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You searched for: Author/Creator Rodolico, Carmelo

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1. Aging‐associated genes and let‐7 microRNAs: a contribution to myogenic program dysregulation in oculopharyngeal muscular dystrophy. Issue 6 (12th March 2019)

2. Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1–3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry. Issue 1 (5th January 2016)

4. Efficacy and Safety of Bimagrumab in Sporadic Inclusion Body Myositis: Long-term Extension of RESILIENT. (23rd March 2021)

5. Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes. (1st January 2018)

6. Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes. (31st December 2018)

7. Five years experience on 3, 4-diaminopyridine phosphate in Lambert–Eaton syndrome: Case reports. Issue 38 (September 2017)

8. Genotype–phenotype correlations in valosin-containing protein disease: a retrospective muticentre study. Issue 10 (27th July 2022)

9. Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD). Issue 3 (1st February 2016)

10. Methotrexate as a Steroid-Sparing Agent in Myasthenia Gravis: A Preliminary Retrospective Study. Issue 2 (December 2021)