Roberta Paravidino

Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance

Federico Zara, Nicola Specchio, Pasquale Striano et al. · Epilepsia · 2013 · 122 citations · Full text

PRRT2 Mutations are the major cause of benign familial infantile seizures

Julian Schubert, Roberta Paravidino, Felicitas Becker et al. · Human Mutation · 2012 · 104 citations

Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype–Phenotype Correlations

Pasquale Striano, Maria Margherita Mancardi, Roberta Biancheri et al. · Epilepsia · 2007 · 92 citations · Full text

Cryptic chromosome deletions involving <i>SCN1A</i> in severe myoclonic epilepsy of infancy

Francesca Madia, Pasquale Striano, Elena Di Gennaro et al. · Neurology · 2006 · 79 citations

Loss‐of‐function <i><scp>KCNH</scp>2</i> mutation in a family with long <scp>QT</scp> syndrome, epilepsy, and sudden death

Sara Partemi, Sandrine Cestèle, Marianna Pezzella et al. · Epilepsia · 2013 · 67 citations