Johnson MA - Search Results

1

Munsat TL, Hudgson P, Johnson MA. Munsat TL, et al. Among authors: johnson ma. Neurology. 1977 Aug;27(8):772-82. doi: 10.1212/wnl.27.8.772. Neurology. 1977. PMID: 560648

2

A novel autosomal dominant distal myopathy with early respiratory failure: clinico-pathologic characteristics and exclusion of linkage to candidate genetic loci.

Chinnery PF, Johnson MA, Walls TJ, Gibson GJ, Fawcett PR, Jamieson S, Fulthorpe JJ, Cullen M, Hudgson P, Bushby KM. Chinnery PF, et al. Among authors: johnson ma. Ann Neurol. 2001 Apr;49(4):443-52. Ann Neurol. 2001. PMID: 11310621

3

Lipid storage myopathy: a recognizable clinicopathological entity?

Johnson MA, Fulthorpe JJ, Hudgson P. Johnson MA, et al. Acta Neuropathol. 1973 Apr 18;24(2):97-106. doi: 10.1007/BF00684832. Acta Neuropathol. 1973. PMID: 4715530 No abstract available.

4

Mitochondrial myopathies. A clinico-pathological study of cases with and without extra-ocular muscle involvement.

Mechler F, Mastaglia FL, Serena M, Jenkison M, Johnson MA, Fawcett PR, Hudgson P, Walton JN. Mechler F, et al. Among authors: johnson ma. Aust N Z J Med. 1986 Apr;16(2):185-92. doi: 10.1111/j.1445-5994.1986.tb01146.x. Aust N Z J Med. 1986. PMID: 3463270

5

A sartorial challenge.

Reading PJ, Hudgson P, Johnson MA, Jenkins A. Reading PJ, et al. Among authors: johnson ma. Lancet. 1999 Sep 18;354(9183):996. doi: 10.1016/s0140-6736(99)05342-8. Lancet. 1999. PMID: 10501363 No abstract available.

6

Improved diagnosis of Becker muscular dystrophy by dystrophin testing.

Hoffman EP, Kunkel LM, Angelini C, Clarke A, Johnson M, Harris JB. Hoffman EP, et al. Neurology. 1989 Aug;39(8):1011-7. doi: 10.1212/wnl.39.8.1011. Neurology. 1989. PMID: 2668783

7

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

8

Emetine myopathy in the rat.

Bradley WG, Fewings JD, Harris JB, Johnson MA. Bradley WG, et al. Among authors: johnson ma. Br J Pharmacol. 1976 May;57(1):29-41. doi: 10.1111/j.1476-5381.1976.tb07653.x. Br J Pharmacol. 1976. PMID: 1276539 Free PMC article.

9

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

10

Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy.

Turnbull DM, Bartlett K, Eyre JA, Gardner-Medwin D, Johnson MA, Fisher J, Watmough NJ. Turnbull DM, et al. Among authors: johnson ma. Dev Med Child Neurol. 1988 Oct;30(5):667-72. doi: 10.1111/j.1469-8749.1988.tb04806.x. Dev Med Child Neurol. 1988. PMID: 3229565

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