"Mitochondrial myopathy" or mitochondrial disease? EEG, ERG, VEP studies in 13 children.

Author:

Harden A,Pampiglione G,Battaglia A

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference30 articles.

1. A case of severe hypermetabolism of nonthyroid origin with defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical and morphological study;lLuft R; D, Ikkos; G, Palmieri; L, Ernster; B, Afzelius;J ofClin Inv,1962

2. Severe hypermetabolism with primary abnormality of skeletal muscle mitochondria: functional and therapeutic effects of chloramphenicol treatment;Haydar, N.A.; Conn, H.L.; Afifi, A.; Wakid, N.; Ballas, S.; Fawaz, K.;Ann Intern Med; Luft's disease: further biochemical and ultrastructural studies of skeletal muscle in the second case,1971

3. Oculocraniosomatic neuromuscular disease with "ragged red";Olson, W.; Engel, W.K.; Walsh, G.O.; Einaugler, R.;fibers. Arch Neurol,1972

4. Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissue;Schneck, L.; Adachi, M.; Briet, P.; Wolintz, A.; Volk, B.W.;J Neurol Sci,1973

5. Atypical muscle mitochondria in oculoskeletal myopathy;Morgan-Hughes, J.A.; Mair, W.G.P.;Brain,1973

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