beta-Hydroxy-beta-methyglutaricaciduria presenting as Reye's syndrome.

Suppr

超能文献

作者信息

Leonard J V, Seakins J W, Griffin N K

出版信息

Lancet. 1979 Mar 24;1(8117):680. doi: 10.1016/s0140-6736(79)91137-1.

DOI:10.1016/s0140-6736(79)91137-1

PMID:85928

Abstract

摘要

相似文献

beta-Hydroxy-beta-methyglutaricaciduria presenting as Reye's syndrome.

Lancet. 1979 Mar 24;1(8117):680. doi: 10.1016/s0140-6736(79)91137-1.

Organic acids and Reye's syndrome.

Lancet. 1979 May 26;1(8126):1147. doi: 10.1016/s0140-6736(79)91825-7.

Reye's syndrome and aspirin: epidemiological associations and inborn errors of metabolism.

Lancet. 1987 Aug 22;2(8556):429-31.

Partial carbamyl phosphate synthetase deficiency, simulating Reye's syndrome, in a 9-year-old girl.

Isr J Med Sci. 1986 Jun;22(6):463-5.

Recurrent Reye's syndrome without liver lipid deposition.

Hosp Pract (Hosp Ed). 1981 Feb;16(2):45-51. doi: 10.1080/21548331.1981.11946724.

beta-hydroxy-beta-methylglutaricaciduria, Reye's syndrome, and Echovirus 11.β-羟基-β-甲基戊二酸尿症、瑞氏综合征和埃可病毒11型。

Lancet. 1979 May 26;1(8126):1147. doi: 10.1016/s0140-6736(79)91826-9.

Masking by enzyme inhibitor of raised serum glutamate dehydrogenase activity in Reye's syndrome.

Lancet. 1983 Jul 2;2(8340):4-7. doi: 10.1016/s0140-6736(83)90002-8.

Differential diagnosis of Reye's syndrome.瑞氏综合征的鉴别诊断。

Dev Med Child Neurol. 1987 Feb;29(1):110-6. doi: 10.1111/j.1469-8749.1987.tb02115.x.

A Reye's syndrome like illness with early seizures: its relationship to Reye's syndrome.一种伴有早期癫痫发作的类瑞氏综合征疾病：它与瑞氏综合征的关系。

J Singapore Paediatr Soc. 1982;24(1-2):33-53.

Inborn errors of metabolism in children referred with Reye's syndrome. A changing pattern.患有瑞氏综合征儿童的先天性代谢缺陷。一种不断变化的模式。

JAMA. 1988 Dec 2;260(21):3167-70.

引用本文的文献

Hepatic Manifestations of 3-Hydroxy-3-Methylglutaryl-Coenzyme-A Lyase Deficiency in Saudi Patients: Experience of a Tertiary Care Center.沙特患者3-羟基-3-甲基戊二酰辅酶A裂解酶缺乏症的肝脏表现：一家三级医疗中心的经验

J Pediatr Genet. 2021 Jun;10(2):105-110. doi: 10.1055/s-0040-1714698. Epub 2020 Jul 29.

Inherited disorders of 3-methylcrotonyl CoA carboxylation.3-甲基巴豆酰辅酶A羧化酶遗传性疾病。

Arch Dis Child. 1981 Jan;56(1):53-9. doi: 10.1136/adc.56.1.53.

3-hydroxy-3-methylglutaryl-CoA lyase deficiency in an infant with macrocephaly and mild metabolic acidosis.一名患有巨头畸形和轻度代谢性酸中毒的婴儿出现3-羟基-3-甲基戊二酰辅酶A裂解酶缺乏症。

Eur J Pediatr. 1982 Feb;138(1):73-6. doi: 10.1007/BF00442334.

Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.鸟氨酸氨甲酰基转移酶缺乏症患儿的神经学特征及脑部计算机断层扫描

J Neurol Neurosurg Psychiatry. 1983 Jan;46(1):28-34. doi: 10.1136/jnnp.46.1.28.

A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.一名患有急性胰腺炎且因3-羟基-3-甲基戊二酰辅酶A裂解酶缺乏症而反复出现低血糖的儿童。

Eur J Pediatr. 1984 Sep;142(4):289-91. doi: 10.1007/BF00540255.

Genetic complementation analysis of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency in cultured fibroblasts.培养成纤维细胞中3-羟基-3-甲基戊二酰辅酶A裂解酶缺乏症的基因互补分析

Am J Hum Genet. 1984 Jul;36(4):791-801.

CT findings in a case of deficiency of 3-hydroxy-3-methylglutaryl-CoA-lyase.3-羟基-3-甲基戊二酰辅酶A裂解酶缺乏症一例的CT表现

Neuroradiology. 1981;22(2):99-101. doi: 10.1007/BF00344781.

Effect of Reye's syndrome serum on isolated chinchilla liver mitochondria.瑞氏综合征血清对离体龙猫肝线粒体的影响。

J Clin Invest. 1985 Aug;76(2):816-25. doi: 10.1172/JCI112039.

Reye syndrome.瑞氏综合征

Neurol Clin. 1985 Feb;3(1):95-115. doi: 10.1016/S0733-8619(18)31058-2.

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency.

J Inherit Metab Dis. 1986;9(3):287-8. doi: 10.1007/BF01799665.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验