Laura Valentina Renna

Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2

Rosanna Cardani, Marzia Giagnacovo, Annalisa Botta et al. · Journal of Neurology · 2012 · 49 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +7

Overexpression of CUGBP1 in Skeletal Muscle from Adult Classic Myotonic Dystrophy Type 1 but Not from Myotonic Dystrophy Type 2

Rosanna Cardani, Enrico Bugiardini, Laura Valentina Renna et al. · PLoS ONE · 2013 · 42 citations · Full text

Muscle Function, Genetics, Pathology +18

Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1

Christine Voellenkle, Alessandra Perfetti, Matteo Carrara et al. · International Journal of Molecular Sciences · 2019 · 40 citations · Full text

Receptor and post-receptor abnormalities contribute to insulin resistance in myotonic dystrophy type 1 and type 2 skeletal muscle

Laura Valentina Renna, Francesca Bosè, Sara Iachettini et al. · PLoS ONE · 2017 · 38 citations · Full text

Muscle Function, Insulin Receptor, Insulin Signaling +20

Premature senescence in primary muscle cultures of myotonic dystrophy type 2 is not associated with p16 induction

Laura Valentina Renna, Rosanna Cardani, Annalisa Botta et al. · European Journal of Histochemistry · 2014 · 33 citations · Full text

Fibre Atrophy, Muscle Function, Cellular Physiology +17