Respiratory chain enzyme defects in patients with idiopathic inflammatory myopathy.

Author:

Campos Y,Arenas J,Cabello A,Gomez-Reino J J

Publisher

BMJ

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Rheumatology

Reference12 articles.

1. A new approach to the classification of idiopathic inflammatory myopathy: myositis-specific autoantibodies define useful homogeneous patients groups;A, Love L.; L, Leff R.; D, Fraser D.;Medicine,1991

2. Mitochondrial encephalomyopathies;DiMauro, S.; T, Moraes C.;Arch Neurol,1993

3. The polymyositis and dermatomyositis syndromes;Q, Banker B.; G, Engel A.,1986

4. Polymyositis and dermatomyositis. Part 1;Bohan, A.; B, Peter J.,1975

5. Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA;J, Tristchler H.; F, Andreeta; T, Moraes C.;Neurology,1991

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