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Adolescents at ultra-high risk for psychosis with and without 22q11 deletion syndrome: a comparison of prodromal psychotic symptoms and general functioning.
Armando M, Girardi P, Vicari S, Menghini D, Digilio MC, Pontillo M, Saba R, Mazzone L, Lin A, Klier CM, Schäfer MR, Amminger GP. Armando M, et al. Among authors: digilio mc. Schizophr Res. 2012 Aug;139(1-3):151-6. doi: 10.1016/j.schres.2012.04.020. Epub 2012 May 23. Schizophr Res. 2012. PMID: 22627123
Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations.
Lo-Castro A, Brancati F, Digilio MC, Garaci FG, Bollero P, Alfieri P, Curatolo P. Lo-Castro A, et al. Among authors: digilio mc. Am J Med Genet B Neuropsychiatr Genet. 2013 Jan;162B(1):17-23. doi: 10.1002/ajmg.b.32113. Epub 2012 Nov 26. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23184435
Behavioral profile in RASopathies.
Alfieri P, Piccini G, Caciolo C, Perrino F, Gambardella ML, Mallardi M, Cesarini L, Leoni C, Leone D, Fossati C, Selicorni A, Digilio MC, Tartaglia M, Mercuri E, Zampino G, Vicari S. Alfieri P, et al. Among authors: digilio mc. Am J Med Genet A. 2014 Apr;164A(4):934-42. doi: 10.1002/ajmg.a.36374. Epub 2014 Jan 23. Am J Med Genet A. 2014. PMID: 24458522
Indicated prevention with long-chain polyunsaturated omega-3 fatty acids in patients with 22q11DS genetically at high risk for psychosis. Protocol of a randomized, double-blind, placebo-controlled treatment trial.
Armando M, De Crescenzo F, Vicari S, Digilio MC, Pontillo M, Papaleo F, Amminger GP. Armando M, et al. Among authors: digilio mc. Early Interv Psychiatry. 2016 Oct;10(5):390-6. doi: 10.1111/eip.12197. Epub 2014 Oct 24. Early Interv Psychiatry. 2016. PMID: 25345540 Clinical Trial.
Behavioral phenotype in Costello syndrome with atypical mutation: a case report.
Alfieri P, Caciolo C, Piccini G, D'Elia L, Valeri G, Menghini D, Tartaglia M, Digilio MC, Dallapiccola B, Vicari S. Alfieri P, et al. Among authors: digilio mc. Am J Med Genet B Neuropsychiatr Genet. 2015 Jan;168B(1):66-71. doi: 10.1002/ajmg.b.32279. Epub 2014 Nov 4. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 25367099
Visual perception skills: a comparison between patients with Noonan syndrome and 22q11.2 deletion syndrome.
Piccini G, Menghini D, D'Andrea A, Caciolo C, Pontillo M, Armando M, Perrino F, Mandolesi L, Salerni A, Buzzonetti L, Digilio MC, Zampino G, Tartaglia M, Benassi M, Vicari S, Alfieri P. Piccini G, et al. Among authors: digilio mc. Genes Brain Behav. 2017 Jul;16(6):627-634. doi: 10.1111/gbb.12381. Epub 2017 May 23. Genes Brain Behav. 2017. PMID: 28378436 Free article.
Psychopathological features in Noonan syndrome.
Perrino F, Licchelli S, Serra G, Piccini G, Caciolo C, Pasqualetti P, Cirillo F, Leoni C, Digilio MC, Zampino G, Tartaglia M, Alfieri P, Vicari S. Perrino F, et al. Among authors: digilio mc. Eur J Paediatr Neurol. 2018 Jan;22(1):170-177. doi: 10.1016/j.ejpn.2017.09.009. Epub 2017 Sep 28. Eur J Paediatr Neurol. 2018. PMID: 29037749
Clinical and Neurobehavioral Features of Three Novel Kabuki Syndrome Patients with Mosaic KMT2D Mutations and a Review of Literature.
Lepri FR, Cocciadiferro D, Augello B, Alfieri P, Pes V, Vancini A, Caciolo C, Squeo GM, Malerba N, Adipietro I, Novelli A, Sotgiu S, Gherardi R, Digilio MC, Dallapiccola B, Merla G. Lepri FR, et al. Among authors: digilio mc. Int J Mol Sci. 2017 Dec 28;19(1):82. doi: 10.3390/ijms19010082. Int J Mol Sci. 2017. PMID: 29283410 Free PMC article.
435 results