Electrophysiological findings including single fibre EMG in a family with mitochondrial myopathy
- 1 February 1982
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 53 (2), 397-410
- https://doi.org/10.1016/0022-510x(82)90021-1
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Mitochondrial myopathyJournal of the Neurological Sciences, 1981
- Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red FibersArchives of Neurology, 1978
- Myopathies with abnormal mitochondria: A clinicopathologic classificationMuscle & Nerve, 1978
- Further studies of mitochondrial and lipid storage myopathiesJournal of the Neurological Sciences, 1978
- Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome?Annals of Neurology, 1977
- Relationship of spontaneous fibrillation potentials to muscle fibre segmentation in human muscular dystrophyNature, 1975
- Electromyographical Studies of Free Autogenous Muscle Transplants in ManScandinavian Journal of Plastic and Reconstructive Surgery, 1974
- Myopathie distale et congénitale, avec hypertrophie des molletsJournal of the Neurological Sciences, 1972
- 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
- Oculocraniosomatic Neuromuscular Disease With "Ragged-Red" FibersArchives of Neurology, 1972