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kw.\*:("Cytopathie mitochondriale")

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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

DEFICIT ISOLE EN COMPLEXE IV DE LA CHAINE RESPIRATOIRE A PROPOS D'UN CAS = DEFICIENCY IN COMPLEX IV OF MITOCHONDRIAL RESPIRATORY CHAINTEJ, A; SOUA, H; TEBIB, N et al.Revue maghrébine de pédiatrie. 2009, Vol 19, Num 5, pp 253-257, issn 0330-7611, 5 p.Article

Grossesse chez une patiente atteinte de cytopathie mitochondriale = Pregnancy in a patient with mitochondrial diseaseRACINE, A.-C; MANCHOT, G; LE VAILLANT, C et al.Journal de gynécologie obstétrique et biologie de la reproduction. 2004, Vol 33, Num 2, pp 131-139, issn 0368-2315, 9 p.Article

Variabilité clinique et conduite diagnostique des cytopathies mitochondriales : à propos d'une série de 18 cas pédiatriques = Clinical variability and diagnosis steps in childhood mitochondrial diseaseMERCIER, S; JOSSELIN DE WASCH, M; CASTELNAU, P et al.Archives de pédiatrie (Paris). 2009, Vol 16, Num 4, pp 322-330, issn 0929-693X, 9 p.Article

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

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

Le syndrome de Pearson: à propos de 2 observations à révélation néonatale = Neonatal Pearson syndrome. Two case studiesCOLLIN-DUCASSE, H; MAILLOTTE, A.-M; MONPOUX, F et al.Archives de pédiatrie (Paris). 2010, Vol 17, Num 1, pp 38-41, issn 0929-693X, 4 p.Article

Diabète et cardiopathie hypokinétique, quand évoquer une cytopathie mitochondriale ? = Diabetes and hypokinetic cardiopathy: When to consider mitochondrial disease?NOZIERES, C; QUILLASI, V; MOULY-BERTIN, C et al.Annales de cardiologie et d'angéiologie (Paris). 2011, Vol 60, Num 3, pp 176-178, issn 0003-3928, 3 p.Article

Antenatal manifestations of mitochondrial disordersTAVARES, Mariana Vide; SANTOS, Maria João; DOMINGUES, Ana Patricia et al.Journal of inherited metabolic disease. 2013, Vol 36, Num 5, pp 805-811, issn 0141-8955, 7 p.Article

Stratégie diagnostique des maladies mitochondriales = Diagnostic strategy for mitochondrial diseasesCHAUSSENOT, A; PAQUIS-FLUCKLINGER, V.La Lettre du neurologue. 2012, Vol 16, Num 2, pp 45-50, issn 1276-9339, 6 p.Article

A history of mitochondrial diseases : MITOCHONDRIAL MEDICINEDIMAURO, Salvatore.Journal of inherited metabolic disease. 2011, Vol 34, Num 2, pp 261-276, issn 0141-8955, 16 p.Article

PGC-1a/b induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disordersSRIVASTAVA, Sarika; DIAZ, Francisca; IOMMARINI, Luisa et al.Human molecular genetics (Print). 2009, Vol 18, Num 10, pp 1805-1812, issn 0964-6906, 8 p.Article

Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutationSAADA, A; SHAAG, A; ARNON, S et al.Journal of medical genetics. 2007, Vol 44, Num 12, pp 784-786, issn 0022-2593, 3 p.Article

Disorders of mitochondrial protein synthesisJACOBS, Howard T.Human molecular genetics (Print). 2003, Vol 12, pp R293-R301, issn 0964-6906, NS2Article

Modulating heteroplasmyCHINNERY, Patrick F.Trends in genetics (Regular ed.). 2002, Vol 18, Num 4, pp 173-176, issn 0168-9525Article

Liver transplantation for mitochondrial respiratory chain disorders : To be or not to be?DHAWAN, Anil; MIELI-VERGANI, Giorgina.Transplantation. 2001, Vol 71, Num 5, pp 596-598, issn 0041-1337Article

Mitochondrial diseases in man and mouse : MitochondriaWALLACE, D. C.Science (Washington, D.C.). 1999, Vol 283, Num 5407, pp 1482-1488, issn 0036-8075Article

Existe-t-il des rétinopathies d'origine mitochondriale sans atteinte musculaire associée ? = Mitochondrial retinopathy without muscular diseaseDE LA MARNIERRE, E; PARRAU, C; SWALDUZ, B et al.Bulletin des sociétés d'ophtalmologie de France. 1999, Vol 99, pp 29-36, issn 0081-1270Conference Paper

Deficiency of the voltage-dependent anion channel : A novel cause of mitochondriopathyHUIZING, M; RUITTENBEEK, W; THINNES, F. P et al.Pediatric research. 1996, Vol 39, Num 5, pp 760-765, issn 0031-3998Article

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

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