Caterina Zanus

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

Francesca Clementina Radio, Kaifang Pang, Andrea Ciolfi et al. · The American Journal of Human Genetics · 2021 · 90 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Paediatric anti-N-methyl-d-aspartate receptor encephalitis: The first Italian multicenter case series

Stefano Sartori, Margherita Nosadini, Elisabetta Cesaroni et al. · European Journal of Paediatric Neurology · 2015 · 59 citations

Medicine, Neurology, Pediatrics +10

Defining the electroclinical phenotype and outcome of PCDH19‐related epilepsy: A multicenter study

Marina Trivisano, Nicola Pietrafusa, Carla Marini et al. · Epilepsia · 2018 · 53 citations · Full text

Medicine, Genetics, Neurology +17

Diagnostic criteria currently proposed for “ictal epileptic headache”: Perspectives on strengths, weaknesses and pitfalls

Pasquale Parisi, Alberto Verrotti, Paola Costa et al. · Seizure · 2015 · 52 citations · Full text

Medicine, Neurology, Neuroscience +13

Adolescent Admissions to Emergency Departments for Self-Injurious Thoughts and Behaviors

Caterina Zanus, Sara Battistutta, Renata Aliverti et al. · PLoS ONE · 2017 · 35 citations · Full text

Medicine, Emergency Medicine, Pediatrics +14