Resultados de procura - Massimo Zeviani

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  1. 1
    Mitochondrial disorders

    Mitochondrial disorders por Massimo Zeviani

    Publicado 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 por Antonella Spinazzola, Massimo Zeviani

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

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

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

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

    Publicado 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 por Daniele Ghezzi, Massimo Zeviani

    Publicado 2018
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  6. 6
    Strategies for fighting mitochondrial diseases

    Strategies for fighting mitochondrial diseases por Carlo Viscomi, Massimo Zeviani

    Publicado 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 por Margherita Protasoni, Massimo Zeviani

    Publicado 2021
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  8. 8
    Mitochondrial Retinopathies

    Mitochondrial Retinopathies por Massimo Zeviani, Valério Carelli

    Publicado 2021
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  9. 9
    Mitochondrial Neurodegeneration

    Mitochondrial Neurodegeneration por Massimo Zeviani, Carlo Viscomi

    Publicado 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 por Erika Fernández‐Vizarra, Massimo Zeviani

    Publicado 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 por Erika Fernández‐Vizarra, Massimo Zeviani

    Publicado 2017
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  12. 12
    Mitochondrial disorders of the OXPHOS system

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

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

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

    Publicado 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 por G. Salviati, Romeo Betto, Daniela Danieli‐Betto, Massimo Zeviani

    Publicado 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 por Jan Smeitink, Massimo Zeviani, Douglass M. Turnbull, Howard T. Jacobs

    Publicado 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 por Donald R. Dunbar, Pamela Moonie, Massimo Zeviani, Ian Holt

    Publicado 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) por Erika Fernández‐Vizarra, Angela Berardinelli, Lucia Valente, Valeria Tiranti, Massimo Zeviani

    Publicado 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 por Giorgio Battaglia, Alessandra P. Princivalle, Francesca Forti, Carlotta Lizier, Massimo Zeviani

    Publicado 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 por Ivano Di Meo, Silvia Marchet, Costanza Lamperti, Massimo Zeviani, Carlo Viscomi

    Publicado 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 por Katharina Meyer, Sabrina Buettner, Daniele Ghezzi, Massimo Zeviani, Daniele Bano, Pierluigi Nicotera

    Publicado 2015
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