Biochemical screening in newborn siblings of cases of SIDS.
作者信息
Green A
机构信息
Department of Clinical Chemistry, West Midlands Regional Laboratory for Neonatal Screening and Inherited Metabolic Disorders, Children's Hospital, Birmingham.
出版信息
Arch Dis Child. 1993 Jun;68(6):793-6. doi: 10.1136/adc.68.6.793.
Abstract
摘要
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Biochemical screening in newborn siblings of cases of SIDS.对婴儿猝死综合征病例的新生同胞进行生化筛查。
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Is there a relation between SIDS and long QT syndrome?婴儿猝死综合征与长QT综合征之间有关系吗？
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本文引用的文献
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Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.长链酰基辅酶A脱氢酶缺乏症：非酮症低血糖的一种遗传病因。
Pediatr Res. 1985 Jul;19(7):666-71. doi: 10.1203/00006450-198507000-00006.
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Defects of metabolism of fatty acids in the sudden infant death syndrome.婴儿猝死综合征中脂肪酸代谢缺陷
Br Med J (Clin Res Ed). 1985 Jun 15;290(6484):1771-3. doi: 10.1136/bmj.290.6484.1771.
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Recurrence incidence of sudden infant death syndrome.婴儿猝死综合征的复发发生率。
Arch Dis Child. 1988 Aug;63(8):924-30. doi: 10.1136/adc.63.8.924.
4
Investigation of inborn errors of metabolism in unexpected infant deaths.意外婴儿死亡中先天性代谢缺陷的调查。
Lancet. 1988 Jul 2;2(8601):29-31. doi: 10.1016/s0140-6736(88)92955-8.
5
Screening siblings for inborn errors of fatty acid metabolism in families with a history of sudden infant death.对有婴儿猝死病史的家庭中的兄弟姐妹进行脂肪酸代谢先天性缺陷筛查。
Lancet. 1986;2(8521-22):1470. doi: 10.1016/s0140-6736(86)92794-7.
6
Sudden infant death syndrome and inherited disorders of fat metabolism.婴儿猝死综合征与脂肪代谢遗传性疾病
Lancet. 1986 Dec 6;2(8519):1332. doi: 10.1016/s0140-6736(86)91455-8.
7
Hepatic microsomal glucose-6-phosphatase system and sudden infant death syndrome.肝微粒体葡萄糖-6-磷酸酶系统与婴儿猝死综合征
Lancet. 1989 Aug 5;2(8658):291-4. doi: 10.1016/s0140-6736(89)90484-4.
8
Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase.婴儿猝死与长链3-羟基酰基辅酶A脱氢酶
Lancet. 1989 Jul 1;2(8653):52-3. doi: 10.1016/s0140-6736(89)90300-0.
9
Sudden, unexpected, natural death in childhood.儿童期突然、意外的自然死亡。
Pediatr Pathol. 1990;10(5):769-84. doi: 10.3109/15513819009064711.
10
The laboratory diagnosis of inborn errors of mitochondrial fatty acid oxidation.线粒体脂肪酸氧化先天性代谢缺陷的实验室诊断
Ann Clin Biochem. 1990 Nov;27 ( Pt 6):519-31. doi: 10.1177/000456329002700602.
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