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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
A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndrome.
Maniura-Weber K, Taylor RW, Johnson MA, Chrzanowska-Lightowlers Z, Morris AA, Charlton CP, Turnbull DM, Bindoff LA. Maniura-Weber K, et al. Among authors: johnson ma. Eur J Hum Genet. 2004 Jun;12(6):509-12. doi: 10.1038/sj.ejhg.5201185. Eur J Hum Genet. 2004. PMID: 15054399
The distribution of mitochondrial activity in relation to optic nerve structure.
Bristow EA, Griffiths PG, Andrews RM, Johnson MA, Turnbull DM. Bristow EA, et al. Among authors: johnson ma. Arch Ophthalmol. 2002 Jun;120(6):791-6. doi: 10.1001/archopht.120.6.791. Arch Ophthalmol. 2002. PMID: 12049585
The length of cytochrome c oxidase-negative segments in muscle fibres in patients with mtDNA myopathy.
Elson JL, Samuels DC, Johnson MA, Turnbull DM, Chinnery PF. Elson JL, et al. Among authors: johnson ma. Neuromuscul Disord. 2002 Nov;12(9):858-64. doi: 10.1016/s0960-8966(02)00047-0. Neuromuscul Disord. 2002. PMID: 12398838 Clinical Trial.
Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene.
Bidooki S, Jackson MJ, Johnson MA, Chrzanowska-Lightowlers ZM, Taylor RW, Venables G, Lightowlers RN, Turnbull DM, Bindoff LA. Bidooki S, et al. Among authors: johnson ma. Neuromuscul Disord. 2004 Jul;14(7):417-20. doi: 10.1016/j.nmd.2004.03.004. Neuromuscul Disord. 2004. PMID: 15210164
The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities.
Bushby KM, Gardner-Medwin D, Nicholson LV, Johnson MA, Haggerty ID, Cleghorn NJ, Harris JB, Bhattacharya SS. Bushby KM, et al. Among authors: johnson ma. J Neurol. 1993 Feb;240(2):105-12. doi: 10.1007/BF00858726. J Neurol. 1993. PMID: 8437017
Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups.
Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E, et al. Nicholson LV, et al. Among authors: johnson ma. J Med Genet. 1993 Sep;30(9):728-36. doi: 10.1136/jmg.30.9.728. J Med Genet. 1993. PMID: 8411067 Free PMC article.
Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophy.
Nicholson LV, Davison K, Johnson MA, Slater CR, Young C, Bhattacharya S, Gardner-Medwin D, Harris JB. Nicholson LV, et al. Among authors: johnson ma. J Neurol Sci. 1989 Dec;94(1-3):137-46. doi: 10.1016/0022-510x(89)90224-4. J Neurol Sci. 1989. PMID: 2693618
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
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
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