Maria Pintaudi

Epilepsy in Rett syndrome: Clinical and genetic features

Maria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli et al. · Epilepsy & Behavior · 2010 · 82 citations · Full text

Medicine, Genetics, Neurology +14

Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes

Silvia Russo, Margherita Marchi, Francesca Cogliati et al. · Neurogenetics · 2009 · 71 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

West syndrome associated with 14q12 duplications harboring FOXG1

Pasquale Striano, Roberta Paravidino, Federico Sicca et al. · Neurology · 2011 · 55 citations

Life Sciences, Genetics, Neurology +15

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases

Pasquale Striano, Michela Malacarne, Simona Cavani et al. · American Journal of Medical Genetics Part A · 2006 · 52 citations

Life Sciences, Genetics, Molecular Genetics +15

Analysis of the Phenotypes in the Rett Networked Database

Elisa Frullanti, Filomena Tiziana Papa, Elisa Grillo et al. · International Journal of Genomics · 2019 · 48 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15