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[Enteral absorption of phenylalanine in healthy subjects and phenylketonurics].

作者信息

Theile H, Beyreiss K

出版信息

Klin Wochenschr. 1967 Jul 1;45(13):687-8. doi: 10.1007/BF01747207.

DOI:10.1007/BF01747207
PMID:5589239
Abstract
摘要

相似文献

1
[Enteral absorption of phenylalanine in healthy subjects and phenylketonurics].
Klin Wochenschr. 1967 Jul 1;45(13):687-8. doi: 10.1007/BF01747207.
2
Kinetics of phenylalanine disappearance after intravenous load in phenylketonuria and its genetic variants.苯丙酮尿症及其基因变异患者静脉注射负荷后苯丙氨酸消失的动力学
Pediatr Res. 1979 Jan;13(1):21-5. doi: 10.1203/00006450-197901000-00005.
3
Developmental changes of cerebral phenylalanine uptake from severely elevated blood levels.
Neurochem Res. 1984 Jun;9(6):837-48. doi: 10.1007/BF00965670.
4
[Phenylketonuria and hyperphenylalaninemia. Introduction to the subject].
Minerva Nipiol. 1970 Sep-Oct;20(5):112-43.
5
[Study of blood amino acids during a phenylalanine loading test].[苯丙氨酸负荷试验期间血液氨基酸的研究]
Biomedicine. 1975 Apr 30;23(4):149-54.
6
Metabolic conversion of L-[U-14C]phenylalanine to respiratory 14CO2 in healthy subjects, phenylketonuria heterozygotes and classic phenylketonurics.
Clin Chim Acta. 1986 Jun 30;157(3):253-66. doi: 10.1016/0009-8981(86)90301-3.
7
Pathogenesis of different clinical outcomes in spite of identical genotypes and comparable blood phenylalanine concentrations in phenylketonurics.尽管苯丙酮尿症患者具有相同的基因型和相近的血苯丙氨酸浓度,但仍出现不同临床结局的发病机制。
J Inherit Metab Dis. 1998 Apr;21(2):181-2. doi: 10.1023/a:1005328717095.
8
[Intestinal absorption of amino acids in phenylketonuric subjects studied with the continuous intestinal perfusion method].
Pathol Biol (Paris). 1972 Jun-Jul;20(11):543-50.
9
Semen studies on phenylketonurics.苯丙酮尿症患者的精液研究。
Biochem Med. 1981 Dec;26(3):427-34. doi: 10.1016/0006-2944(81)90017-x.
10
[Some indices of phenylalanine and tyrosine metabolism in children with phenylketonuria].
Vopr Okhr Materin Det. 1969;14(7):29-32.

本文引用的文献

1
An enzymatic spectrophotometric method for the determination of phenylalanine in blood.一种用于测定血液中苯丙氨酸的酶促分光光度法。
J Lab Clin Med. 1960 Mar;55:491-6.
2
Detection of heterozygotes for phenylketonuria.苯丙酮尿症杂合子的检测。
Clin Chim Acta. 1960 Jul;5:471-6. doi: 10.1016/0009-8981(60)90054-1.
3
[FREE PLASMA AMINO ACIDS AND BLOOD AMMONIA FOLLOWING ORAL PROTEIN LOAD. STUDIES IN NORMAL PERSONS AND PATIENTS WITH LIVER CIRRHOSIS].[口服蛋白质负荷后的游离血浆氨基酸和血氨。对正常人和肝硬化患者的研究]
Klin Wochenschr. 1965 Apr 1;43:382-90. doi: 10.1007/BF01484659.
4
Accumulation of L-phenylalanine by segments of small intestine.小肠各段对L-苯丙氨酸的蓄积
Am J Physiol. 1961 Mar;200:505-7. doi: 10.1152/ajplegacy.1961.200.3.505.
5
[Studies of the utilization of parenterally administered amino acid solutions].[胃肠外营养用氨基酸溶液的应用研究]
Klin Wochenschr. 1966 Aug 15;44(16):929-43. doi: 10.1007/BF01711465.
6
[Research on the tyrosine metabolism of premature infants. I. Changes in blood tyrosine and phenylalanine levels in premature infants during the 1st weeks of life].[早产儿酪氨酸代谢的研究。I. 早产儿出生后第一周内血液酪氨酸和苯丙氨酸水平的变化]
Ann Paediatr. 1966;206(1):12-27.
7
Biochemical and EEG studies in phenylketonuric children during phenylalanine tolerance testc.苯丙酮尿症患儿在苯丙氨酸耐量试验期间的生化和脑电图研究
Arch Dis Child. 1966 Jun;41(217):267-72. doi: 10.1136/adc.41.217.267.
8
Tolerance of phenylalanine after ntravenous administration in phenylketonurics, heterozygous carriers, and normal adults.
Nature. 1966 Mar 12;209(5028):1148-9. doi: 10.1038/2091148a0.