Lipid storage myopathy: A recognizable clinicopathological entity?
- 1 January 1973
- journal article
- research article
- Published by Springer Nature in Acta Neuropathologica
- Vol. 24 (2) , 97-106
- https://doi.org/10.1007/bf00684832
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- Familial “mitochondrial” myopathy: A myopathy associated with disordered oxidative metabolism in muscle fibres Part 1. Clinical, electrophysiological and pathological findingsJournal of the Neurological Sciences, 1972
- A myopathy associated with lipid storageJournal of the Neurological Sciences, 1972
- A Skeletal-Muscle Disorder Associated with Intermittent Symptoms and a Possible Defect of Lipid MetabolismNew England Journal of Medicine, 1970
- MYOPATHY ASSOCIATED WITH ABNORMAL LIPID METABOLISM IN SKELETAL MUSCLEThe Lancet, 1969
- AN IMPROVED METHOD OF FIXATION FOR FORMALIN-SENSITIVE ENZYMES WITH SPECIAL REFERENCE TO MYOSIN ADENOSINE TRIPHOSPHATASEJournal of Histochemistry & Cytochemistry, 1966
- A METHOD FOR THE SIMULTANEOUS DEMONSTRATION OF CHOLINE-CONTAINING PHOSPHOLIPIDS AND NEUTRAL LIPIDS IN TISSUE SECTIONSJournal of Histochemistry & Cytochemistry, 1965
- ARE ACTIVE AND INACTIVE PHOSPHORYLASES HISTOCHEMICALLY DISTINGUISHABLE?Journal of Histochemistry & Cytochemistry, 1963