S. Jabeen, G. Sandeep, K. Mridula, A. Meena, R. Borgohain et al., Adult-onset Leigh???s disease: A rare entity, Annals of Indian Academy of Neurology, vol.19, issue.1, pp.140-142, 2016.
DOI : 10.4103/0972-2327.175437

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782535

N. Huertas-gonzález, V. Hernando-requejo, Z. Luciano-garcía, and J. Cervera-rodilla, Wernicke???s Encephalopathy, Wet Beriberi, and Polyneuropathy in a Patient with Folate and Thiamine Deficiency Related to Gastric Phytobezoar, Case Reports in Neurological Medicine, vol.101, issue.1, article e10, pp.624807-624810, 2015.
DOI : 10.1212/01.wnl.0000099189.56741.a7

S. Busani, C. Bonvecchio, A. Gaspari, M. Malagoli, A. Todeschini et al., Wernicke???s encephalopathy in a malnourished surgical patient: a difficult diagnosis, BMC Research Notes, vol.7, issue.1, p.718, 2014.
DOI : 10.3174/ajnr.A2359

J. Cameron, N. Mackay, A. Feigenbaum, M. Tarnopolsky, S. Blaser et al., Exome sequencing identifies complex I NDUFV2 mutations as a novel cause of Leigh syndrome, European Journal of Paediatric Neurology, vol.19, issue.5, pp.525-557, 2015.
DOI : 10.1016/j.ejpn.2015.05.002

S. Ferdinandusse, H. Waterham, S. Heales, G. Brown, I. Hargreaves et al., HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase, Orphanet Journal of Rare Diseases, vol.8, issue.1, pp.188-194, 2013.
DOI : 10.1086/430843

H. Blondon, M. Polivka, F. Joly, B. Flourie, J. Mikol et al., Digestive smooth muscle mitochondrial myopathy in patients with mitochondrial-neuro-gastro-intestinal encephalomyopathy (MNGIE), Gastroent??rologie Clinique et Biologique, vol.29, issue.8-9, pp.773-781, 2005.
DOI : 10.1016/S0399-8320(05)86346-8

C. Quinzii, S. Dimauro, and M. Hirano, Human Coenzyme Q10 Deficiency, Neurochemical Research, vol.62, issue.4-5, pp.723-730, 2007.
DOI : 10.1002/biof.5520250113

URL : https://link.springer.com/content/pdf/10.1007%2Fs11064-006-9190-z.pdf