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Manifestations of the mitochondrial A3243G mutationFINSTERER, Josef.International journal of cardiology. 2009, Vol 137, Num 1, pp 60-62, issn 0167-5273, 3 p.Article

A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsySCIACCO, Monica; PRELLE, Alessandro; BRESOLIN, Nereo et al.Journal of the neurological sciences. 2005, Vol 239, Num 1, pp 21-24, issn 0022-510X, 4 p.Article

Mitochondrial respiratory chain defects : Underlying etiology in various epileptic conditionsYOUNG MOCK LEE; HOON CHUL KANG; JOON SOO LEE et al.Epilepsia (Copenhagen). 2008, Vol 49, Num 4, pp 685-690, issn 0013-9580, 6 p.Article

Mitochondrial dynamics in diseaseCHAN, David C.The New England journal of medicine. 2007, Vol 356, Num 17, pp 1707-1709, issn 0028-4793, 3 p.Article

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Les maladies mitochondriales, un concept émergent? = Mitochondrial diseases a new concept?DESNUELLE, C.La Presse médicale (1983). 2003, Vol 32, Num 27, pp 1251-1252, issn 0755-4982, 2 p.Article

Mitochondrial diseasesDAHL, Hans-Henrick M; THORBURN, David R.American journal of medical genetics. 2001, Vol 106, Num 1, issn 0148-7299, 116 p.Serial Issue

The Psychiatric Manifestations of Mitochondrial Disorders: A Case and Review of the LiteratureANGLIN, Rebecca E; GARSIDE, Sarah L; TARNOPOLSKY, MarkA et al.The Journal of clinical psychiatry. 2012, Vol 73, Num 4, pp 506-512, issn 0160-6689, 7 p.Article

New frontiers in mitochondrial biogenesis and diseaseVillarroya, Francesc.2005, isbn 81-7736-264-X, 1Vol, 220 p., isbn 81-7736-264-XBook

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Identification of a novel compound heterozygote SCO2 mutation in cytochrome c oxidase deficient fatal infantile cardioencephalomyopathyKNUF, M; FABER, J; HUTH, R. G et al.Acta paediatrica (Oslo). 2007, Vol 96, Num 1, pp 130-132, issn 0803-5253, 3 p.Article

MOLECULAR GENETICS OF MITOCHONDRIAL DISORDERSWONG, Lee-Jun C.Developmental disabilities research reviews. 2010, Vol 16, Num 2, pp 154-162, issn 1940-5510, 9 p.Article

Histiocytoid Cardiomyopathy : A Mitochondrial DisorderFINSTERER, Josef.Clinical cardiology (Mahwah, NJ). 2008, Vol 31, Num 5, pp 225-227, issn 0160-9289, 3 p.Article

MERRF-Like Phenotype Associated with a Rare Mitochondrial tRNA^Ile Mutation (m.4284 G>A)HAHN, A; SCHÄNZER, A; NEUBAUER, B. A et al.Neuropediatrics. 2011, Vol 42, Num 4, pp 148-151, issn 0174-304X, 4 p.Article

Mitochondrial Complex I Encephalomyopathy and Cerebral 5-Methyltetrahydrofolate DeficiencyRAMAEKERS, V. T; WELS, J; SEQUEIRA, J. M et al.Neuropediatrics. 2007, Vol 38, Num 4, pp 184-187, issn 0174-304X, 4 p.Article

Transduction of Human Recombinant Proteins into Mitochondria as a Protein Therapeutic Approach for Mitochondrial DisordersPAPADOPOULOU, Lefkothea C; TSIFTSOGLOU, Asterios S.Pharmaceutical research. 2011, Vol 28, Num 11, pp 2639-2656, issn 0724-8741, 18 p.Article

Multisystem manifestations of mitochondrial disordersDI DONATO, Stefano.Journal of neurology. 2009, Vol 256, Num 5, pp 693-710, issn 0340-5354, 18 p.Article

Disorders from perturbations of nuclear-mitochondrial intergenomic cross-talkSPINAZZOLA, A; ZEVIANI, M.Journal of internal medicine. 2009, Vol 265, Num 2, pp 174-192, issn 0954-6820, 19 p.Conference Paper

A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathySANTORO, L; MANGANELLI, F; LANZILLO, R et al.Journal of neurology. 2006, Vol 253, Num 7, pp 869-874, issn 0340-5354, 6 p.Article

MPVI7 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsGARONE, Caterina; RUBIO, Juan Carlos; CALVO, Sarah E et al.Archives of neurology (Chicago). 2012, Vol 69, Num 12, pp 1648-1651, issn 0003-9942, 4 p.Article

Ophthalmological findings in children and young adults with genetically verified mitochondrial diseaseGRÖNLUND, M. A; SEYEDI HONARVAR, A. K; ANDERSSON, S et al.British journal of ophthalmology. 2010, Vol 94, Num 1, pp 121-127, issn 0007-1161, 7 p.Article

Mitochondrial DNA Mutations in Disease and AgingWALLACE, Douglas C.Environmental and molecular mutagenesis (Print). 2010, Vol 51, Num 5, pp 440-450, issn 0893-6692, 11 p.Article

Mitochondrial Dysfunction in AutismGIULIVI, Cecilia; ZHANG, Yi-Fan; OMANSKA-KLUSEK, Alicja et al.JAMA, the journal of the American Medical Association. 2010, Vol 304, Num 21, pp 2389-2396, issn 0098-7484, 8 p.Article

Central Nervous System Imaging in Mitochondrial DisordersFINSTERER, Josef.Canadian journal of neurological sciences. 2009, Vol 36, Num 2, pp 143-153, issn 0317-1671, 11 p.Article