Review
doi: 10.1007/BF01799447.
Disorders of the pyruvate dehydrogenase complex
- PMID: 3018357
- DOI: 10.1007/BF01799447
Item in Clipboard
Review
Disorders of the pyruvate dehydrogenase complex
J Inherit Metab Dis.
1986.
Abstract
Pyruvate dehydrogenase deficiency may be a non-specific consequence of many different neurological degenerative disorders. There are also serious methodological problems in estimating the activity of this enzyme complex.
Similar articles
-
Inborn errors of pyruvate metabolism.Biochem Soc Trans. 1983 Dec;11(6):623-6. doi: 10.1042/bst0110623. Biochem Soc Trans. 1983. PMID: 6421637 No abstract available.
-
[E2 and E3 deficiency of pyruvate dehydrogenase complex].Tanpakushitsu Kakusan Koso. 1988 Apr;33(5):666-9. Tanpakushitsu Kakusan Koso. 1988. PMID: 3152088 Japanese. No abstract available.
-
Pyruvate dehydrogenase activity in group N streptococci.Aust J Biol Sci. 1980 Mar;33(1):15-25. Aust J Biol Sci. 1980. PMID: 6772148
-
Mechanism of coupled electron and group transfer in Escherichia coli pyruvate dehydrogenase.Ann N Y Acad Sci. 1982;378:250-64. doi: 10.1111/j.1749-6632.1982.tb31201.x. Ann N Y Acad Sci. 1982. PMID: 6805383 Review. No abstract available.
-
The pyruvate dehydrogenase multi-enzyme complex from Gram-negative bacteria.Biochim Biophys Acta. 1998 Jun 29;1385(2):353-66. doi: 10.1016/s0167-4838(98)00079-x. Biochim Biophys Acta. 1998. PMID: 9655933 Review.
Cited by
-
Neonatal pyruvate dehydrogenase deficiency with lipoate responsive lactic acidaemia and hyperammonaemia.Eur J Pediatr. 1989 Apr;148(6):543-7. doi: 10.1007/BF00441554. Eur J Pediatr. 1989. PMID: 2501097
-
Vitamin-responsive pyruvate dehydrogenase deficiency in a young girl with external ophthalmoplegia, myopathy and lactic acidosis.J Inherit Metab Dis. 1992;15(3):331-4. doi: 10.1007/BF02435969. J Inherit Metab Dis. 1992. PMID: 1405466 No abstract available.
-
Mutation of the E1 alpha subunit of the pyruvate dehydrogenase complex, in relation to heterogeneity.J Inherit Metab Dis. 1989;12(2):97-107. doi: 10.1007/BF01800710. J Inherit Metab Dis. 1989. PMID: 2502681
-
Heterogeneous expression of protein and mRNA in pyruvate dehydrogenase deficiency.Proc Natl Acad Sci U S A. 1988 Oct;85(19):7336-40. doi: 10.1073/pnas.85.19.7336. Proc Natl Acad Sci U S A. 1988. PMID: 3140238 Free PMC article.
-
Mitochondrial myopathies.J Inherit Metab Dis. 1987;10 Suppl 1:113-28. doi: 10.1007/BF01812852. J Inherit Metab Dis. 1987. PMID: 2824920 Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
