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You searched for: Author/Creator Garibaldi, Matteo

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1. Combined proteomic and lipidomic studies in Pompe disease allow a better disease mechanism understanding. Issue 3 (28th December 2020)

2. Expanding the spectrum of genes responsible for hereditary motor neuropathies. Issue 10 (5th June 2019)

3. Gender effect on cardiac involvement in myotonic dystrophy type 1. (25th December 2020)

4. Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndrome. Issue 8 (28th July 2018)

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

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

9. Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide Survey. (14th March 2023)

10. Recessive MYPN mutations cause cap myopathy with occasional nemaline rods. Issue 3 (20th March 2017)