Cristina Petrelli

Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutations

Valentina Cetica, Sara Chiari, Davide Mei et al. · Neurology · 2017 · 132 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Association of Variants in the <i>SPTLC1</i> Gene With Juvenile Amyotrophic Lateral Sclerosis

Janel O. Johnson, Ruth Chia, Danny E. Miller et al. · JAMA Neurology · 2021 · 84 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

DNA vaccination with full-length or truncated Neu induces protective immunity against the development of spontaneous mammary tumors in HER-2/neu transgenic mice

Augusto Amici, Arianna Smorlesi, Giuseppe Noce et al. · Gene Therapy · 2000 · 68 citations

Medicine, Immunology, Oncology +17

Variable epilepsy phenotypes associated with a familial intragenic deletion of the <i>SCN1A</i> gene

Renzo Guerrini, Elena Cellini, Davide Mei et al. · Epilepsia · 2010 · 65 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Vagus Nerve Stimulation for Refractory Epilepsy in Tuberous Sclerosis

Nelia Zamponi, Cristina Petrelli, Claudia Passamonti et al. · Pediatric Neurology · 2010 · 56 citations

Medicine, Neurology, Neuroscience +16