Encéphalopathie nécrosante subaiguë, maladie de Leigh: à propos d'un cas = Subacute necrotizing encephalopathy (Leigh's disease). Case reportDELISLE, M. B; NETTER, J. C; PEYRILLE, F et al.Annales de pathologie (Paris). 1985, Vol 5, Num 4-5, pp 313-317, issn 0242-6498Article

Chronic relapsing course of encephalomyeloradiculopathy in a 6-year-old boyRIIKONEN, R; DONNER, M.Neuropediatrics. 1987, Vol 18, Num 4, pp 235-238, issn 0174-304XArticle

Rolandic Mitochondrial Encephalomyelopathy and MT-ND3 MutationsWERNER, Klaus G. E; MOREL, Chantal F; FEIGENBAUM, Annette S. J et al.Pediatric neurology. 2009, Vol 41, Num 1, pp 27-33, issn 0887-8994, 7 p.Article

Congenital encephalomyopathy with epilepsy, chorioretinitis, basal ganglia involvement, and muscle minicoresAVONI, P; MONARI, L; CARELLI, V et al.Annals of neurology. 2000, Vol 47, Num 3, pp 395-399, issn 0364-5134Article

Extremely high levels of mutant mtDNAs co-localize with cytochrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243PETRUZZELLA, V; MORAES, C. T; SANO, M. C et al.Human molecular genetics (Print). 1994, Vol 3, Num 3, pp 449-454, issn 0964-6906Article

Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathiesHESS, J. F; PARISI, M. A; BENNETT, J. L et al.Nature (London). 1991, Vol 351, Num 6323, pp 236-239, issn 0028-0836, 4 p.Article

Mitochondrial abnormalities in choroid plexus of Leigh diseaseOHAMA, E; IKUTA, F; NAKAMURA, N et al.Brain & development (Tokyo. 1979). 1988, Vol 10, Num 1, pp 30-35, issn 0387-7604Article

Activation of endoplasmic reticulum stress signaling pathway is associated with neuronal degeneration in MoMuLV-ts1-induced spongiform encephalomyelopathyKIM, Hun-Taek; WATERS, Kara; STOICA, George et al.Laboratory investigation. 2004, Vol 84, Num 7, pp 816-827, issn 0023-6837, 12 p.Article

Interferon production by mononuclear cells from patients with chronic fatigue syndromeMILTON, J. D; MORRIS, A. G; CHRISTMAS, S. E et al.Medical science research. 1991, Vol 19, Num 7, pp 205-206, issn 0269-8951Article

Ubiquinone: cholesterol's reclusive cousinHARGREAVES, Iain P.Annals of clinical biochemistry. 2003, Vol 40, pp 207-218, issn 0004-5632, 12 p., 3Article

Diagnosis and management of mitochondrial diseasesGILLIS, Lynette; KAYE, Edward.The Pediatric clinics of North America. 2002, Vol 49, Num 1, pp vii-viii, issn 0031-3955, 18 p.Article

Immunohistochemical demonstration of spinal ventral horn cells involvement in a case of myoclonus epilepsy with ragged red fibers (MERRF)SPARACO, M; CAVALLARO, T; ROSSI, G et al.Clinical neuropathology. 2000, Vol 19, Num 4, pp 200-207, issn 0722-5091Article

The therapy of respiratory chain encephalomyopathy : a critical review of the past and current perspectiveWALKER, U. A; BYRNE, E.Acta neurologica scandinavica. 1995, Vol 92, Num 4, pp 273-280, issn 0001-6314Article

Alteration from T- to B-cell tropism reduces thymic atrophy and cytocidal effects in thymocytes but not neurovirulence induced by ts1, a mutant of Moloney murine leukemia virus TBWONG, P. K. Y; SZUREK, P. F; FLOYD, E et al.Proceedings of the National Academy of Sciences of the United States of America. 1991, Vol 88, Num 20, pp 8991-8995, issn 0027-8424Article

Encephalomyelopahtie, Kardiomyopathie, Kataract und Pigmentepithelveränderungen der Retina infolge eines Cytochrom-c-Oxidase-Mangels = Encéphalomyélopathie, cardiomyopathie, cataracte et modifications de l'épithélium pigmentaire rétinien dues à un déficit en cytochrome c oxydase = Encephalomyelopathy, cardiomyopathy, cataract, and changes of the retinal pigment epithelium resulting from cytochrome c oxydase, deficiencySIEVERDING, L; SCHMALTZ, A. A; APITZ, J et al.Klinische Pädiatrie. 1988, Vol 200, Num 5, pp 381-387, issn 0300-8630Article

Anaesthesia for an adolescent with mitochondrial encephalomyopathy-lactic acidosis-stroke-like episodes syndromeBOLTON, P; PEUTRELL, J; ZUBERI, S et al.Paediatric anaesthesia (Paris). 2003, Vol 13, Num 5, pp 453-456, issn 1155-5645, 4 p.Article

Encephalomyeloradiculopathy associated with Epstein-Barr virus : primary infection or reactivation?MERELLI, E; BEDIN, R; SOLA, P et al.Acta neurologica scandinavica. 1997, Vol 96, Num 6, pp 416-420, issn 0001-6314Article

Glutaric acidemia type II : neuroimaging and spectroscopy evidence for developmental encephalomyopathySHEVELL, M. I; DIDOMENICANTONIO, G; SYLVAIN, M et al.Pediatric neurology. 1995, Vol 12, Num 4, pp 350-353, issn 0887-8994Article

Polarographic studies of saponin-skinned muscle fibres in patients with mitochondrial myopathiesSPERL, W; SKLADAL, D; LANZNASTER, N et al.Journal of inherited metabolic disease. 1994, Vol 17, Num 3, pp 307-310, issn 0141-8955Conference Paper

HMPAO-SPECT and MRI in acute disseminated encephalomyelitisBROICH, K; HORWICH, D; ALAVI, A et al.JNM. The journal of nuclear medicine : (1990). 1991, Vol 32, Num 10, pp 1897-1900Article

Epidémiologie biologique et clinique des infections onco-rétrovirales HTLV-I et II. DiscussionDE THE, G; BASTIN, R; PENE, P et al.Bulletin de l'Académie nationale de médecine. 1991, Vol 175, Num 6, pp 861-870, issn 0001-4079Article

Infantile beriberi presenting as subacute necrotizing encephalomyelopathyWYATT, D. T; NOETZEL, M. J; HILLMAN, R. E et al.The Journal of pediatrics. 1987, Vol 110, Num 6, pp 888-892, issn 0022-3476Article

The effect of silyl substituted methotrexate in the treatment of experimental allergic encephalomyelitis in rats mediated by T-line cellsPRZUNTEK, H; WESTARP, M. E; VOHL, M. L et al.Neuropharmacology. 1987, Vol 26, Num 2-3, pp 255-260, issn 0028-3908Article

Up-regulation of pro-nerve growth factor, neurotrophin receptor p75, and sortilin is associated with retrovirus-induced spongiform encephalomyelopathySTOICA, George; LUNGU, Gina; KIM, Hun-Taek et al.Brain research. 2008, Vol 1208, pp 204-216, issn 0006-8993, 13 p.Article

Apoptosis is suspended in muscle of mitochondrial encephalomyopathiesIKEZOE, Koji; NAKAGAWA, Masahiro; YAN, Chuanzhu et al.Acta neuropathologica. 2002, Vol 103, Num 6, pp 531-540, issn 0001-6322Article