Resultats de la cerca - Massimo Zeviani

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  1. 1
    Mitochondrial disorders

    Mitochondrial disorders per Massimo Zeviani

    Publicat 2004
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  2. 2
    Disorders from perturbations of nuclear‐mitochondrial intergenomic cross‐talk

    Disorders from perturbations of nuclear‐mitochondrial intergenomic cross‐talk per Antonella Spinazzola, Massimo Zeviani

    Publicat 2009
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  3. 3
    Altered Sulfide (H2S) Metabolism in Ethylmalonic Encephalopathy

    Altered Sulfide (H2S) Metabolism in Ethylmalonic Encephalopathy per Valeria Tiranti, Massimo Zeviani

    Publicat 2013
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  4. 4
    MtDNA‐maintenance defects: syndromes and genes

    MtDNA‐maintenance defects: syndromes and genes per Carlo Viscomi, Massimo Zeviani

    Publicat 2017
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  5. 5
    Human diseases associated with defects in assembly of OXPHOS complexes

    Human diseases associated with defects in assembly of OXPHOS complexes per Daniele Ghezzi, Massimo Zeviani

    Publicat 2018
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  6. 6
    Strategies for fighting mitochondrial diseases

    Strategies for fighting mitochondrial diseases per Carlo Viscomi, Massimo Zeviani

    Publicat 2020
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  7. 7
    Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions

    Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions per Margherita Protasoni, Massimo Zeviani

    Publicat 2021
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  8. 8
    Mitochondrial Retinopathies

    Mitochondrial Retinopathies per Massimo Zeviani, Valério Carelli

    Publicat 2021
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  9. 9
    Mitochondrial Neurodegeneration

    Mitochondrial Neurodegeneration per Massimo Zeviani, Carlo Viscomi

    Publicat 2022
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  10. 10
    Nuclear gene mutations as the cause of mitochondrial complex III deficiency

    Nuclear gene mutations as the cause of mitochondrial complex III deficiency per Erika Fernández‐Vizarra, Massimo Zeviani

    Publicat 2015
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  11. 11
    Mitochondrial complex III Rieske Fe-S protein processing and assembly

    Mitochondrial complex III Rieske Fe-S protein processing and assembly per Erika Fernández‐Vizarra, Massimo Zeviani

    Publicat 2017
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  12. 12
    Mitochondrial disorders of the OXPHOS system

    Mitochondrial disorders of the OXPHOS system per Erika Fernández‐Vizarra, Massimo Zeviani

    Publicat 2020
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  13. 13
    Emerging concepts in the therapy of mitochondrial disease

    Emerging concepts in the therapy of mitochondrial disease per Carlo Viscomi, Emanuela Bottani, Massimo Zeviani

    Publicat 2015
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  14. 14
    Myofibrillar-protein isoforms and sarcoplasmic-reticulum Ca2+-transport activity of single human muscle fibres

    Myofibrillar-protein isoforms and sarcoplasmic-reticulum Ca2+-transport activity of single human muscle fibres per G. Salviati, Romeo Betto, Daniela Danieli‐Betto, Massimo Zeviani

    Publicat 1984
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  15. 15
    Mitochondrial medicine: A metabolic perspective on the pathology of oxidative phosphorylation disorders

    Mitochondrial medicine: A metabolic perspective on the pathology of oxidative phosphorylation disorders per Jan Smeitink, Massimo Zeviani, Douglass M. Turnbull, Howard T. Jacobs

    Publicat 2006
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  16. 16
    Complex I deficiency is Associated with 3243G:C Mitochondrial DNA in Osteosarcoma Cell Cybrids

    Complex I deficiency is Associated with 3243G:C Mitochondrial DNA in Osteosarcoma Cell Cybrids per Donald R. Dunbar, Pamela Moonie, Massimo Zeviani, Ian Holt

    Publicat 1996
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  17. 17
    Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA)

    Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA) per Erika Fernández‐Vizarra, Angela Berardinelli, Lucia Valente, Valeria Tiranti, Massimo Zeviani

    Publicat 2006
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  18. 18
    Expression of the SMN Gene, the Spinal Muscular Atrophy Determining Gene, in the Mammalian Central Nervous System

    Expression of the SMN Gene, the Spinal Muscular Atrophy Determining Gene, in the Mammalian Central Nervous System per Giorgio Battaglia, Alessandra P. Princivalle, Francesca Forti, Carlotta Lizier, Massimo Zeviani

    Publicat 1997
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  19. 19
    AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome

    AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome per Ivano Di Meo, Silvia Marchet, Costanza Lamperti, Massimo Zeviani, Carlo Viscomi

    Publicat 2017
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  20. 20
    Loss of apoptosis-inducing factor critically affects MIA40 function

    Loss of apoptosis-inducing factor critically affects MIA40 function per Katharina Meyer, Sabrina Buettner, Daniele Ghezzi, Massimo Zeviani, Daniele Bano, Pierluigi Nicotera

    Publicat 2015
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