E Solla

A genome screen for multiple sclerosis in Sardinian multiplex families

Francesca Coraddu, Stephen Sawcer, Sandra D’Alfonso et al. · European Journal of Human Genetics · 2001 · 98 citations

Life Sciences, Genetics, Neurology +9

Overlapping syndromes in laminopathies: a meta-analysis of the reported literature.

Nicola Carboni, Luisa Politano, Matteo Floris et al. · PubMed · 2013 · 44 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Muscle imaging analogies in a cohort of patients with different clinical phenotypes caused by <i>LMNA</i> gene mutations

Nicola Carboni, Marco Mura, Giovanni Marrosu et al. · Muscle & Nerve · 2009 · 44 citations

Medicine, Genetics, Molecular Genetics +15

Dilated cardiomyopathy with conduction defects in a patient with partial merosin deficiency due to mutations in the laminin‐α2‐chain gene: A chance association or a novel phenotype?

Nicola Carboni, Giovanni Marrosu, Maurizio Porcu et al. · Muscle & Nerve · 2011 · 36 citations

Medicine, Cardiology, Genetics +17

Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation

Nicola Carboni, Marco Mura, Giovanni Marrosu et al. · Neuromuscular Disorders · 2008 · 30 citations

Medicine, Genetics, Molecular Genetics +15