Francesca Gualandi

GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann et al. · The American Journal of Human Genetics · 2005 · 559 citations · Full text

Medicine, Genetics, Otolaryngology +12

Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins

Alessia Angelin, Tania Tiepolo, Patrizia Sabatelli et al. · Proceedings of the National Academy of Sciences · 2007 · 187 citations · Full text

Life Sciences, Cell Biology, Pathobiology +17

Attention Deficit Hyperactivity Disorder and Cognitive Function in Duchenne Muscular Dystrophy: Phenotype-Genotype Correlation

Marika Pane, Maria Elena Lombardo, Paolo Alfieri et al. · The Journal of Pediatrics · 2012 · 175 citations

Medicine, Neurology, Neuroscience +15

A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield

Arunkanth Ankala, Cristina da Silva, Francesca Gualandi et al. · Annals of Neurology · 2014 · 167 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human

Marcella Neri, Silvia Torelli, I. Ugo et al. · Neuromuscular Disorders · 2007 · 166 citations

Medicine, Neurology, Neuromuscular Disorders +7