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    Chapter

    Apoptosis and Oxidative Stress in Mitochondrial Disorders

    Mitochondrial encephalomyopathies are clinically heterogeneous disorders under the genetic control of mitochondrial or nuclear DNAs. Since 1988 many qualitative (about one hundred point mutations of tRNA or st...

    S. Servidei, S. Di Giovanni, A. Broccolini, A. D’amico… in Mitochondrial Disorders (2002)

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    Article

    Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findings

    We describe clinical, morphological and biochemical findings of a patient with reducing body myopathy (RBM). This 15-year-old patient was affected by severe limb-girdle progressive myopathy with asymmetric dis...

    E. Bertini, G. Salviati, F. Apollo, E. Ricci, S. Servidei… in Acta Neuropathologica (1994)