Fructosaemia: an inborn error of fructose metabolism.
作者信息
LEVIN B, OBERHOLZER V G, SNODGRASS G J, STIMMLER L, WILMERS M J
出版信息
Arch Dis Child. 1963 Jun;38(199):220-30. doi: 10.1136/adc.38.199.220.
Abstract
摘要
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Arch Dis Child. 1963 Jun;38(199):220-30. doi: 10.1136/adc.38.199.220.
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本文引用的文献
1
Hereditary fructose intolerance, an inborn deficiency of liver aldolase complex.
Metabolism. 1962 Jul;11:727-31.
2
The amino-aciduria in galactosaemia.半乳糖血症中的氨基酸尿症。
Arch Dis Child. 1955 Apr;30(150):150-4. doi: 10.1136/adc.30.150.150.
3
[Hereditary intolerance to fructose. Apropos of a case].
Pediatrie. 1961;16:605-26.
4
[Study of a case of functional hypoglycemia caused by intolerance to fructose].[果糖不耐受所致功能性低血糖1例研究]
Helv Paediatr Acta. 1961 Apr;16:90-6.
5
Familial fructose and galactose intolerance.
Lancet. 1961 Jun 3;1(7188):1189-94. doi: 10.1016/s0140-6736(61)91940-7.
6
[Congenital hereditary fructose intolerance].先天性遗传性果糖不耐受症
Klin Wochenschr. 1959 Jul 1;37(13):693-6. doi: 10.1007/BF01478217.
7
[Galactose disease; genetic considerations; study of aminoacidemia & aminoacidura].
Arch Fr Pediatr. 1959;16(2):158-84.
8
Studies of erythrocyte phosphate ester metabolism in galactosaemia.半乳糖血症中红细胞磷酸酯代谢的研究。
Clin Sci. 1958 Aug;17(3):385-91.
9
Bovine liver aldolase. I. Isolation, crystallization, and some general properties.
J Biol Chem. 1958 Aug;233(2):365-70.
10
Clinical applications of amino-acid chromatography.
Scand J Clin Lab Invest. 1958;10 Suppl 31:122-7.
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