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You searched for: Author/Creator Ricci, Enzo

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1. Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2. Issue 5 (1st February 2016)

2. Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubes. Issue 4 (June 2014)

3. Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1. Issue 12 (17th October 2014)

4. High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients. Issue 10 (8th September 2021)

6. Magnetic resonance imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: Pattern refinement and implications for clinical trials. Issue 5 (4th April 2016)

8. MRI in sarcoglycanopathies: a large international cohort study. Issue 1 (9th September 2017)

9. Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials. (6th December 2021)

10. Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy. Issue 5 (8th December 2018)