年龄对苯丙酮尿症及其基因变异型中邻羟基苯乙酸排泄的影响。 - Suppr

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超能文献

Influence of age on ortho-hydroxyphenylacetic acid excretion in phenylketonuria and its genetic variants.

作者信息

Rey F, Pellié C, Sivy M, Blandin-Savoja F, Rey J, Frézal J

出版信息

Pediatr Res. 1974 May;8(5):540-5. doi: 10.1203/00006450-197405000-00002.

DOI:10.1203/00006450-197405000-00002

PMID:4151091

Abstract

摘要

相似文献

Influence of age on ortho-hydroxyphenylacetic acid excretion in phenylketonuria and its genetic variants.年龄对苯丙酮尿症及其基因变异型中邻羟基苯乙酸排泄的影响。

Pediatr Res. 1974 May;8(5):540-5. doi: 10.1203/00006450-197405000-00002.

[Relationship of urinary phenylpyruvate and o-hydroxyphenylacetate on serum phenylalanine level in patients with phenylketonuria treated by diet].[饮食治疗苯丙酮尿症患者中尿苯丙酮酸和邻羟基苯乙酸与血清苯丙氨酸水平的关系]

Cas Lek Cesk. 1975 Apr 25;114(17):518-21.

Aromatic acid excretion in classical phenylketonuria and hyperphenylalaninemic variants.经典型苯丙酮尿症和高苯丙氨酸血症变异型中的芳香酸排泄

Helv Paediatr Acta. 1974 Nov;29(5):489-98.

[Relations between serum phenylalanine level and phenylpyruvate and o-hydroxyphenylacetate in urine of patients with phenylketonuria, treated by diet].

Bratisl Lek Listy. 1971;55(1):63-9.

[Phenylpyruvate and o-hydroxyphenylacetate in the urine of phenylketonurics treated by dietary measures].[通过饮食措施治疗的苯丙酮尿症患者尿液中的苯丙酮酸和邻羟基苯乙酸]

Z Kinderheilkd. 1970;108(3):258-64.

Aromatic acids in urine of healthy infants, persistent hyperphenylalaninemia, and phenylketonuria, before and after phenylalanine load.苯丙氨酸负荷前后健康婴儿、持续性高苯丙氨酸血症和苯丙酮尿症尿液中的芳香酸。

Pediatr Res. 1974 Jul;8(7):704-9. doi: 10.1203/00006450-197407000-00003.

[Phenylalanine hydroxylase activity in the livers of patients with phenylketonuria].[苯丙酮尿症患者肝脏中的苯丙氨酸羟化酶活性]

Vopr Med Khim. 1974 Nov-Dec;20(6):656-60.

Absence of a significant renal threshold for two aromatic acids in phenylketonuric children over two years of age.

Eur J Pediatr. 1980 Aug;134(2):115-8. doi: 10.1007/BF01846027.

Quantitative analysis of phenylalanine metabolites in urine to detect heterozygotes of phenylketonuria.尿中苯丙氨酸代谢产物的定量分析以检测苯丙酮尿症杂合子。

Humangenetik. 1974 Apr 24;22(1):85-8. doi: 10.1007/BF00338140.

[Diet in phenylketonuria].[苯丙酮尿症的饮食]

Arch Fr Pediatr. 1969 Aug-Sep;26(7):791-807.

引用本文的文献

Development of Metabolic Phenotype in Phenylketonuria: Evaluation of the Blaskovics Protein Loading Test at 5 Years of Age.苯丙酮尿症代谢表型的发展：5岁时布拉斯科维茨蛋白负荷试验的评估

JIMD Rep. 2016;29:77-84. doi: 10.1007/8904_2015_508. Epub 2015 Dec 19.

Isolated persistent hypermethioninemia.孤立性持续性高甲硫氨酸血症

Am J Hum Genet. 1995 Oct;57(4):882-92.

Absence of a significant renal threshold for two aromatic acids in phenylketonuric children over two years of age.

Eur J Pediatr. 1980 Aug;134(2):115-8. doi: 10.1007/BF01846027.

Examination of urine metabolites in the newborn period and during protein loading tests at 6 months of age--Part 1.新生儿期及6月龄蛋白质负荷试验期间尿液代谢物的检测——第1部分。

Eur J Pediatr. 1990;149 Suppl 1:S17-24. doi: 10.1007/BF02126294.

A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria.苯丙酮尿症中苯丙氨酸非共轭酸性转氨代谢产物的综述。

J Inherit Metab Dis. 1992;15(1):136-44. doi: 10.1007/BF01800355.

[Urinary phenylalanine metabolites in hyperphenylalaninemia (author's transl)].高苯丙氨酸血症中的尿苯丙氨酸代谢产物（作者译）

Klin Wochenschr. 1976 Nov 1;54(21):1047-53. doi: 10.1007/BF01469250.

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