酮症性高甘氨酸血症患者的丙酸血症 - Suppr

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Propionic acidemia in patients with ketotic hyperglycinemia.

作者信息

Ando T, Rasmussen K, Nyhan W L, Donnell G N, Barnes N D

出版信息

J Pediatr. 1971 May;78(5):827-32. doi: 10.1016/s0022-3476(71)80354-2.

DOI:10.1016/s0022-3476(71)80354-2

PMID:5581587

Abstract

摘要

相似文献

Propionic acidemia in patients with ketotic hyperglycinemia.酮症性高甘氨酸血症患者的丙酸血症

J Pediatr. 1971 May;78(5):827-32. doi: 10.1016/s0022-3476(71)80354-2.

The oxidation of glycine and propionic acid in propionic acidemia with ketotic hyperglycinemia.

Pediatr Res. 1972 Jun;6(6):576-83. doi: 10.1203/00006450-197206000-00006.

Hyperglycinemia and propionyl coA carboxylase deficiency and episodic severe illness without consistent ketosis.

J Pediatr. 1975 May;86(5):707-12. doi: 10.1016/s0022-3476(75)80354-4.

[Propionic acidemia. New concept of hyperglycinemia with ketosis].[丙酸血症。伴有酮症的高甘氨酸血症的新概念]

Pediatrie. 1972 Mar;27(2):217-20.

[Hyperglycinemia in clinical-laboratory practice].

Pediatr Med Chir. 1997 Mar-Apr;19(2):109-12.

Propionic acidemia and anorectal anomalies in three siblings.

Am J Dis Child. 1977 Dec;131(12):1379-81. doi: 10.1001/archpedi.1977.02120250061009.

Methylmalonic aciduria. An inborn error leading to metabolic acidosis, long-chain ketonuria and intermittent hyperglycinemia.甲基丙二酸尿症。一种导致代谢性酸中毒、长链酮尿症和间歇性高甘氨酸血症的先天性疾病。

N Engl J Med. 1968 Jun 13;278(24):1319-22. doi: 10.1056/NEJM196806132782404.

Beta-ketothiolase deficiency as a cause of the "ketotic hyperglycinemia syndrome".β-酮硫解酶缺乏症作为“酮症高甘氨酸血症综合征”的一个病因

Pediatrics. 1974 Feb;53(2):221-5.

Localisation of enzymic defect in propionicacidaemia.丙酸血症中酶缺陷的定位

Lancet. 1970 May 30;1(7657):1140-3. doi: 10.1016/s0140-6736(70)91216-x.

A block in glycine cleavage reaction as a common mechanism in ketotic and nonketotic hyperglycinemia.甘氨酸裂解反应受阻作为酮症和非酮症高甘氨酸血症的共同机制。

Pediatr Res. 1974 Jul;8(7):721-3. doi: 10.1203/00006450-197407000-00007.

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Understanding acute metabolic decompensation in propionic and methylmalonic acidemias: a deep metabolic phenotyping approach.理解丙酸血症和甲基丙二酸血症中的急性代谢失代偿：一种深入的代谢表型分析方法。

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Inborn errors of metabolism associated with hyperglycaemic ketoacidosis and diabetes mellitus: narrative review.与高血糖酮症酸中毒和糖尿病相关的先天性代谢缺陷：叙述性综述

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Reevaluating the hype: four bacterial metabolites under scrutiny.重新审视炒作：四种受审查的细菌代谢产物。

Eur J Microbiol Immunol (Bp). 2015 Mar;5(1):1-13. doi: 10.1556/EUJMI-D-14-00030. Epub 2015 Mar 26.

Clinical outcome and long-term management of 17 patients with propionic acidaemia.17例丙酸血症患者的临床结局及长期管理

Eur J Pediatr. 1996 Mar;155(3):205-10. doi: 10.1007/BF01953939.

Absence of cross-reacting material in isolated propionyl CoA carboxylase deficiency: nature of residual carboxylating activity.孤立性丙酰辅酶A羧化酶缺乏症中交叉反应物质的缺失：残余羧化活性的性质

Am J Hum Genet. 1983 May;35(3):409-20.

Effect of chain length of short-chain fatty acids on their effect on intracranial pressure in rabbits.短链脂肪酸链长度对其影响家兔颅内压的作用

J Neurol Neurosurg Psychiatry. 1982 May;45(5):428-30. doi: 10.1136/jnnp.45.5.428.

Tiglicaciduria in propionicacidaemia.丙酸血症中的惕各酸尿症

Biochem J. 1972 Feb;126(4):1035-7. doi: 10.1042/bj1261035.

Inborn errors of metabolism: principles and their applications.先天性代谢缺陷：原理及其应用

Can Med Assoc J. 1972 Mar 18;106(6):677 passim.

3-hydroxypropionate: significance of -oxidation of propionate in patients with propionic acidemia and methylmalonic acidemia.3-羟基丙酸：丙酸血症和甲基丙二酸血症患者中丙酸β氧化的意义

Proc Natl Acad Sci U S A. 1972 Oct;69(10):2807-11. doi: 10.1073/pnas.69.10.2807.

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