All Stories

  1. Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy

    Article • Journal of Cellular and Molecular Medicine, February 2018, Wiley

    Prof. Luisa POLITANO

  2. Galactose-1-phosphate uridyltransferase deficiency: A literature review of the putative mechanisms of short and long-term complications and allelic variants

    Article • Clinical Genetics, August 2017, Wiley

    Prof. Luisa POLITANO

  3. Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy

    Article • The Journal of Gene Medicine, April 2017, Wiley

    Prof. Luisa POLITANO

  4. Emerging perspectives on laminopathies

    Article • Cell Health and Cytoskeleton, April 2016, Dove Medical Press

    Prof. Luisa POLITANO