Comment on

• Thiamine triphosphate levels and histopathology. Correlation in Leigh disease.

  Pincus JH, Solitare GB, Cooper JR. Pincus JH, et al. Arch Neurol. 1976 Nov;33(11):759-63. doi: 10.1001/archneur.1976.00500110027005. Arch Neurol. 1976. PMID: 985153
• Characteristic changes on brain CT in a case of Leigh encephalopathy with deficiency of pyruvate dehydrogenase.

  Arai Y, Miyasato Y, Koide H. Arai Y, et al. Brain Dev. 1991 Nov;13(6):457-8. doi: 10.1016/s0387-7604(12)80050-7. Brain Dev. 1991. PMID: 1810165
• 123I-IMP SPECT findings in mitochondrial encephalomyopathies.

  Fujii T, Okuno T, Ito M, Hattori H, Mutoh K, Go T, Shirasaka Y, Shiraishi H, Iwasaki Y, Asato R. Fujii T, et al. Brain Dev. 1995 Mar-Apr;17(2):89-94. doi: 10.1016/0387-7604(94)00115-e. Brain Dev. 1995. PMID: 7625555
• Phenotypic patterns of MELAS/LS overlap syndrome associated with m.13513G>A mutation, and neuropathological findings in one autopsy case.

  Wang Z, Qi XK, Yao S, Chen B, Luan X, Zhang W, Han M, Yuan Y. Wang Z, et al. Neuropathology. 2010 Dec;30(6):606-14. doi: 10.1111/j.1440-1789.2010.01115.x. Neuropathology. 2010. PMID: 20408961
• Late-adult onset Leigh syndrome.

  McKelvie P, Infeld B, Marotta R, Chin J, Thorburn D, Collins S. McKelvie P, et al. J Clin Neurosci. 2012 Feb;19(2):195-202. doi: 10.1016/j.jocn.2011.09.009. J Clin Neurosci. 2012. PMID: 22273117 Review.
• Rostral brain lesions of Leigh syndrome associated with the mitochondrial DNA 8993T>G mutation.

  Iida Y, Fujii K, Mizuochi H, Suwabe S, Wakui A, Uchikawa H, Shimojo N. Iida Y, et al. J Neurol Sci. 2016 Apr 15;363:77-9. doi: 10.1016/j.jns.2016.02.036. Epub 2016 Feb 16. J Neurol Sci. 2016. PMID: 27000225 No abstract available.