172 related articles for article (PubMed ID: 6434849)
21. Five patients with a biotin-responsive defect in holocarboxylase formation: evaluation of responsiveness to biotin therapy in vivo and comparative biochemical studies in vitro.
Suormala T; Fowler B; Duran M; Burtscher A; Fuchshuber A; Tratzmüller R; Lenze MJ; Raab K; Baur B; Wick H; Baumgartner R
Pediatr Res; 1997 May; 41(5):666-73. PubMed ID: 9128289
[TBL] [Abstract][Full Text] [Related]
22. Lactic acidosis in biotin-responsive multiple carboxylase deficiency caused by holocarboxylase synthetase deficiency of early and late onset.
Sherwood WG; Saunders M; Robinson BH; Brewster T; Gravel RA
J Pediatr; 1982 Oct; 101(4):546-50. PubMed ID: 6811711
[TBL] [Abstract][Full Text] [Related]
23. Studies on pyruvate carboxylase, pyruvate decarboxylase and lipoamide dehydrogenase in subacute necrotizing encephalomyelopathy.
Hansen TL; Christensen E; Brandt NJ
Acta Paediatr Scand; 1982 Mar; 71(2):263-7. PubMed ID: 6897146
[TBL] [Abstract][Full Text] [Related]
24. Dietary treatment and biochemical studies on a neonatal case of propionyl-CoA carboxylase deficiency.
DelValle JA; Merinero B; Jiménez A; García MJ; Ugarte M; Omeñaca F; Neustadt G; Quero J
J Inherit Metab Dis; 1982; 5(2):121-4. PubMed ID: 6820422
[TBL] [Abstract][Full Text] [Related]
25. [Differential diagnosis of the symptom of lactic acidosis in childhood].
Koepp P
Monatsschr Kinderheilkd; 1984 May; 132(5):264-7. PubMed ID: 6087128
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Inborn errors of pyruvate metabolism.
Robinson BH
Biochem Soc Trans; 1983 Dec; 11(6):623-6. PubMed ID: 6421637
[No Abstract] [Full Text] [Related]
28. Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase.
Tada K; Takada G; Omura K; Itokawa Y
Eur J Pediatr; 1978 Jan; 127(2):141-7. PubMed ID: 203466
[TBL] [Abstract][Full Text] [Related]
29. Biotin-dependent carboxylase deficiencies (propionyl-CoA and pyruvate carboxylases).
Gravel RA; Robinson BH
Ann N Y Acad Sci; 1985; 447():225-34. PubMed ID: 3925855
[No Abstract] [Full Text] [Related]
30. Absence of pyruvate decarboxylase activity in man: a cause of congenital lactic acidosis.
Farrell DF; Clark AF; Scott CR; Wennberg RP
Science; 1975 Mar; 187(4181):1082-4. PubMed ID: 803713
[TBL] [Abstract][Full Text] [Related]
31. A case of pyruvate carboxylase deficiency with later prenatal diagnosis of an unaffected sibling.
Tsuchiyama A; Oyanagi K; Hirano S; Tachi N; Sogawa H; Wagatsuma K; Nakao T; Tsugawa S; Kawamura Y
J Inherit Metab Dis; 1983; 6(3):85-8. PubMed ID: 6422150
[TBL] [Abstract][Full Text] [Related]
32. Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiency.
Coude FX; Ogier H; Marsac C; Munnich A; Charpentier C; Saudubray JM
Pediatrics; 1981 Dec; 68(6):914. PubMed ID: 6798542
[No Abstract] [Full Text] [Related]
33. [Enzymopathic congenital hyperlactacidemia].
Leroux JP; Marsac C; Saudubray JM
Ann Biol Clin (Paris); 1976; 34(2):151-9. PubMed ID: 184725
[TBL] [Abstract][Full Text] [Related]
34. Congenital lactic acidosis associated with pyruvate carboxylase deficiency.
Sagy M; Barzilay Z; Barash V; Oren M; Vardi P; Cohen BE; Gutman A
Isr J Med Sci; 1981 Dec; 17(12):1159-63. PubMed ID: 6799424
[TBL] [Abstract][Full Text] [Related]
35. Fatty-acid-responsive alopecia in multiple carboxylase deficiency.
Munnich A; Saudubray JM; Coude FX; Charpentier C; Saurat JH; Frezal J
Lancet; 1980 May; 1(8177):1080-1. PubMed ID: 6103410
[No Abstract] [Full Text] [Related]
36. [Propionic acidemia].
Ohura T
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):276-9. PubMed ID: 9590046
[No Abstract] [Full Text] [Related]
37. Multiple carboxylase deficiency: clinical and biochemical improvement following neonatal biotin treatment.
Wolf B; Hsia YE; Sweetman L; Feldman G; Boychuk RB; Bart RD; Crowell DH; Di Mauro RM; Nyhan WL
Pediatrics; 1981 Jul; 68(1):113-8. PubMed ID: 6787561
[TBL] [Abstract][Full Text] [Related]
38. Pyruvate decarboxylase deficiency in subacute necrotizing encephalomyelopathy.
Evans OB
Arch Neurol; 1981 Aug; 38(8):515-9. PubMed ID: 7247788
[TBL] [Abstract][Full Text] [Related]
39. Hyperalaninemia with pyruvicemia due to pyruvate carboxylase deficiency of the liver.
Yoshida T; Tada K; Konno T; Arakawa T
Tohoku J Exp Med; 1969 Oct; 99(2):121-8. PubMed ID: 5358431
[No Abstract] [Full Text] [Related]
40. A patient with pyruvate carboxylase deficiency in the liver: treatment with aspartic acid and thiamine.
Baal MG; Gabreëls FJ; Renier WO; Hommes FA; Gijsbers TH; Lamers KJ; Kok JC
Dev Med Child Neurol; 1981 Aug; 23(4):521-30. PubMed ID: 6791975
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
