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You searched for: Author/Creator Ruggiero, Lucia

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1. An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemia. Issue 1 (8th November 2021)

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)

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

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

5. Multimodal evaluation of an Italian family with a hereditary spastic paraplegia and POLR3A mutations. Issue 11 (21st October 2020)

6. Muscle fiber type disproportion (FTD) in a family with mutations in the LMNA gene. Issue 4 (24th February 2015)

9. Personality traits associated with blepharospasm: A comparison with healthy subjects, patients with facial hemispasm and patients with hyperhidrosis. (April 2020)

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