Johnson MA - Search Results

1

Absence of immunoreactive enzyme protein in short-chain acylcoenzyme A dehydrogenase deficiency.

Farnsworth L, Shepherd IM, Johnson MA, Bindoff LA, Turnbull DM. Farnsworth L, et al. Among authors: johnson ma. Ann Neurol. 1990 Nov;28(5):717-20. doi: 10.1002/ana.410280520. Ann Neurol. 1990. PMID: 2260861

2

Mitochondrial enzyme-deficient hippocampal neurons and choroidal cells in AD.

Cottrell DA, Blakely EL, Johnson MA, Ince PG, Turnbull DM. Cottrell DA, et al. Among authors: johnson ma. Neurology. 2001 Jul 24;57(2):260-4. doi: 10.1212/wnl.57.2.260. Neurology. 2001. PMID: 11468310

3

Lipid storage myopathy associated with low acyl-CoA dehydrogenase activities.

Turnbull DM, Shepherd IM, Ashworth B, Bartlett K, Johnson MA, Cullen MJ, Jackson S, Sherratt HS. Turnbull DM, et al. Among authors: johnson ma. Brain. 1988 Aug;111 ( Pt 4):815-28. doi: 10.1093/brain/111.4.815. Brain. 1988. PMID: 3042086

4

Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patients.

Jackson MJ, Schaefer JA, Johnson MA, Morris AA, Turnbull DM, Bindoff LA. Jackson MJ, et al. Among authors: johnson ma. Brain. 1995 Apr;118 ( Pt 2):339-57. doi: 10.1093/brain/118.2.339. Brain. 1995. PMID: 7735877

5

Cytochrome c oxidase activity in single muscle fibers: assay techniques and diagnostic applications.

Johnson MA, Bindoff LA, Turnbull DM. Johnson MA, et al. Ann Neurol. 1993 Jan;33(1):28-35. doi: 10.1002/ana.410330106. Ann Neurol. 1993. PMID: 8388186

6

A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis.

Chinnery PF, Johnson MA, Taylor RW, Lightowlers RN, Turnbull DM. Chinnery PF, et al. Among authors: johnson ma. Ann Neurol. 1997 Mar;41(3):408-10. doi: 10.1002/ana.410410319. Ann Neurol. 1997. PMID: 9066365

7

Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle.

Brierley EJ, Johnson MA, Lightowlers RN, James OF, Turnbull DM. Brierley EJ, et al. Among authors: johnson ma. Ann Neurol. 1998 Feb;43(2):217-23. doi: 10.1002/ana.410430212. Ann Neurol. 1998. PMID: 9485063

8

Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell death.

Borthwick GM, Johnson MA, Ince PG, Shaw PJ, Turnbull DM. Borthwick GM, et al. Among authors: johnson ma. Ann Neurol. 1999 Nov;46(5):787-90. doi: 10.1002/1531-8249(199911)46:5<787::aid-ana17>3.0.co;2-8. Ann Neurol. 1999. PMID: 10553999

9

The epidemiology of pathogenic mitochondrial DNA mutations.

Chinnery PF, Johnson MA, Wardell TM, Singh-Kler R, Hayes C, Brown DT, Taylor RW, Bindoff LA, Turnbull DM. Chinnery PF, et al. Among authors: johnson ma. Ann Neurol. 2000 Aug;48(2):188-93. Ann Neurol. 2000. PMID: 10939569

10

Cytochrome oxidase deficiency: immunological studies of skeletal muscle mitochondrial fractions.

Shepherd IM, Birch-Machin MA, Johnson MA, Sherratt HS, Aynsley-Green A, Droste M, Kadenbach B, Stephenson JB, King MD, Dick DJ, et al. Shepherd IM, et al. Among authors: johnson ma. J Neurol Sci. 1988 Nov;87(2-3):265-74. doi: 10.1016/0022-510x(88)90251-1. J Neurol Sci. 1988. PMID: 2850350

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