Mitochondrial disorders as windows into an ancient organelleVAFAI, Scott B; MOOTHA, Vamsi K.Nature (London). 2012, Vol 491, Num 7424, pp 374-383, issn 0028-0836, 10 p.Article

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 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

Mitochondrial diseaseSCHAPIRA, Anthony H. V.Lancet (British edition). 2006, Vol 368, Num 9529, pp 70-82, issn 0140-6736, 13 p.Article

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

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

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

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

Preventing transmission of maternally inherited mitochondrial DNA diseasesPOULTON, Joanna; KENNEDY, Stephen; OAKESHOTT, Pippa et al.BMJ. British medical journal (International ed.). 2009, Vol 338, Num 7690, pp 345-349, issn 0959-8146, 5 p.Article

Review of the literature on major mental disorders in adult patients with mitochondrial diseasesFATTAL, Omar; BUDUR, Kumar; VAUGHAN, Aaron J et al.Psychosomatics (Washington, DC). 2006, Vol 47, Num 1, pp 1-7, issn 0033-3182, 7 p.Article

Mitochondrial disorders: A proposal for consensus diagnostic criteria in infants and childrenWOLF, Nicole I; SMEITINK, Jan A. M.Neurology. 2002, Vol 59, Num 9, pp 1402-1405, issn 0028-3878, 4 p.Article

Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke evaluation of mutations by using sequence data on the entire coding regionFINNILÄ, Saara; HASSINEN, Ilmo E; MAJAMAA, Kari et al.Mutation Research. Mutation research genomics (Print). 2001, Vol 458, Num 1-2, pp 31-39, issn 1383-5726Article

Macro-EMG in mitochondriopathyFINSTERER, J; FUGLSANG-FREDERIKSEN, A.Clinical neurophysiology. 1999, Vol 110, Num 8, pp 1466-1470, issn 1388-2457Article