V.M. Ventriglia

Molecular diagnosis in LGMD2A: Mutation analysis or protein testing?

Luigi Fulizio, A. Nascimbeni, Marco Spinazzi et al. · Human Mutation · 2004 · 113 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery–Dreifuss muscular dystrophy

Gerardo Nigro, Vincenzo Russo, V.M. Ventriglia et al. · Neuromuscular Disorders · 2010 · 37 citations

Medicine, Cardiology, Neurology +14

Corneal Thickness and Endothelial Cell Characteristics in Patients with Myotonic Dystrophy

Nicola Rosa, Michele Lanza, Maria Borrelli et al. · Ophthalmology · 2009 · 31 citations

Medicine, Ophthalmology, Optometry +15

Log-PCR: A New Tool for Immediate and Cost-Effective Diagnosis of up to 85% of Dystrophin Gene Mutations

Amelia Trimarco, Annalaura Torella, Giulio Piluso et al. · Clinical Chemistry · 2008 · 22 citations · Full text

Medicine, Genetics, Molecular Genetics +13