Weakness associated with the pathological presence of lipid in skeletal muscle: a detailed study of a patient with carnitine deficiencey.

Author:

Isaacs H,Heffron J J,Badenhorst M,Pickering A

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference28 articles.

1. A disorder of muscle lipid metabolism and myoglobinuria. Absence of carnitine palmityl transferase;Bank, W.J.; Di Mauro, S.; Bonilla, E.; Capuzzi, D.M.; Rowland, L.P.;New England Journal of Medicine,1975

2. Myopathy associated with abnormal lipid metabolism in skeletal muscle;Bradley, W.G.; Hudgson, P.; Gardner-Medwin, D.;Lancet,1969

3. A myopathy associated with lipid storage;Bradley, W.G.; Jenkinson, M.; Park, D.L.;Journal of the Neurological Sciences,1972

4. Carnitine and the twins;Bressler, R.;(Editorial). New EnglandJournalofMedicine,1970

5. Neutral-lipid disease: a new disorder of lipid metabolism;Chanarin, I.; Patel, A.; Slavin, G.; Wills, E.J.; M., Andrews T.; Stewart, G.;British Medical Journal,1975

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