Chronic congenital lactic acidosis. A fatal case with hyperphosphatemia and hyperlipemia.
作者信息
Schärer K, Marty A, Mühlethaler J P
出版信息
Helv Paediatr Acta. 1968 Apr;23(2):107-27.
PMID:5699019
Abstract
摘要
相似文献
1
Chronic congenital lactic acidosis. A fatal case with hyperphosphatemia and hyperlipemia.
Helv Paediatr Acta. 1968 Apr;23(2):107-27.
2
Familial chronic acidosis due to an error in lactate and pyruvate metabolism.由于乳酸和丙酮酸代谢错误导致的家族性慢性酸中毒。
Can Med Assoc J. 1967 Sep 23;97(13):773-9.
3
[Congenital chronic lactic acid acidosis].
Monatsschr Kinderheilkd (1902). 1968 Jun;116(6):304-5.
4
Fatal congenital lactic acidosis in two siblings. II. Biochemical studies in vivo and in vitro.
Acta Paediatr Scand. 1971 Mar;60(2):138-45. doi: 10.1111/j.1651-2227.1971.tb06633.x.
5
[Congenital lactic acidosis. First national comunic- ation].[先天性乳酸酸中毒。首次全国性报告]
Prensa Med Argent. 1967 Sep 22;54(30):1648-52.
6
7
Recurrent attacks of ketoacidosis with hyperlacticacidaemia, hyperpyruvicacidaemia and hyperalaninaemia.伴有高乳酸血症、高丙酮酸血症和高丙氨酸血症的酮症酸中毒反复发作。
Acta Paediatr Belg. 1973;27(1):21-9.
8
[A case of congenital lactic acidosis caused by deficiency of pyruvate dehydrogenase].[一例因丙酮酸脱氢酶缺乏导致的先天性乳酸性酸中毒病例]
Minerva Pediatr. 1979 Nov 15;31(21):1539-46.
9
[Organic acidemias: current diagnostic practical possibilities].
Pediatria (Napoli). 1983 Jan-Mar;91(1):3-13.
10
Urinary organic acids in a case of congenital lactic acidosis due to pyruvate decarboxylase deficiency.一例因丙酮酸脱羧酶缺乏导致的先天性乳酸酸中毒患者的尿有机酸分析
J Inherit Metab Dis. 1978;1(1):15-6. doi: 10.1007/BF01805708.
引用本文的文献
1
[Familial leukoencephalopathy associated with congenital lactic acidosis].
Acta Neuropathol. 1971;17(2):156-68. doi: 10.1007/BF00687491.
2
An inherited defect affecting the tricarboxylic acid cycle in a patient with congenital lactic acidosis.一名患有先天性乳酸性酸中毒的患者存在影响三羧酸循环的遗传性缺陷。
J Clin Invest. 1972 Jul;51(7):1845-51. doi: 10.1172/JCI106986.
Zotero 插件