婴儿猝死与脂肪氧化遗传性疾病 - Suppr

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超能文献

Sudden infant death and inherited disorders of fat oxidation.

出版信息

Lancet. 1986 Nov 8;2(8515):1073-5.

PMID:2877228

Abstract

摘要

相似文献

Sudden infant death and inherited disorders of fat oxidation.婴儿猝死与脂肪氧化遗传性疾病

Lancet. 1986 Nov 8;2(8515):1073-5.

[Do defects in fatty acid oxidation cause sudden infant death?].脂肪酸氧化缺陷会导致婴儿猝死吗？

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Fatty acid oxidation defects as causes of unexpected death in infancy.脂肪酸氧化缺陷作为婴儿意外死亡的原因

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Sudden infant death syndrome and inherited disorders of fatty acid beta-oxidation.婴儿猝死综合征与脂肪酸β氧化的遗传性疾病

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引用本文的文献

Is the medium-chain acyl-CoA dehydrogenase G985 mutation involved in sudden infant death in Norway?

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Br Med J (Clin Res Ed). 1988 Jan 2;296(6614):11-2. doi: 10.1136/bmj.296.6614.11.

The inborn errors of mitochondrial fatty acid oxidation.线粒体脂肪酸氧化的先天性代谢缺陷。

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Comparison of urinary acylglycines and acylcarnitines as diagnostic markers of medium-chain acyl-CoA dehydrogenase deficiency.尿酰基甘氨酸和酰基肉碱作为中链酰基辅酶A脱氢酶缺乏症诊断标志物的比较。

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Generalised dicarboxylic aciduria: a common finding in neonates.

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Disorders of mitochondrial beta-oxidation: prenatal and early postnatal diagnosis and their relevance to Reye's syndrome and sudden infant death.线粒体β-氧化紊乱：产前及产后早期诊断及其与瑞氏综合征和婴儿猝死的相关性

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Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblings.新生儿中链酰基辅酶A脱氢酶缺乏症的早期诊断与治疗：两例同胞病例报告

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The phenylpropionic acid load test: experience with 72 children at-risk for beta-oxidation disorders.

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