Adriana Lo‐Castro

发表

Sox11 Is Required to Maintain Proper Levels of Hedgehog Signaling during Vertebrate Ocular Morphogenesis

M. Fichera, O. Lehmann, S. Musumeci, 2014, PLoS genetics.

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.

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.

"Idiopathic" mental retardation and new chromosomal abnormalities

P. Curatolo, C. Galasso, A. Lo-Castro, 2010, Italian journal of pediatrics.

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.

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.

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.

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

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

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.

Deletion 2q37: An Identifiable Clinical Syndrome With Mental Retardation and Autism

P. Curatolo, A. Nardone, F. Gullotta, 2008, Journal of child neurology.

Neuroimaging findings of Sturge–Weber Syndrome in a child with Tuberous Sclerosis

P. Curatolo, R. Moavero, R. Bombardieri, 2009, Brain and Development.

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 .

Autism spectrum disorders associated with chromosomal abnormalities

P. Curatolo, C. Galasso, A. Lo-Castro, 2010 .

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.

Planning Deficit in Children With Neurofibromatosis Type 1

P. Curatolo, Elisa D'agati, A. Pasini, 2014, Journal of child neurology.