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Methods of microphotometric assay of succinate dehydrogenase and cytochrome c oxidase activities for use on human skeletal muscle.
Old SL, Johnson MA. Old SL, et al. Among authors: johnson ma. Histochem J. 1989 Sep-Oct;21(9-10):545-55. doi: 10.1007/BF01753355. Histochem J. 1989. PMID: 2556354
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.
Functional significance of dystrophin positive fibres in Duchenne muscular dystrophy.
Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D. Nicholson LV, et al. Among authors: johnson ma. Arch Dis Child. 1993 May;68(5):632-6. doi: 10.1136/adc.68.5.632. Arch Dis Child. 1993. PMID: 8323331 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
Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy.
Nicholson LV, Johnson MA, Gardner-Medwin D, Bhattacharya S, Harris JB. Nicholson LV, et al. Among authors: johnson ma. Acta Neuropathol. 1990;80(3):239-50. doi: 10.1007/BF00294640. Acta Neuropathol. 1990. PMID: 2205076
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
Influence of electrical stimulation of the tibialis anterior muscle in paraplegic subjects. 2. Morphological and histochemical properties.
Rochester L, Barron MJ, Chandler CS, Sutton RA, Miller S, Johnson MA. Rochester L, et al. Among authors: johnson ma. Paraplegia. 1995 Sep;33(9):514-22. doi: 10.1038/sc.1995.112. Paraplegia. 1995. PMID: 8524604 Clinical Trial.
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