A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes

por Nardello, Rosaria, Antona, Vincenzo, Mangano, Giuseppe Donato, Salpietro, Vincenzo, Mangano, Salvatore, Fontana, Antonina
Publicado 2021

West syndrome followed by juvenile myoclonic epilepsy: a coincidental occurrence?

por Mangano, Salvatore, Nardello, Rosaria, Tripi, Gabriele, Giordano, Giuliana, Spitaleri, Chiara, Mangano, Giuseppa Renata, Fontana, Antonina
Publicado 2013

Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review

por Mangano, Giuseppe Donato, Fontana, Antonina, Antona, Vincenzo, Salpietro, Vincenzo, Mangano, Giuseppa Renata, Giuffrè, Mario, Nardello, Rosaria
Publicado 2022

Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant

por Nardello, Rosaria, Plicato, Giorgia, Mangano, Giuseppe Donato, Gennaro, Elena, Mangano, Salvatore, Brighina, Filippo, Raieli, Vincenzo, Fontana, Antonina
Publicado 2020