Moyamoya syndrome in children with neurofibromatosis type 1: Italian–French experienceClaudia Santoro, Silverio Perrotta, Nathalie Boddaert et al.|American Journal of Medical Genetics Part A|2017Cited by 38
A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright ObjectsGaetano Terrone, Ennio Del Giudice, Giuseppina Vitiello et al.|European Journal of Paediatric Neurology|2017Cited by 5