Mitochondrial myopathy and cardiomyopathy with neurodegenerative features and multiple brain infarcts
- 1 September 1982
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 55 (3) , 351-357
- https://doi.org/10.1016/0022-510x(82)90132-0
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities): Disease entity or a syndrome?Journal of the Neurological Sciences, 1980
- Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome?Annals of Neurology, 1977
- Mitochondrial myopathy with multisystem abnormalities and normal ocular movementsJournal of the Neurological Sciences, 1975
- The Kearns-Shy syndrome: A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skinJournal of the Neurological Sciences, 1973
- Oculocraniosomatic Neuromuscular Disease With "Ragged-Red" FibersArchives of Neurology, 1972
- Ophthalmoplegia PlusArchives of Neurology, 1968
- Familial Myopathy With Abnormal Muscle MitochondriaArchives of Neurology, 1968
- Spongiform encephalopathy with chronic progressive external ophthalmoplegiaNeurology, 1966
- Occurrence of retinal pigmentation, ophthalmoplegia, ataxia, deafness and heart blockThe American Journal of Medicine, 1960
- Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart BlockA.M.A. Archives of Ophthalmology, 1958