Neuro-ophthalmologic Manifestations of Mitochondrial DNA Disorders: Chronic Progressive External Ophthalmoplegia, Kearns-Sayre Syndrome, and Leber’s Hereditary Optic Neuropathy
- 1 February 1991
- journal article
- review article
- Published by Elsevier in Neurologic Clinics
- Vol. 9 (1) , 147-161
- https://doi.org/10.1016/s0733-8619(18)30308-6
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNAGenomics, 1989
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- IDENTICAL MITOCHONDRIAL DNA DELETION IN BLOOD AND MUSCLEThe Lancet, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988
- Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathyBiochemical and Biophysical Research Communications, 1988
- Cardiac involvement in the Kearns-Sayre syndromeThe American Journal of Cardiology, 1987
- MITOCHONDRIAL MYOPATHIES. A CLINICO‐PATHOLOGICAL STUDY OF CASES WITH AND WITHOUT EXTRA‐OCULAR MUSCLE INVOLVEMENTAustralian and New Zealand Journal of Medicine, 1986
- Retinal pathology in the Kearns-Sayre syndrome.British Journal of Ophthalmology, 1985
- Mitochondrial Cytopathy or Leigh's Syndrome?Neuropediatrics, 1982
- Myocardial ultrastructure and the development of atrioventricular block in Kearns-Sayre syndrome.Circulation, 1981