Bindoff LA - Search Results

1

Familial intermittent ataxia due to a defect of the E1 component of pyruvate dehydrogenase complex.

Bindoff LA, Birch-Machin MA, Farnsworth L, Gardner-Medwin D, Lindsay JG, Turnbull DM. Bindoff LA, et al. J Neurol Sci. 1989 Nov;93(2-3):311-8. doi: 10.1016/0022-510x(89)90200-1. J Neurol Sci. 1989. PMID: 2592988

2

The sequence of the flavoprotein subunit of bovine heart succinate dehydrogenase.

Birch-Machin MA, Farnsworth L, Ackrell BA, Cochran B, Jackson S, Bindoff LA, Aitken A, Diamond AG, Turnbull DM. Birch-Machin MA, et al. Among authors: bindoff la. J Biol Chem. 1992 Jun 5;267(16):11553-8. J Biol Chem. 1992. PMID: 1375942 Free article.

3

Combined enzyme defect of mitochondrial fatty acid oxidation.

Jackson S, Kler RS, Bartlett K, Briggs H, Bindoff LA, Pourfarzam M, Gardner-Medwin D, Turnbull DM. Jackson S, et al. Among authors: bindoff la. J Clin Invest. 1992 Oct;90(4):1219-25. doi: 10.1172/JCI115983. J Clin Invest. 1992. PMID: 1401059 Free PMC article.

4

Mitochondrial gene segregation in mammals: is the bottleneck always narrow?

Howell N, Halvorson S, Kubacka I, McCullough DA, Bindoff LA, Turnbull DM. Howell N, et al. Among authors: bindoff la. Hum Genet. 1992 Sep-Oct;90(1-2):117-20. doi: 10.1007/BF00210753. Hum Genet. 1992. PMID: 1427765

5

Combined defect of long-chain 3-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase and 3-oxoacyl-CoA thiolase.

Jackson S, Kler RS, Bartlett K, Pourfarzam M, Aynsley-Green A, Bindoff LA, Turnbull DM. Jackson S, et al. Among authors: bindoff la. Prog Clin Biol Res. 1992;375:327-37. Prog Clin Biol Res. 1992. PMID: 1438378 No abstract available.

6

Leigh syndrome associated with a deficiency of the pyruvate dehydrogenase complex: results of treatment with a ketogenic diet.

Wijburg FA, Barth PG, Bindoff LA, Birch-Machin MA, van der Blij JF, Ruitenbeek W, Turnbull DM, Schutgens RB. Wijburg FA, et al. Among authors: bindoff la. Neuropediatrics. 1992 Jun;23(3):147-52. doi: 10.1055/s-2008-1071331. Neuropediatrics. 1992. PMID: 1641082

7

Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular study.

Bindoff LA, Desnuelle C, Birch-Machin MA, Pellissier JF, Serratrice G, Dravet C, Bureau M, Howell N, Turnbull DM. Bindoff LA, et al. J Neurol Sci. 1991 Mar;102(1):17-24. doi: 10.1016/0022-510x(91)90088-o. J Neurol Sci. 1991. PMID: 1649912 Review.

8

Respiratory chain abnormalities in skeletal muscle from patients with Parkinson's disease.

Bindoff LA, Birch-Machin MA, Cartlidge NE, Parker WD Jr, Turnbull DM. Bindoff LA, et al. J Neurol Sci. 1991 Aug;104(2):203-8. doi: 10.1016/0022-510x(91)90311-t. J Neurol Sci. 1991. PMID: 1658241

9

Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation.

Kler RS, Jackson S, Bartlett K, Bindoff LA, Eaton S, Pourfarzam M, Frerman FE, Goodman SI, Watmough NJ, Turnbull DM. Kler RS, et al. Among authors: bindoff la. J Biol Chem. 1991 Dec 5;266(34):22932-8. J Biol Chem. 1991. PMID: 1744086 Free article.

10

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.

Howell N, Bindoff LA, McCullough DA, Kubacka I, Poulton J, Mackey D, Taylor L, Turnbull DM. Howell N, et al. Among authors: bindoff la. Am J Hum Genet. 1991 Nov;49(5):939-50. Am J Hum Genet. 1991. PMID: 1928099 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

229 results

Search Page

Filters