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Cerebral MRI in 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: case report.

作者信息

Ferris N J, Tien R D

机构信息

Department of Radiology, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Neuroradiology. 1993;35(7):559-60. doi: 10.1007/BF00588725.

DOI:10.1007/BF00588725
PMID:8232893
Abstract
摘要

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本文引用的文献

1
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.
2
Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.3-羟基-3-甲基戊二酰辅酶A裂解酶缺乏症的非典型表现及神经病理学研究
Ann Neurol. 1986 Sep;20(3):367-9. doi: 10.1002/ana.410200318.
3
Capacity for substrate utilization in oxidative metabolism by neurons, astrocytes, and oligodendrocytes from developing brain in primary culture.
原代培养中发育中大脑的神经元、星形胶质细胞和少突胶质细胞在氧化代谢中利用底物的能力。
J Neurosci Res. 1987;18(4):551-61. doi: 10.1002/jnr.490180407.
4
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients.3-羟基-3-甲基戊二酰辅酶A裂解酶缺乏症：18例报告患者的综述
Eur J Pediatr. 1988 Dec;148(3):180-6. doi: 10.1007/BF00441397.
5
3-Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) lyase deficiency in Saudi Arabia.沙特阿拉伯的3-羟基-3-甲基戊二酰辅酶A（HMG-CoA）裂解酶缺乏症。
J Inherit Metab Dis. 1991;14(2):174-88. doi: 10.1007/BF01800590.