Giulio Piluso

Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene

Vincenzo Nigro, Eloisa De Sá Moreira, Giulio Piluso et al. · Nature Genetics · 1996 · 421 citations

Rare Diseases, Mendelian Disorder, Genetic Disorder +8

Improvement of survival in Duchenne Muscular Dystrophy: retrospective analysis of 835 patients.

Luigia Passamano, Antonella Taglia, Alberto Palladino et al. · PubMed · 2012 · 326 citations · Full text

Heart Failure, Pediatric Heart Disease, Retrospective Analysis +16

Gentamicin administration in Duchenne patients with premature stop codon. Preliminary results.

Luisa Politano, Gerardo Nigro, Vincenzo Nigro et al. · PubMed · 2003 · 172 citations

Duchenne Patients, Translational Medicine, Premature Stop Codon +13

Clinical spectrum of individuals with pathogenic <i> <b>N</b> F1 </i> missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1

Magdalena Koczkowska, Tom Callens, Yunjia Chen et al. · Human Mutation · 2019 · 130 citations · Full text

Interaction of Vault Particles with Estrogen Receptor in the MCF-7 Breast Cancer Cell

Ciro Abbondanza, Valentina Rossi, Annarita Roscigno et al. · The Journal of Cell Biology · 1998 · 125 citations · Full text