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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- CUSWORTH D. C., DENT C. E., FLYNN F. V. The amino-aciduria in galactosaemia. Arch Dis Child. 1955 Apr;30(150):150–154. doi: 10.1136/adc.30.150.150. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DENT C. E. Clinical applications of amino-acid chromatography. Scand J Clin Lab Invest. 1958;10 (Suppl 31):122–127. [PubMed] [Google Scholar]
- DORMANDY T. L., PORTER R. J. Familial fructose and galactose intolerance. Lancet. 1961 Jun 3;1(7188):1189–1194. doi: 10.1016/s0140-6736(61)91940-7. [DOI] [PubMed] [Google Scholar]
- DUBOIS R., LOEB H., OOMS H. A., GILLET P., BARTMAN J., CHAMPENOIS A. [Study of a case of functional hypoglycemia caused by intolerance to fructose]. Helv Paediatr Acta. 1961 Apr;16:90–96. [PubMed] [Google Scholar]
- FROESCH E. R., PRADER A., LABHART A., STUBER H. W., WOLF H. P. Die hereditäre Fructoseintoleranz, eine bisher nicht bekannte kongenitale Stoffwechselstörung. Schweiz Med Wochenschr. 1957 Sep 14;87(37):1168–1171. [PubMed] [Google Scholar]
- JEUNE M., PLANSON E., COTTE J., BONNEFOY S., NIVELON J. L., SKOSOWSKY J. [Hereditary intolerance to fructose. Apropos of a case]. Pediatrie. 1961;16:605–626. [PubMed] [Google Scholar]
- NIKKILA E. A., SOMERSALO O., PITKANENE, PERHEENTUPA J. Hereditary fructose intolerance, an inborn deficiency of liver aldolase complex. Metabolism. 1962 Jul;11:727–731. [PubMed] [Google Scholar]
- PEANASKY R. J., LARDY H. A. Bovine liver aldolase. I. Isolation, crystallization, and some general properties. J Biol Chem. 1958 Aug;233(2):365–370. [PubMed] [Google Scholar]
- PENINGTON J. S., PRANKERD T. A. Studies of erythrocyte phosphate ester metabolism in galactosaemia. Clin Sci. 1958 Aug;17(3):385–391. [PubMed] [Google Scholar]
- TUNG T. C., LING K. H., BYRNE W. L., LARDY H. A. Substrate specificity of muscle aldolase. Biochim Biophys Acta. 1954 Aug;14(4):488–494. doi: 10.1016/0006-3002(54)90228-0. [DOI] [PubMed] [Google Scholar]
- VAN GEFFEL R., DEVRIENDT A., DUSTIN J. P., VIS H., LOEB H. La maladie du galactose; considerations génétiques; étude de l'amino-acidémie et de l'amino-acidurie. Arch Fr Pediatr. 1959;16(2):158–184. [PubMed] [Google Scholar]
- WOLF H., ZSCHOCKE D., WEDEMEYER F. W., HUBNER W. Angeborene hereditäre Fructose-Intoleranz. Klin Wochenschr. 1959 Jul 1;37(13):693–696. doi: 10.1007/BF01478217. [DOI] [PubMed] [Google Scholar]
