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You searched for: Author/Creator Sframeli, Maria

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1. An observational study of functional abilities in infants, children, and adults with type 1 SMA. (21st August 2018)

2. Burden, professional support, and social network in families of children and young adults with muscular dystrophies. Issue 1 (22nd April 2015)

3. Clinical Variability in Spinal Muscular Atrophy Type III. Issue 6 (2nd October 2020)

4. Different trajectories in upper limb and gross motor function in spinal muscular atrophy. Issue 5 (9th August 2021)

5. Mobility shift of beta-dystroglycan as a marker of GMPPB gene-related muscular dystrophy. Issue 7 (3rd February 2018)

6. Modulation of neuronal nitric oxide synthase and apoptosis by the isoflavone genistein in Mdx mice. (31st August 2015)

7. Molecular analysis of SMARD1 patient-derived cells demonstrates that nonsense-mediated mRNA decay is impaired. Issue 8 (27th January 2022)

8. Nusinersen efficacy data for 24‐month in type 2 and 3 spinal muscular atrophy. Issue 3 (15th February 2022)

9. Nusinersen in pediatric and adult patients with type III spinal muscular atrophy. Issue 8 (24th June 2021)

10. Nusinersen in type 1 spinal muscular atrophy: Twelve‐month real‐world data. Issue 3 (8th July 2019)