Plasma Polyol Levels in Patients with Cataract
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Publisher
Springer Netherlands
Link
http://link.springer.com/content/pdf/10.1007/978-94-009-2175-7_13.pdf
Reference14 articles.
1. Brivet, M., Abadie, V., Soni, T., Cheron, G. and Dufier, J. L. Inexplicable infantile cataracts and partial maternal galactose disorder. Arch. Dis. Child. 61 (1986) 445–448
2. Harley, J. D., Mutton, P., Irvine, S. and Gupta, J. D. Maternal enzymes of galactose metabolism and the ‘inexplicable’ infantile cataract. Lancet 2 (1974) 259–261
3. Holton, J. B., Gillett, M. G., MacFaul, R. and Young, R. Galactosaemia: a new severe variant due to uridine diphosphate galactose-4-epimerase deficiency. Arch. Dis. Child. 56 (1981) 885–887
4. Jakobs, C., Warner, T. G., Sweetman, L. and Nyhan, W. L. Stable isotope dilution analysis of galactitol in amniotic fluid: an accurate approach to the prenatal diagnosis of galactosemia. Pediatr. Res. 18 (1984) 714–718
5. Jakobs, C., Douwes, A. C., Kok, R. M., De Jong, A., Endres, W. and Shin, Y. S. Elevated plasma galactitol levels in patients with congenital cataracts without enzyme defects. Eur. J. Pediatr. 147 (1988) 446
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