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  • Noncoding RNAs in Duchenne ... Noncoding RNAs in Duchenne and Becker muscular dystrophies: role in pathogenesis and future prognostic and therapeutic perspectives
    Brusa, Roberta; Magri, Francesca; Bresolin, Nereo ... Cellular and molecular life sciences, 11/2020, Volume: 77, Issue: 21
    Journal Article
    Peer reviewed
    Open access

    Noncoding RNAs (ncRNAs), such as miRNAs and long noncoding RNAs, are key regulators of gene expression at the post-transcriptional level and represent promising therapeutic targets and biomarkers for ...
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  • Therapeutic Development in ... Therapeutic Development in Amyotrophic Lateral Sclerosis
    Bucchia, Monica, MS; Ramirez, Agnese, MS; Parente, Valeria, PhD ... Clinical therapeutics, 03/2015, Volume: 37, Issue: 3
    Journal Article
    Peer reviewed

    Abstract Purpose Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease in adults. It is almost invariably lethal within a few years after the onset of symptoms. No effective ...
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  • SOD1 misplacing and mitocho... SOD1 misplacing and mitochondrial dysfunction in amyotrophic lateral sclerosis pathogenesis
    Tafuri, Francesco; Ronchi, Dario; Magri, Francesca ... Frontiers in cellular neuroscience, 08/2015, Volume: 9
    Journal Article
    Peer reviewed
    Open access

    Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease presenting as sporadic (sALS) or familial (fALS) forms. Even if the list of the genes underlining ALS greatly expanded, defects in ...
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  • Recurrence of alopecia area... Recurrence of alopecia areata after covid‐19 vaccination: A report of three cases in Italy
    Rossi, Alfredo; Magri, Francesca; Michelini, Simone ... Journal of cosmetic dermatology, December 2021, Volume: 20, Issue: 12
    Journal Article
    Peer reviewed
    Open access

    Background Common COVID‐19 vaccines side effects are pain at the injection site, muscle pain, fever, headaches, fatigue. Possible immune‐related side effects in predisposed individuals have not been ...
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  • Long-term natural history d... Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53
    Brogna, Claudia; Coratti, Giorgia; Pane, Marika ... PloS one, 06/2019, Volume: 14, Issue: 6
    Journal Article
    Peer reviewed
    Open access

    The aim of this international collaborative effort was to report 36-month longitudinal changes using the 6MWT in ambulant patients affected by Duchenne muscular dystrophy amenable to skip exons 44, ...
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  • The Profiling of 179 miRNA ... The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls
    Magri, Francesca; Napoli, Laura; Ripolone, Michela ... International journal of molecular sciences, 2023-Dec-12, Volume: 24, Issue: 24
    Journal Article
    Peer reviewed
    Open access

    Limb girdle muscular dystrophies (LGMDs) are a group of genetically inherited neuromuscular diseases with a very variable clinical presentation and overlapping traits. Over the last few years there ...
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  • Nusinersen treatment and ce... Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients
    Faravelli, Irene; Meneri, Megi; Saccomanno, Domenica ... Journal of Cellular and Molecular Medicine, March 2020, Volume: 24, Issue: 5
    Journal Article
    Peer reviewed
    Open access

    The antisense oligonucleotide Nusinersen has been recently licensed to treat spinal muscular atrophy (SMA). Since SMA type 3 is characterized by variable phenotype and milder progression, biomarkers ...
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  • Human induced pluripotent s... Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies
    Piga, Daniela; Salani, Sabrina; Magri, Francesca ... Therapeutic Advances in Neurological Disorders, 2019, Volume: 12
    Book Review, Journal Article
    Peer reviewed
    Open access

    Duchenne and Becker muscular dystrophies are the most common muscle diseases and are both currently incurable. They are caused by mutations in the dystrophin gene, which lead to the absence or ...
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  • Ongoing therapeutic trials ... Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy
    Govoni, Alessandra; Magri, Francesca; Brajkovic, Simona ... Cellular and molecular life sciences : CMLS, 12/2013, Volume: 70, Issue: 23
    Journal Article
    Peer reviewed

    Muscular dystrophy is a heterogeneous group of genetic disorders characterised by progressive muscle tissue degeneration. No effective treatment has been discovered for these diseases. Preclinical ...
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