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Journal Abstract Search

359 related items for PubMed ID: 23849057

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  • 3. Cardiomyopathy in Friedreich's ataxia.
    Rahman F, Pandolfo M.
    Acta Neurol Belg; 2011 Sep; 111(3):183-7. PubMed ID: 22141280
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  • 6. Progressive mitochondrial protein lysine acetylation and heart failure in a model of Friedreich's ataxia cardiomyopathy.
    Stram AR, Wagner GR, Fogler BD, Pride PM, Hirschey MD, Payne RM.
    PLoS One; 2017 Sep; 12(5):e0178354. PubMed ID: 28542596
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  • 7. Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich's ataxia.
    Igoillo-Esteve M, Gurgul-Convey E, Hu A, Romagueira Bichara Dos Santos L, Abdulkarim B, Chintawar S, Marselli L, Marchetti P, Jonas JC, Eizirik DL, Pandolfo M, Cnop M.
    Hum Mol Genet; 2015 Apr 15; 24(8):2274-86. PubMed ID: 25552656
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  • 8. Neurodegeneration in Friedreich's ataxia: from defective frataxin to oxidative stress.
    Gomes CM, Santos R.
    Oxid Med Cell Longev; 2013 Apr 15; 2013():487534. PubMed ID: 23936609
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  • 11. Friedreich's ataxia: clinical aspects and pathogenesis.
    Pandolfo M.
    Semin Neurol; 1999 Apr 15; 19(3):311-21. PubMed ID: 12194387
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  • 12. Does oxidative stress contribute to the pathology of Friedreich's ataxia? A radical question.
    Armstrong JS, Khdour O, Hecht SM.
    FASEB J; 2010 Jul 15; 24(7):2152-63. PubMed ID: 20219987
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  • 13. PPAR gamma agonist leriglitazone improves frataxin-loss impairments in cellular and animal models of Friedreich Ataxia.
    Rodríguez-Pascau L, Britti E, Calap-Quintana P, Dong YN, Vergara C, Delaspre F, Medina-Carbonero M, Tamarit J, Pallardó FV, Gonzalez-Cabo P, Ros J, Lynch DR, Martinell M, Pizcueta P.
    Neurobiol Dis; 2021 Jan 15; 148():105162. PubMed ID: 33171227
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  • 14. Deferiprone and idebenone rescue frataxin depletion phenotypes in a Drosophila model of Friedreich's ataxia.
    Soriano S, Llorens JV, Blanco-Sobero L, Gutiérrez L, Calap-Quintana P, Morales MP, Moltó MD, Martínez-Sebastián MJ.
    Gene; 2013 Jun 01; 521(2):274-81. PubMed ID: 23542074
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  • 15. Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.
    Puccio H, Simon D, Cossée M, Criqui-Filipe P, Tiziano F, Melki J, Hindelang C, Matyas R, Rustin P, Koenig M.
    Nat Genet; 2001 Feb 01; 27(2):181-6. PubMed ID: 11175786
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