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- Gilbert E. F., Arya S., Chun R. Leigh's necrotizing encephalopathy with pyruvate carboxylase deficiency. Arch Pathol Lab Med. 1983 Apr;107(4):162–166. [PubMed] [Google Scholar]
- Gray F., Louarn F., Gherardi R., Eizenbaum J. F., Marsault C. Adult form of Leigh's disease: a clinico pathological case with CT scan examination. J Neurol Neurosurg Psychiatry. 1984 Nov;47(11):1211–1215. doi: 10.1136/jnnp.47.11.1211. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ho K. L., Piligian J. T., Chason J. L. Adult form of subactute necrotizing encephalomyelopathy. Arch Pathol Lab Med. 1979 Jul;103(7):344–347. [PubMed] [Google Scholar]
- Kesselring J., Miller D. H., Robb S. A., Kendall B. E., Moseley I. F., Kingsley D., du Boulay E. P., McDonald W. I. Acute disseminated encephalomyelitis. MRI findings and the distinction from multiple sclerosis. Brain. 1990 Apr;113(Pt 2):291–302. doi: 10.1093/brain/113.2.291. [DOI] [PubMed] [Google Scholar]
- Kornips H. M., Verhagen W. I., Prick M. J. Acute disseminated encephalomyelitis probably related to a Mycoplasma pneumoniae infection. Clin Neurol Neurosurg. 1993 Mar;95(1):59–63. doi: 10.1016/0303-8467(93)90094-w. [DOI] [PubMed] [Google Scholar]
- Lindquist L., Linné T., Hansson L. O., Kalin M., Axelsson G. Value of cerebrospinal fluid analysis in the differential diagnosis of meningitis: a study in 710 patients with suspected central nervous system infection. Eur J Clin Microbiol Infect Dis. 1988 Jun;7(3):374–380. doi: 10.1007/BF01962340. [DOI] [PubMed] [Google Scholar]
- Logigian E. L., Kaplan R. F., Steere A. C. Chronic neurologic manifestations of Lyme disease. N Engl J Med. 1990 Nov 22;323(21):1438–1444. doi: 10.1056/NEJM199011223232102. [DOI] [PubMed] [Google Scholar]
- Sipe J. C. Leigh's syndrome: the adult form of subacute necrotizing encephalomyelopathy with predilection for the brainstem. Neurology. 1973 Oct;23(10):1030–1038. doi: 10.1212/wnl.23.10.1030. [DOI] [PubMed] [Google Scholar]
- Sweeney M. G., Hammans S. R., Duchen L. W., Cooper J. M., Schapira A. H., Kennedy C. R., Jacobs J. M., Youl B. D., Morgan-Hughes J. A., Harding A. E. Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsy. J Neurol Sci. 1994 Jan;121(1):57–65. doi: 10.1016/0022-510x(94)90157-0. [DOI] [PubMed] [Google Scholar]
- Van Coster R., Lombres A., De Vivo D. C., Chi T. L., Dodson W. E., Rothman S., Orrechio E. J., Grover W., Berry G. T., Schwartz J. F. Cytochrome c oxidase-associated Leigh syndrome: phenotypic features and pathogenetic speculations. J Neurol Sci. 1991 Jul;104(1):97–111. doi: 10.1016/0022-510x(91)90222-s. [DOI] [PubMed] [Google Scholar]





