亚急性坏死性脑脊髓病（ Leigh 综合征）中的肾功能研究及肾脏丙酮酸羧化酶 - Suppr

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超能文献

Renal function studies and kidney pyruvate carboxylase in subacute necrotizing encephalomyelopathy (Leigh's syndrome).

作者信息

Gruskin A B, Patel M S, Linshaw M, Ettenger R, Huff D, Grover W

出版信息

Pediatr Res. 1973 Oct;7(10):832-41. doi: 10.1203/00006450-197310000-00007.

DOI:10.1203/00006450-197310000-00007

PMID:4747314

Abstract

摘要

相似文献

Renal function studies and kidney pyruvate carboxylase in subacute necrotizing encephalomyelopathy (Leigh's syndrome).亚急性坏死性脑脊髓病（ Leigh 综合征）中的肾功能研究及肾脏丙酮酸羧化酶

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引用本文的文献

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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.

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.

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.

Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.对28例患有乳酸酸中毒且与 Leigh 脑脊髓病相关的儿童进行的生化研究。

Eur J Pediatr. 1985 Mar;143(4):278-83. doi: 10.1007/BF00442301.

Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase.

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