S. Benedetti

Phenotypic clustering of lamin A/C mutations in neuromuscular patients

E. Bertini, G. Comi, R. Caldara, 2007, Neurology.

Prevalent cardiac phenotype resulting in heart transplantation in a novel LMNA gene duplication

G. Alí, M. Emdin, D. Caramella, 2010, Neuromuscular Disorders.

Two patients with ‘Dropped head syndrome’ due to mutations in LMNA or SEPN1 genes

A. D’Amico, S. Benedetti, E. Bertini, 2005, Neuromuscular Disorders.

Brown–Vialetto–van Laere and Fazio–Londe overlap syndromes: A clinical, biochemical and genetic study

E. Bertini, A. Bizzi, A. D’Amico, 2012, Neuromuscular Disorders.

Laminopathies: many diseases, one gene. Report of the first Italian Meeting Course on Laminopathies

G. Boriani, G. Novelli, A. Pini, 2011, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.