Search Results - Spinazzi, Marco

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  1. 1
    Editorial: Application of Omics Approaches to the Diagnosis of Genetic Neurological Disorders

    Editorial: Application of Omics Approaches to the Diagnosis of Genetic Neurological Disorders by Legati, Andrea, Giacopuzzi, Edoardo, Spinazzi, Marco, Lek, Monkol

    Published 2021
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  2. 2
    Generalized Lysosome-Associated Membrane Protein-2 Defect Explains Multisystem Clinical Involvement and Allows Leukocyte Diagnostic Screening in Danon Disease

    Generalized Lysosome-Associated Membrane Protein-2 Defect Explains Multisystem Clinical Involvement and Allows Leukocyte Diagnostic Screening in Danon Disease by Fanin, Marina, Nascimbeni, Anna C., Fulizio, Luigi, Spinazzi, Marco, Melacini, Paola, Angelini, Corrado

    Published 2006
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  3. 3
    Comparison of Corticosteroid Tapering Regimens in Myasthenia Gravis: A Randomized Clinical Trial

    Comparison of Corticosteroid Tapering Regimens in Myasthenia Gravis: A Randomized Clinical Trial by Sharshar, Tarek, Porcher, Raphaël, Demeret, Sophie, Tranchant, Christine, Gueguen, Antoine, Eymard, Bruno, Nadaj-Pakleza, Aleksandra, Spinazzi, Marco, Grimaldi, Lamiae, Birnbaum, Simone, Friedman, Diane, Clair, Bernard

    Published 2021
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  4. 4
    Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients

    Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients by Borgia, Doriana, Malena, Adriana, Spinazzi, Marco, Desbats, Maria Andrea, Salviati, Leonardo, Russell, Aaron P., Miotto, Giovanni, Tosatto, Laura, Pegoraro, Elena, Sorarù, Gianni, Pennuto, Maria, Vergani, Lodovica

    Published 2017
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  5. 5
    PARL deficiency in mouse causes Complex III defects, coenzyme Q depletion, and Leigh-like syndrome

    PARL deficiency in mouse causes Complex III defects, coenzyme Q depletion, and Leigh-like syndrome by Spinazzi, Marco, Radaelli, Enrico, Horré, Katrien, Arranz, Amaia M., Gounko, Natalia V., Agostinis, Patrizia, Maia, Teresa Mendes, Impens, Francis, Morais, Vanessa Alexandra, Lopez-Lluch, Guillermo, Serneels, Lutgarde, Navas, Placido, De Strooper, Bart

    Published 2019
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  6. 6
    Primary coenzyme Q(10) deficiency presenting as fatal neonatal multiorgan failure

    Primary coenzyme Q(10) deficiency presenting as fatal neonatal multiorgan failure by Desbats, Maria Andrea, Vetro, Annalisa, Limongelli, Ivan, Lunardi, Giada, Casarin, Alberto, Doimo, Mara, Spinazzi, Marco, Angelini, Corrado, Cenacchi, Giovanna, Burlina, Alberto, Rodriguez Hernandez, Maria Angeles, Chiandetti, Lino, Clementi, Maurizio, Trevisson, Eva, Navas, Placido, Zuffardi, Orsetta, Salviati, Leonardo

    Published 2015
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