Giuliana Galluzzi

Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

Marina Raffaele di Barletta, Enzo Ricci, Giuliana Galluzzi et al. · The American Journal of Human Genetics · 2000 · 411 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype

Enzo Ricci, Giuliana Galluzzi, Giancarlo Deidda et al. · Annals of Neurology · 1999 · 296 citations

Ecori Fragment Size, Rare Diseases, Facioscapulohumeral Muscular Dystrophy +15

Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression

Mario Pescatori, Aldobrando Broccolini, Carlo Minetti et al. · The FASEB Journal · 2007 · 244 citations

Muscle Function, Engineering, Genetics +17

Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north‐east Italian population sample

ML Mostacciuolo, Ebe Pastorello, Giovanni Vazza et al. · Clinical Genetics · 2009 · 156 citations

Facioscapulohumeral Muscular Dystrophy, Mendelian Disorder, Fshd Patients +13

A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score

Costanza Lamperti, Greta Fabbri, Liliana Vercelli et al. · Muscle & Nerve · 2010 · 151 citations · Full text

Muscle Function, Diagnosis, Orthopaedic Surgery +17