, K., Isselbacher, K. J.: A specific enzymatic assay for the diagnosis of congenital galactosemia. I. The comsumption test. J. Lab. clin. Med. 50, 469–477 (1957).
3. Arthurton, M. W., Meade, B. W.: Congenital galactosaemia. Report of a case. Brit. med. J. II, 618–620 (1954).
4. Ballabriga, A., Samso, J. M., Claret, I.: EEG et galactosemie experimentale. In “Modern Problems of Pediatrics”, Vol. 4, Basel and New York: S. Karger 1959.
5. Bauer, R.: Weitere Untersuchungen über alimentäre Galaktosurie. Wien. med. Wschr. 56, 2538–2546 (1906).