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5. Pyruvate carboxylase and phosphoenopyruvate carboxykinase in cultured human fibroblasts. Raghunathan R; Russell JD; Arinze IJ J Cell Physiol; 1977 Aug; 92(2):285-92. PubMed ID: 881436 [TBL] [Abstract][Full Text] [Related]
6. Carrier detection of pyruvate carboxylase deficiency in fibroblasts and lymphocytes. Atkin BM Pediatr Res; 1979 Oct; 13(10):1101-4. PubMed ID: 116187 [TBL] [Abstract][Full Text] [Related]
7. Pyruvate dehydrogenase, lipoamide dehydrogenase and citrate synthase activity in fibroblasts from patients with Friedreich's and Charlevoix-Saguenay ataxia. Melancon SB; Potier M; Dallaire L; Rollin P; Fontaine G; Grenier B Can J Neurol Sci; 1979 May; 6(2):241-2. PubMed ID: 487317 [TBL] [Abstract][Full Text] [Related]
8. Normal pyruvate oxidation in Friedreich ataxia and Charcot-Marie-Tooth disease fibroblasts. Wilson WG Clin Chim Acta; 1985 Dec; 153(3):233-9. PubMed ID: 4075529 [TBL] [Abstract][Full Text] [Related]
9. Pyruvate-dehydrogenase complex in ataxic patients: enzyme deficiency in ataxic encephalopathy plus lactic acidosis and normal activity in Friedreich ataxia. Uziel G; Bottacchi E; Moschen G; Giovanardi-Rossi P; Cardace G; Di Donato S Ital J Neurol Sci; 1982 Dec; 3(4):317-21. PubMed ID: 6820014 [TBL] [Abstract][Full Text] [Related]
10. Friedreich ataxia. II. Normal kinetics of lipoamide dehydrogenase. Stumpf DA; Parks JK Neurology; 1979 Jun; 29(6):820-6. PubMed ID: 221857 [TBL] [Abstract][Full Text] [Related]
11. [Proceedings: Infantile cerebral poliodystrophy (Alper's disease) in an infant with hyperlactacidemia and hepatic pyruvate carboxylase]. David M; Baltassat P; Dinjon B; Lauras B; De Villard R; Tommasi M; Gilly J Arch Fr Pediatr; 1975; 32(6):580. PubMed ID: 1180638 [No Abstract] [Full Text] [Related]
12. Studies on pyruvate carboxylase from cultured human fibroblasts and amniotic fluid cells. Hansen TL; Christensen E J Inherit Metab Dis; 1980; 2(2):23-8. PubMed ID: 6796757 [TBL] [Abstract][Full Text] [Related]
13. The inherited ataxias. Stumpf DA Neurol Clin; 1985 Feb; 3(1):47-57. PubMed ID: 3921817 [TBL] [Abstract][Full Text] [Related]
14. Normal pyruvate dehydrogenase complex activity in patients with Friedreich's ataxia. Constantopoulos G; Chang CS; Barranger JA Ann Neurol; 1980 Dec; 8(6):636-9. PubMed ID: 7212654 [No Abstract] [Full Text] [Related]
15. Pyruvate carboxylase activity in the heart and skeletal muscles of the rat. Evidence for a stimulating effect of exercise. Lancha AH; Recco MB; Curi R Biochem Mol Biol Int; 1994 Mar; 32(3):483-9. PubMed ID: 8032315 [TBL] [Abstract][Full Text] [Related]
16. Friedreich ataxia: III. Mitochondrial malic enzyme deficiency. Stumpf DA; Parks JK; Eguren LA; Haas R Neurology; 1982 Mar; 32(3):221-7. PubMed ID: 7199631 [TBL] [Abstract][Full Text] [Related]
18. Friedreich's ataxia: I. Normal pyruvate dehydrogenase complex activity in platelets. Stumpf DA; Parks JK Ann Neurol; 1978 Oct; 4(4):366-8. PubMed ID: 727741 [No Abstract] [Full Text] [Related]
19. [Alpers' infantile cerebral poliodystrophy. A case with abnormal hepatic pyruvate carboxylase]. Tommasi M; Jouvet-Telinge A; Kopp N; Pialat J; Gilly J Ann Anat Pathol (Paris); 1977; 22(4):337-42. PubMed ID: 615502 [TBL] [Abstract][Full Text] [Related]
20. Neonatal pyruvate carboxylase deficiency with renal tubular acidosis and cystinuria. Oizumi J; Shaw KN; Giudici TA; Carter M; Donnell GN; Ng WG J Inherit Metab Dis; 1983; 6(3):89-94. PubMed ID: 6422151 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]