Ocular Pathology of MELAS Syndrome with Mitochondrial DNA Nucleotide 3243 Point Mutation
- 1 December 1993
- journal article
- case report
- Published by Elsevier in Ophthalmology
- Vol. 100 (12) , 1757-1766
- https://doi.org/10.1016/s0161-6420(13)31404-3
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Mitochondria and Leber's Hereditary Optic NeuropathyAmerican Journal of Ophthalmology, 1990
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- THE CLINICAL FEATURES OF MITOCHONDRIAL MYOPATHYBrain, 1986
- Mitochondrial myopathiesAnnals of Neurology, 1985
- Kearns syndrome: A heterogeneous group of disorders with CPEO, or a nosological entity?Documenta Ophthalmologica, 1982
- MITOCHONDRIAL ENCEPHALOMYOPATHIESBrain, 1982
- PROGRESSIVE EXTERNAL OPHTHALMOPLEGIAActa Ophthalmologica, 1976
- Oculocraniosomatic Neuromuscular Disease With "Ragged-Red" FibersArchives of Neurology, 1972
- Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart BlockA.M.A. Archives of Ophthalmology, 1958