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Biochemical studies and therapy in subacute necrotizing encephalomyelopathy (Leigh's syndrome).

作者信息

Grover W D, Auerbach V H, Patel M S

出版信息

J Pediatr. 1972 Jul;81(1):39-44. doi: 10.1016/s0022-3476(72)80371-8.

DOI:10.1016/s0022-3476(72)80371-8
PMID:4556192
Abstract
摘要

相似文献

1
Biochemical studies and therapy in subacute necrotizing encephalomyelopathy (Leigh's syndrome).亚急性坏死性脑脊髓病（ Leigh 综合征）的生化研究与治疗
J Pediatr. 1972 Jul;81(1):39-44. doi: 10.1016/s0022-3476(72)80371-8.
2
Subacute necrotizing encephalomyelopathy (Leigh's disease): a consideration of clinical features and etiology.亚急性坏死性脑脊髓病（ Leigh 病）：临床特征与病因学探讨
Dev Med Child Neurol. 1972 Feb;14(1):87-101. doi: 10.1111/j.1469-8749.1972.tb02563.x.
3
Pathogenesis of Leigh's encephalomyelopathy.Leigh 脑脊髓病的发病机制。
J Pediatr. 1972 Jul;81(1):189-90. doi: 10.1016/s0022-3476(72)80428-1.
4
[Leigh's syndrome].
Monatsschr Kinderheilkd (1902). 1974 Jan;122(1):44-5.
5
Further speculation on the pathogenesis of Leigh's encephalomyelopathy.
J Pediatr. 1973 Mar;82(3):541-2. doi: 10.1016/s0022-3476(73)80144-1.
6
Letter: Leigh's disease: A family study.
Lancet. 1976 Jun 5;1(7971):1237. doi: 10.1016/s0140-6736(76)92180-2.
7
The effect of thiamine treatment on the activity of pyruvate dehydrogenase: relation of the treatment of Leigh's encephalomyelopathy.
Pediatr Res. 1973 Jul;7(7):616-9. doi: 10.1203/00006450-197307000-00003.
8
Letter: Biochemical abnormalities in Leigh's disease.
Lancet. 1976 Jun 5;1(7971):1237-8. doi: 10.1016/s0140-6736(76)92181-4.
9
Normal activities of hepatic pyruvate dehydrogenase and pyruvate carboxylase in Leigh's syndrome.Leigh综合征中肝丙酮酸脱氢酶和丙酮酸羧化酶的正常活性
Tohoku J Exp Med. 1983 Jan;139(1):67-72. doi: 10.1620/tjem.139.67.
10
[Subacute necrotizing encephalomyelopathy (Leigh's disease) (author's transl)].
Monatsschr Kinderheilkd (1902). 1975 Feb;123(2):84-90.

引用本文的文献

1
Erythrocyte transketolase activity in suspected cases of Leigh's disease, or subacute necrotising encephalomyelopathy.疑似 Leigh 病或亚急性坏死性脑脊髓病病例中的红细胞转酮醇酶活性。
Arch Dis Child. 1980 Oct;55(10):789-94. doi: 10.1136/adc.55.10.789.
2
Megavitamin therapy in inherited metabolic disorders.遗传性代谢紊乱中的大剂量维生素疗法。
Indian J Pediatr. 1981 Sep-Oct;48(394):635-46. doi: 10.1007/BF02821592.
3
Hepatic, gut, and renal substrate flux rates in patients with hepatic cirrhosis.肝硬化患者的肝脏、肠道和肾脏底物通量率
J Clin Invest. 1981 Jul;68(1):240-52. doi: 10.1172/jci110240.
4
X-linked Leigh's syndrome.X连锁 Leigh 综合征
Hum Genet. 1982;62(1):52-9. doi: 10.1007/BF00295603.
5
Leigh's disease with decreased activities of pyruvate carboxylase and pyruvate decarboxylase.伴有丙酮酸羧化酶和丙酮酸脱羧酶活性降低的 Leigh 病
J Inherit Metab Dis. 1980;2(1):15-8. doi: 10.1007/BF01805557.
6
Is pyruvate carboxylase involved in the renal tubular reabsorption of bicarbonate?丙酮酸羧化酶是否参与肾小管对碳酸氢盐的重吸收？
J Inherit Metab Dis. 1980;3(4):113-6. doi: 10.1007/BF02312544.
7
Evidence for two genetic complementation groups in pyruvate carboxylase-deficient human fibroblast cell lines.丙酮酸羧化酶缺陷型人成纤维细胞系中两个遗传互补组的证据。
Biochem Genet. 1980 Jun;18(5-6):617-24. doi: 10.1007/BF00484405.
8
Neonatal pyruvate carboxylase deficiency with renal tubular acidosis and cystinuria.新生儿丙酮酸羧化酶缺乏伴肾小管酸中毒和胱氨酸尿症。
J Inherit Metab Dis. 1983;6(3):89-94. doi: 10.1007/BF01800731.
9
The biotin-dependent carboxylase deficiencies.生物素依赖性羧化酶缺乏症
Am J Hum Genet. 1982 Sep;34(5):699-716.
10
Studies on cultured fibroblasts from patients with defects of biotin-dependent carboxylation.
J Inherit Metab Dis. 1981;4(4):183-9. doi: 10.1007/BF02263649.