Margaret A. Johnson

发表

Data on the distribution of fibre types in thirty-six human muscles. An autopsy study.

M. Johnson, J. Polgár, D. Weightman, 1973, Journal of the neurological sciences.

Skeletal Muscle Involvement in Systemic Sclerosis *

E. Bywaters, R. Bluestone, J. M. Thompson, 1969, Annals of the rheumatic diseases.

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis.

K. Bushby, J. D. den Dunnen, M. Johnson, 1993, Journal of medical genetics.

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy.

R. Waterston, K. Fischbeck, L. Kunkel, 1988, The New England journal of medicine.

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients.

K. Bushby, J. D. den Dunnen, M. Johnson, 1993, Journal of medical genetics.

Dopamine and nicotinic receptor binding and the levels of dopamine and homovanillic acid in human brain related to tobacco use

E. Perry, E. Marshall, R. Perry, 1998, Neuroscience.

Data on fibre size in thirty-six human muscles. An autopsy study.

M. Johnson, J. Polgár, D. Weightman, 1973, Journal of the neurological sciences.

Convergent cholinergic activities in aging and Alzheimer's disease

E. Perry, P. Ince, J. Kerwin, 1992, Neurobiology of Aging.

A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle.

D. Turnbull, M. Johnson, L. Bindoff, 1997, American journal of human genetics.

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

D. Turnbull, M. Johnson, L. Bindoff, 1995, Brain : a journal of neurology.

A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis

D. Turnbull, M. Johnson, P. Chinnery, 1997, Annals of neurology.

The epidemiology of pathogenic mitochondrial DNA mutations

D. Turnbull, M. Johnson, P. Chinnery, 2000, Annals of neurology.

An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.

D. Turnbull, I. Nelson, N. Wood, 1999, American journal of human genetics.

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups.

K. Bushby, J. D. den Dunnen, M. Johnson, 1993, Journal of medical genetics.

Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age

D. Turnbull, M. Johnson, G. Borthwick, 2001, Neurobiology of Aging.

Paraplegin gene analysis in hereditary spastic paraparesis (HSP) pedigrees in northeast England

D. Turnbull, M. Johnson, P. Shaw, 2001, Neurology.

Skeletal Muscle Involvement in Systemic Sclerosis *

E. Bywaters, R. Bluestone, J. Thompson, 1969, Annals of the rheumatic diseases.

Neuropathological and Histochemical Changes in a Multiple Mitochondrial DNA Deletion Disorder

D. Turnbull, M. Johnson, P. Chinnery, 2000, Journal of neuropathology and experimental neurology.