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Les myopathies mitochondriales = Mitochondrial myopathiesEYMARD, B.La Revue du praticien (Paris). 1988, Num 22, pp 1522-1528, issn 0035-2640Article

Histopathological observation of the heart with diffuse and abnormal proliferation of mitochondria in myocardial cells (mitochondrial cardiomyopathy): report of an adult caseKAJIHARA, H; ODA, N; TAHARA, E et al.Heart and vessels. 1986, Vol 2, Num 4, pp 233-238, issn 0910-8327Article

Ubidecarenone in the treatment of mitochondrial myopathies : a multi-center double-blind trialBRESOLIN, N; DORIGUZZI, C; PICCOLO, G et al.Journal of the neurological sciences. 1990, Vol 100, Num 1-2, pp 70-78, issn 0022-510XArticle

Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)SEIBEL, P; DEGOUL, F; KADENBACH, B et al.Journal of the neurological sciences. 1991, Vol 105, Num 2, pp 217-224, issn 0022-510XArticle

Carnitine palmitoyl transferase deficiency with an atypical presentation and ultrastructural mitochondrial abnormalitiesCAREY, M. P; POULTON, K; HAWKINS, C et al.Journal of neurology, neurosurgery and psychiatry. 1987, Vol 50, Num 8, pp 1060-1062, issn 0022-3050Article

Le dysfonctionnement mitochondrial en pathologie humaine = Mitochondrial dysfonction in human pathologyGENY, C; AMSELEM, S; DANAN, C et al.Annales de médecine interne (Paris). 1992, Vol 143, Num 2, pp 128-135, issn 0003-410XArticle

Les encéphalomyopathies mitochondriales = Mitochondrial encephalomyopathiesGENY, C; CESARO, P; AMSELEM, S et al.La Semaine des hôpitaux de Paris. 1991, Vol 67, Num 1-2, pp 30-34, issn 0037-1777Article

Mitochondrial myopathy with a defect of mitochondrial-protein transportSCHAPIRA, A. H. V; COOPER, J. M; MORGAN-HUGHES, J. A et al.The New England journal of medicine. 1990, Vol 323, Num 1, pp 37-42, issn 0028-4793Article

Cytoplasmic body and mitochondrial DNA deletionSAHASHI, K; OHNO, K; TANAKA, M et al.Journal of the neurological sciences. 1990, Vol 99, Num 2-3, pp 291-300, issn 0022-510XArticle

The syndrome of myoclonic epilepsy with ragged-red fibers. Report of a case and review of the literatureGARCIA SILVA, M. T; AICARDI, J; GOUTIERES, F et al.Neuropediatrics. 1987, Vol 18, Num 4, pp 200-204, issn 0174-304XArticle

Anesthetic management of two patients with mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS)ITAYA, K; TAKAHATA, O; MAMIYA, K et al.Masui. 1995, Vol 44, Num 5, pp 710-712, issn 0021-4892Article

A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathiesHAMMANS, S. R; SWEENEY, M. G; WICKS, D. A. G et al.Brain. 1992, Vol 115, pp 343-365, issn 0006-8950, 2Article

Treatment of experimental NADH ubiquinone reductase deficiency with menadioneCOOPER, J. M; HAYES, D. J; CHALLISS, R. A. J et al.Brain. 1992, Vol 115, pp 991-1000, issn 0006-8950, 4Article

Biopsies musculaire et cérébrale d'un cas d'encéphalomyopathie mitochondriale : mise en évidence d'une vasculopathie mitochondriale = Muscle and brain biopsies in one case of mitochondrial encephalomyopathy: demonstration of mitochondrial vascular diseaseCOQUET, M; FONTAN, D; VITAL, C et al.Annales de pathologie (Paris). 1990, Vol 10, Num 3, pp 181-186, issn 0242-6498Article

Peripheral neuropathy in mitochondrial diseasePEZESHKPOUR, G; KRARUP, C; BUCHTHAL, F et al.Journal of the neurological sciences. 1987, Vol 77, Num 2-3, pp 285-304, issn 0022-510XArticle

Mitochondrial diseaseAnnals of the New York Academy of Sciences. 1986, Vol 488, pp 1-153, issn 0077-8923Conference Proceedings

Die klinische Symptomatik von Netzhautdystrophien bei Mitochondriopathien = La symptomatologie clinique des dystrophies rétiniennes dans les mitochondropathies = Variety of retinal changes in mitochondriopathiesHAMMERSTEIN, W; BOSCHE, J.Fortschritte der Ophthalmologie. 1988, Vol 85, Num 5, pp 505-507, issn 0723-8045Conference Paper

Defective brain energy metabolism shown by in vivo ³¹P MR spectroscopy in 28 patients with mitochondrial cytopathiesBARBIROLI, B; MONTAGNA, P; MARTINELLI, P et al.Journal of cerebral blood flow and metabolism. 1993, Vol 13, Num 3, pp 469-474, issn 0271-678XArticle

Mitochondrial DNA expression in mitochondrial myopathies and coordinated expression of nuclear genes involved in ATP productionHEDDI, A; LESTIENNE, P; WALLACE, D. C et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 16, pp 12156-12163, issn 0021-9258Article

The use of chorionic villi in prenatal diagnosis of mitochondriopathiesRUITENBEEK, W; SENGERS, R. C. A; TRIJBELS, J. M. F et al.Journal of inherited metabolic disease. 1992, Vol 15, Num 3, pp 303-306, issn 0141-8955Conference Paper

Spätmanifestation einer mitochondrialen Myopathie : Komplex-I- und -IV-Mangel der mitochondrialen Atmungskette mit progredienten ParesenBEYENBURG, S; VON WERSEBE, O; ZIERZ, S et al.Nervenarzt. 1991, Vol 62, Num 8, pp 506-511, issn 0028-2804Article

EEG findings in children and adolescents with mitochondrial encephalomyopathies : a study of 25 casesTULINIUS, M. H; HAGNE, I.Brain & development (Tokyo. 1979). 1991, Vol 13, Num 3, pp 167-173, issn 0387-7604Article

Myopathie à mitochondries et signes oculairesBRON, A; GIROUD, M; BORSOTTI, P et al.Bulletin des sociétés d'ophtalmologie de France. 1991, Vol 91, Num 5, pp 521-523, issn 0081-1270Article

Mutations of the mitochondrial DNA : the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathiesGERBITZ, K.-D; OBERMAIER-KUSSER, B; LESTIENNE, P et al.Journal of clinical chemistry and clinical biochemistry. 1990, Vol 28, Num 4, pp 241-250, issn 0340-076XArticle