165 related articles for article (PubMed ID: 4593262)
1. Thiamine-responsive lactic acidosis.
Nutr Rev; 1974 Mar; 32(3):95. PubMed ID: 4593262
[No Abstract] [Full Text] [Related]
2. Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid.
Maesaka H; Komiya K; Misugi K; Tada K
Eur J Pediatr; 1976 May; 122(2):159-68. PubMed ID: 817914
[TBL] [Abstract][Full Text] [Related]
3. Thiamine-responsive lactice acidosis in a patient with deficient low-KM pyruvate carboxylase activity in liver.
Brunette MG; Delvin E; Hazel B; Scriver CR
Pediatrics; 1972 Nov; 50(5):702-11. PubMed ID: 4343503
[No Abstract] [Full Text] [Related]
4. Lactic acidosis in three sibs due to defects in both pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes.
Haworth JC; Perry TL; Blass JP; Hansen S; Urquhart N
Pediatrics; 1976 Oct; 58(4):564-72. PubMed ID: 184426
[TBL] [Abstract][Full Text] [Related]
5. [Pyruvate-dehydrogenase deficiency. Lethal course of the disease during infancy (author's transl)].
Wendel U; Przyrembel H; Becker K; Walther B; Berger R; Bremer HJ
Monatsschr Kinderheilkd (1902); 1978 Mar; 126(3):140-7. PubMed ID: 417240
[TBL] [Abstract][Full Text] [Related]
6. Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acid.
Matalon R; Stumpf DA; Michals K; Hart RD; Parks JK; Goodman SI
J Pediatr; 1984 Jan; 104(1):65-9. PubMed ID: 6418873
[TBL] [Abstract][Full Text] [Related]
7. Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings.
Saudubray JM; Marsac C; Cathelineau CL; Besson Leaud M; Leroux JP
Acta Paediatr Scand; 1976 Nov; 65(6):717-24. PubMed ID: 826106
[TBL] [Abstract][Full Text] [Related]
8. Pyruvate carboxylase in human liver. Apparent loss of a component of catalytic activity in a form of lactic acidosis with hypoglycemia.
Delvin E; Scriver CR; Neal JL
Biochem Med; 1974 Jun; 10(2):97-106. PubMed ID: 4364467
[No Abstract] [Full Text] [Related]
9. [Hyperalaninemia-pyruvicemia: chronic lactic acidosis].
Tada K
Nihon Rinsho; 1973 Aug; 31(8):2456-62. PubMed ID: 4797403
[No Abstract] [Full Text] [Related]
10. Subacute necrotising encephalomyelopathy in three siblings.
Gordon N; Marsden HB; Lewis DM
Dev Med Child Neurol; 1974 Feb; 16(1):64-72. PubMed ID: 4813493
[No Abstract] [Full Text] [Related]
11. Lactic acidosis in childhood.
Israels S; Haworth JC; Dunn HG; Applegarth DA
Adv Pediatr; 1976; 22():267-303. PubMed ID: 178159
[TBL] [Abstract][Full Text] [Related]
12. Leigh's encephalomyelopathy: an inborn error of gluconeogenesis.
Hommes FA; Polman HA; Reerink JD
Arch Dis Child; 1968 Aug; 43(230):423-6. PubMed ID: 4873809
[No Abstract] [Full Text] [Related]
13. Subacute necrotizing encephalomyelopathy. Clinical, ultrastructural, biochemical and therapeutic studies in an infant.
Gröbe H; Bassewitz DB; Dominick HC; Pfeiffer RA
Acta Paediatr Scand; 1975 Sep; 64(5):755-62. PubMed ID: 1166795
[TBL] [Abstract][Full Text] [Related]
14. Inherited lactic acidosis: correction of the defect in cultured fibroblasts.
Goodyer PR; Lancaster GA
Pediatr Res; 1984 Nov; 18(11):1144-8. PubMed ID: 6440113
[TBL] [Abstract][Full Text] [Related]
15. Normal activities of hepatic pyruvate dehydrogenase and pyruvate carboxylase in Leigh's syndrome.
Tsuchiyama A; Oyanagi K; Sogawa H; Nakao T; Ogawa K; Fujita S
Tohoku J Exp Med; 1983 Jan; 139(1):67-72. PubMed ID: 6836560
[TBL] [Abstract][Full Text] [Related]
16. The measurement of propionyl-CoA carboxylase and pyruvate carboxylase activity in hair roots: its use in the diagnosis of inherited biotin-dependent enzyme deficiencies.
Wolf B; Raetz H
Clin Chim Acta; 1983 May; 130(1):25-30. PubMed ID: 6851181
[TBL] [Abstract][Full Text] [Related]
17. Secondary metabolic changes in fibroblasts from six patients with hereditary lactic acidosis.
Borud O; Strømme JH
J Inherit Metab Dis; 1978; 1(4):161-2. PubMed ID: 117250
[TBL] [Abstract][Full Text] [Related]
18. [Baker-Winegrad disease (hepatomegaly, hypoglycemia during fasting, hyperlactacidemic metabolic acidosis, hepatic fructose-1-6-diphosphatase deficiency). Presentation of the 1st Italian case and pathogenetic hypothesis].
De Prà M; Laudanna E
Minerva Pediatr; 1978 Dec; 30(24):1973-86. PubMed ID: 224299
[No Abstract] [Full Text] [Related]
19. Molecular analysis of abnormal pyruvate dehydrogenase in a patient with thiamine-responsive congenital lactic acidemia.
Naito E; Ito M; Takeda E; Yokota I; Yoshijima S; Kuroda Y
Pediatr Res; 1994 Sep; 36(3):340-6. PubMed ID: 7808831
[TBL] [Abstract][Full Text] [Related]
20. [Neonatal lactic acidosis caused by severe pyruvate carboxylase deficiency].
Merinero Cortés B; del Valle Martínez J; Pérez-Cerdá Silvestre C; García Muñoz MJ; Cortés Coto MT; García Aparicio J; Sáez Pérez E; Ugarte Pérez M
An Esp Pediatr; 1988 Jul; 29(1):57-60. PubMed ID: 3142324
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
