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 · 551 citations · Full text

Genetic Disorder, Genetics, Audiology +9

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 · 184 citations · Full text

Mitochondrial Myopathy, Mechanobiology, Muscle Pathology +13

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 · 169 citations

Adhd, Duchenne Muscular Dystrophy, Phenotype-genotype Correlation +7

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 · 166 citations · Full text

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

Marcella Neri, Silvia Torelli, S. Brown et al. · Neuromuscular Disorders · 2007 · 163 citations

Urology, Kinesiology, Degenerative Disease +2