Symmetric lesions of the subthalamic nuclei in mitochondrial encephalopathies: an almost distinctive Mark of Leigh disease with COX deficiency
- PMID: 7502989
- PMCID: PMC8337772
Symmetric lesions of the subthalamic nuclei in mitochondrial encephalopathies: an almost distinctive Mark of Leigh disease with COX deficiency
Comment on
-
Hemiballismus.AJNR Am J Neuroradiol. 1994 Aug;15(7):1377-82. AJNR Am J Neuroradiol. 1994. PMID: 7976952 Free PMC article. No abstract available.
Similar articles
-
Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findings.AJNR Am J Neuroradiol. 2003 Jun-Jul;24(6):1188-91. AJNR Am J Neuroradiol. 2003. PMID: 12812953 Free PMC article.
-
Mitochondrial diseases in children: neuroradiological and clinical features in 17 patients.Neuroradiology. 1999 Dec;41(12):920-8. doi: 10.1007/s002340050868. Neuroradiology. 1999. PMID: 10639669
-
[Adult Leigh syndrome. A rare differential diagnosis of central respiratory insufficiency].Nervenarzt. 1995 Feb;66(2):144-9. Nervenarzt. 1995. PMID: 7715756 German.
-
[Leigh syndrome in the adult].Arch Neurobiol (Madr). 1986 May-Jun;49(3):129-35. Arch Neurobiol (Madr). 1986. PMID: 3017252 Review. Spanish. No abstract available.
-
Biochemical defects and genetic abnormalities in cytochrome c oxidase of patients with Leigh syndrome.Biofactors. 1998;7(3):273-6. doi: 10.1002/biof.5520070326. Biofactors. 1998. PMID: 9568266 Review. No abstract available.
Cited by
-
Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findings.AJNR Am J Neuroradiol. 2003 Jun-Jul;24(6):1188-91. AJNR Am J Neuroradiol. 2003. PMID: 12812953 Free PMC article.
-
A rare mitochondrial disorder: Leigh syndrome--a case report.Ital J Pediatr. 2010 Sep 15;36:62. doi: 10.1186/1824-7288-36-62. Ital J Pediatr. 2010. PMID: 20843336 Free PMC article.
-
Leigh syndrome: MRI findings in two children.Biomed Imaging Interv J. 2010 Jan-Mar;6(1):e6. doi: 10.2349/biij.6.1.e6. Epub 2010 Jan 1. Biomed Imaging Interv J. 2010. PMID: 21611066 Free PMC article.
-
Radio-imaging for detecting congenitally defective metabolic pathways: A review.Australas Med J. 2011;4(9):480-4. doi: 10.4066/AMJ.2011.822. Epub 2011 Sep 30. Australas Med J. 2011. PMID: 23393538 Free PMC article.
-
Pediatric neurodegenerative white matter processes: leukodystrophies and beyond.Pediatr Radiol. 2008 Jul;38(7):729-49. doi: 10.1007/s00247-008-0817-x. Epub 2008 Apr 30. Pediatr Radiol. 2008. PMID: 18446335 Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical