A. Lo‐Castro

Detecting anxiety symptoms in children and youths with neurofibromatosis type I

A. Pasini, M. Pitzianti, Martina Siracusano, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

ADHD and genetic syndromes

P. Curatolo, Elisa D'agati, A. Lo-Castro, 2011, Brain and Development.

Review article ADHD and genetic syndromes

P. Curatolo, A. Lo-Castro, A. Lo‐Castro, 2011 .

Epilepsy associated with autism and attention deficit hyperactivity disorder: Is there a genetic link?

P. Curatolo, A. Lo-Castro, A. Lo‐Castro, 2014, Brain and Development.

Association of Syndromic Mental Retardation and Autism with 22q11.2 Duplication

S. Benedetti, P. Curatolo, A. Nardone, 2009, Neuropediatrics.

Neurologic aspects of microcephalic osteodysplastic primordial dwarfism type II.

P. Curatolo, C. Cerminara, C. Galasso, 2008, Pediatric neurology.

De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems.

P. Curatolo, A. Verrotti, A. Nardone, 2011, European journal of medical genetics.

Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations

F. Garaci, M. Digilio, F. Brancati, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mild Wolf–Hirschhorn phenotype in a girl with unbalanced t(4p;12p) translocation without seizures

P. Curatolo, D. Orteschi, M. Zollino, 2010, American journal of medical genetics. Part A.

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome

A. Pagnamenta, A. Battaglia, D. Keays, 2015, Journal of Medical Genetics.

Late-Onset Epileptic Spasms in Children With Pallister-Killian Syndrome: A Report of Two New Cases and Review of the Electroclinical Aspects

M. Brinciotti, P. Curatolo, C. Cerminara, 2010, Journal of child neurology.