接受饮食治疗的苯丙酮尿症和枫糖尿症患者的微量元素紊乱 - Suppr

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超能文献

Trace element disturbances in dietetically treated patients with phenylketonuria and maple syrup urine disease.

作者信息

Lombeck I, Kasperek K, Feinendegen L E, Bremer H J

出版信息

Monogr Hum Genet. 1978;9:114-7. doi: 10.1159/000401620.

DOI:10.1159/000401620

PMID:732826

Abstract

摘要

相似文献

Trace element disturbances in dietetically treated patients with phenylketonuria and maple syrup urine disease.接受饮食治疗的苯丙酮尿症和枫糖尿症患者的微量元素紊乱

Monogr Hum Genet. 1978;9:114-7. doi: 10.1159/000401620.

The selenium state of children. II. Selenium content of serum, whole blood, hair and the activity of erythrocyte glutathione peroxidase in dietetically treated patients with phenylketonuria and maple-syrup-urine disease.儿童的硒状态。II. 饮食治疗的苯丙酮尿症和枫糖尿症患者的血清、全血、头发中的硒含量及红细胞谷胱甘肽过氧化物酶活性

Eur J Pediatr. 1978 Jul 19;128(4):213-23. doi: 10.1007/BF00445606.

Serum-selenium concentrations in patients with maple-syrup-urine disease and phenylketonuria under dieto-therapy.接受饮食治疗的枫糖尿症和苯丙酮尿症患者的血清硒浓度。

Clin Chim Acta. 1975 Oct 1;64(1):57-61. doi: 10.1016/0009-8981(75)90144-8.

Plasma glutathione peroxidase after selenium supplementation in patients with reduced selenium state.

Eur J Pediatr. 1982 Mar;138(2):138-40. doi: 10.1007/BF00441140.

Glutathione peroxidase and glutathione S-transferase activity of platelets.血小板的谷胱甘肽过氧化物酶和谷胱甘肽S-转移酶活性

Eur J Pediatr. 1983 Jun-Jul;140(3):244-7. doi: 10.1007/BF00443370.

Selenium requirements in patients with inborn errors of amino acid metabolism and selenium deficiency.氨基酸代谢先天性缺陷及硒缺乏患者的硒需求

Eur J Pediatr. 1980 Jun;134(1):65-8. doi: 10.1007/BF00442405.

Control of pyruvate and beta-hydroxybutyrate utilization in rat brain mitochondria and its relevance to phenylketonuria and maple syrup urine disease.大鼠脑线粒体中丙酮酸和β-羟基丁酸利用的调控及其与苯丙酮尿症和枫糖尿症的相关性。

J Neurochem. 1976 Apr;26(4):823-30. doi: 10.1111/j.1471-4159.1976.tb04458.x.

The need of essential amino acids in children. An evaluation based on the intake of phenylalanine, tyrosine, leucine, isoleucine, and valine in children with phenylketonuria, tyrosine amino transferase defect, and maple syrup urine disease.儿童对必需氨基酸的需求。基于苯丙酮尿症、酪氨酸氨基转移酶缺陷症和枫糖尿症患儿苯丙氨酸、酪氨酸、亮氨酸、异亮氨酸和缬氨酸摄入量的评估。

Am J Clin Nutr. 1980 Feb;33(2):279-86. doi: 10.1093/ajcn/33.2.279.

Trace element nutrition status and dietary intake of children with phenylketonuria.苯丙酮尿症患儿的微量元素营养状况及膳食摄入量

Am J Clin Nutr. 1990 Jul;52(1):159-65. doi: 10.1093/ajcn/52.1.159.

Transaminations between amino acids and keto acids elevated in phenylketonuria and maple syrup urine disease.

J Neurochem. 1973 Feb;20(2):389-403. doi: 10.1111/j.1471-4159.1973.tb12138.x.

引用本文的文献

Phenylketonuria oxidative stress and energy dysregulation: Emerging pathophysiological elements provide interventional opportunity.苯丙酮尿症氧化应激和能量失调：新兴的病理生理因素提供了干预机会。

Mol Genet Metab. 2022 Jun;136(2):111-117. doi: 10.1016/j.ymgme.2022.03.012. Epub 2022 Mar 29.

The zinc, copper, and manganese status of children with malabsorption syndromes and inborn errors of metabolism.吸收不良综合征和先天性代谢错误患儿的锌、铜、锰状态。

Biol Trace Elem Res. 1982 Jun;4(2-3):157-73. doi: 10.1007/BF02783255.

Zinc status and growth of children undergoing treatment for phenylketonuria.苯丙酮尿症患儿治疗期间的锌状态与生长情况

J Inherit Metab Dis. 1982;5(2):107-10. doi: 10.1007/BF01800002.

J Inherit Metab Dis. 1986;9 Suppl 2:183-201. doi: 10.1007/BF01799703.

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