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S. Benedetti

Laboratory of Molecular Biology

14

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81

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P3170Innovative approach for risk stratification of LMNA-related cardiomyopathy: results from an integrated cardiological and neurological 10-year follow-up multicentre study

2018 European Heart Journal
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4792Late gadolinium enhancement and arrhythmic risk prediction in patients with LMNA-related cardiomyopathy: results from a long-term follow-up multicenter study

2017 European Heart Journal
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Clinical aspects of cardiolaminopathies and prospects for a cardiolaminopathy registry.

2015 Orphanet Journal of Rare Diseases
- S. Benedetti
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Evaluation of damaging effects of splicing mutations: Validation of a method useful to diagnostic laboratories

2013 Clinical Biochemistry
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Compound heterozygous SCN5A gene mutations in asymptomatic Brugada syndrome child

2012
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Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers.

2012 Biochimica et Biophysica Acta
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O-4The Italian Network for Laminopathies

2011
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P3.1 Brown–Vialetto–Van Laere and Fazio Londe overlap sindromes: A clinical, biochemical and genetic study in 6 patients

2011 Neuromuscular Disorders
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Novel LMNA gene mutation in a patient with cardiac and skeletal muscle involvement

2009 Journal of Neurology
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G.P.4.05 Phenotypic clustering of lamin A/C mutations in neuromuscular patients

2006 Neuromuscular Disorders
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