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Oxidative stress biomarkers in mitochondrial myopathies, basally and after cysteine donor supplementationMANCUSO, Michelangelo; ORSUCCI, Daniele; LOGERFO, Annalisa et al.Journal of neurology. 2010, Vol 257, Num 5, pp 774-781, issn 0340-5354, 8 p.Article

Genetic variants in nuclear-encoded mitochondrial proteins are associated with oxidative stress in obsessive compulsive disordersORHAN, Nurcan; KUCUKALI, Cem Ismail; CAKIR, Ulku et al.Journal of psychiatric research. 2012, Vol 46, Num 2, pp 212-218, issn 0022-3956, 7 p.Article

Heterogeneous patterns of tissue injury in NARP syndromeGELFAND, Jeffrey M; DUNCAN, Jacque L; RACINE, Caroline A et al.Journal of neurology. 2011, Vol 258, Num 3, pp 440-448, issn 0340-5354, 9 p.Article

A new mitochondrial point mutation in the transfer RNALys gene associated with progressive external ophthalmoplegia with impaired respiratory regulationWOLF, Joachim; OBERMAIER-KUSSER, Bert; JACOBS, Martina et al.Journal of the neurological sciences. 2012, Vol 316, Num 1-2, pp 108-111, issn 0022-510X, 4 p.Article

Specific electron transport chain abnormalities in amyotrophic lateral sclerosisLIN, Jerry; DIAMANDUROS, Andrew; CHOWDHURY, Soheli A et al.Journal of neurology. 2009, Vol 256, Num 5, pp 774-782, issn 0340-5354, 9 p.Article

Skeletal muscle ultrasonography in children with a dysfunction in the oxidative phosphorylation systemPILLEN, S; MORAVA, E; VAN KEIMPEMA, M et al.Neuropediatrics. 2006, Vol 37, Num 3, pp 142-147, issn 0174-304X, 6 p.Article

Proton Magnetic Resonance Spectroscopy and MRI Reveal No Evidence for Brain Mitochondrial Dysfunction in Children with Autism Spectrum DisorderCORRIGAN, Neva M; SHAW, Dennis W. W; RICHARDS, Todd L et al.Journal of autism and developmental disorders. 2012, Vol 42, Num 1, pp 105-115, issn 0162-3257, 11 p.Article

Mitochondrial dementia: A sporadic case of progressive cognitive and behavioral decline with hearing loss due to the rare m.3291T>C MELAS mutationSALSANO, Ettore; GIOVAGNOLI, Anna Rita; MORANDI, Lucia et al.Journal of the neurological sciences. 2011, Vol 300, Num 1-2, pp 165-168, issn 0022-510X, 4 p.Article

Successful TAT-mediated enzyme replacement therapy in a mouse model of mitochondrial E3 deficiencyRAPOPORT, Matan; SALMAN, Lina; SABAG, Ofra et al.Journal of molecular medicine (Berlin. Print). 2011, Vol 89, Num 2, pp 161-170, issn 0946-2716, 10 p.Article

Stoffwechselstörungen mit typischen Veränderungen im MRT : MR-Spektroskopie im ZNS = Metabolic disorders with typical alterations in MRI : MR spectroscopy in the CNSWARMUTH-METZ, M.Der Radiologe (Berlin. Print). 2010, Vol 50, Num 9, pp 775-783, issn 0033-832X, 9 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

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

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

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

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

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

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

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

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

Mitochondrial diseasesSCHAPIRA, Anthony H. V.Lancet (British edition). 2012, Vol 379, Num 9828, pp 1825-1834, issn 0140-6736, 10 p.Article

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