A case of the Kearns - Shy syndrome
- 31 December 1979
- journal article
- case report
- Published by Elsevier in Clinical Neurology and Neurosurgery
- Vol. 81 (1) , 45-52
- https://doi.org/10.1016/s0303-8467(79)80006-2
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Experimental mitochondrial myopathy produced by in vivo uncoupling of oxidative phosphorylationJournal of the Neurological Sciences, 1975
- CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, PIGMENTARY RETINOPATHY, AND HEART BLOCK (KEARNS‐SAYRE SYNDROME)Acta Ophthalmologica, 1975
- The Kearns-Shy syndrome: A multisystem disease with mitochondrial abnormality demonstrated in skeletal muscle and skinJournal of the Neurological Sciences, 1973
- Ophthalmoplegia plus with morphological and chemical studies of cerebellar and muscle tissueJournal of the Neurological Sciences, 1973
- 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 generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndromeThe American Journal of Medicine, 1967
- A generalized disorder of nervous system, skeletal muscle and heart resembling Refsum's disease and Hurler's syndromeThe American Journal of Medicine, 1967
- CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA AND MUSCULAR DYSTROPHYActa Ophthalmologica, 1963
- Occurrence of retinal pigmentation, ophthalmoplegia, ataxia, deafness and heart blockThe American Journal of Medicine, 1960
- PROGRESSIVE DYSTROPHY OF THE EXTERNAL OCULAR MUSCLESBrain, 1951