IRIS

Sfoglia per Autore  SACCO, ROBERTO

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Mostrati risultati da 1 a 20 di 37
Titolo Data di pubblicazione Autore(i) File
Laparoscopic transperitoneal right adrenalectomy for 'large' tumors 1-gen-2008 Papalia, R; Simone, G; Leonardo, C; Loreto, A; Coppola, R; Guaglianone, S; Sacco, R; Gallucci, M
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression 1-gen-2009 Lintas, C; Sacco, R; Garbett, K; Mirnics, K; Militerni, R; Bravaccio, C; Curatolo, P; Manzi, B; Schneider, C; Melmed, R; Elia, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, K-L; Persico, A M
The use of pegylated liposomal doxorubicin with hyperthermic intraperitoneal chemotherapy (HIPEC) in patients undergoing cytoreductive surgery (CS) for peritoneal carcinomatosis of ovarian origin 1-gen-2010 De Tursi, M; Salvatorelli, E; Carella, C; Bianco, N; Massari, R; Sacco, R; Menna, P; Minotti, G; Iacobelli, S
Decreased serum arylesterase activity in autism spectrum disorders 1-gen-2010 Gaita, Laura; Manzi, Barbara; Sacco, Roberto; Lintas, Carla; Altieri, Laura; Lombardi, Federica; Pawlowski, Tracy L; Redman, Margot; Craig, David W; Huentelman, Matthew J; Ober-Reynolds, Sharman; Brautigam, Sarah; Melmed, Raun; Smith, Christopher J; Marsillach, Judith; Camps, Jordi; Curatolo, Paolo; Persico, Antonio M
Association of autism with polyomavirus infection in postmortem brains 1-gen-2010 Lintas, Carla; Altieri, Laura; Lombardi, Federica; Sacco, Roberto; Persico, Antonio M
Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome 1-gen-2012 Lintas, Carla; Sacco, Roberto; Persico, Antonio M
Autism genetics: Methodological issues and experimental design 1-gen-2015 Sacco, Roberto; Lintas, Carla; Persico, Antonio M
Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features 1-gen-2016 Lintas, Carla; Picinelli, Chiara; Piras, Ignazio S; Sacco, Roberto; Gabriele, Stefano; Verdecchia, Magda; Persico, Antonio M
Differential methylation at the RELN gene promoter in temporal cortex from autistic and typically developing post-puberal subjects 1-gen-2016 Lintas, Carla; Sacco, Roberto; Persico, Antonio M
Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders 1-gen-2016 Picinelli, Chiara; Lintas, Carla; Piras, Ignazio Stefano; Gabriele, Stefano; Sacco, Roberto; Brogna, Claudia; Persico, Antonio Maria
Copy number variation in 19 Italian multiplex families with autism spectrum disorder: Importance of synaptic and neurite elongation genes 1-gen-2017 Lintas, Carla; Picinelli, Chiara; Piras, Ignazio Stefano; Sacco, Roberto; Brogna, Claudia; Persico, Antonio M
An Interstitial 17q11.2 de novo Deletion Involving the CDK5R1 Gene in a High-Functioning Autistic Patient 1-gen-2019 Lintas, Carla; Sacco, Roberto; Tabolacci, Claudio; Brogna, Claudia; Canali, Marco; Picinelli, Chiara; Tomaiuolo, Pasquale; Castronovo, Paola; Baccarin, Marco; Persico, Antonio M
Evidence that ITGB3 promoter variants increase serotonin blood levels by regulating platelet serotonin transporter trafficking 1-gen-2019 Gabriele, Stefano; Canali, Marco; Lintas, Carla; Sacco, Roberto; Tirindelli, Maria Cristina; Ricciardello, Arianna; Persico, Antonio M
Huntingtin gene CAG repeat size affects autism risk: Family-based and case–control association study 1-gen-2020 Piras, I. S.; Picinelli, C.; Iennaco, R.; Baccarin, M.; Castronovo, P.; Tomaiuolo, P.; Cucinotta, F.; Ricciardello, A.; Turriziani, L.; Nanetti, L.; Mariotti, C.; Gellera, C.; Lintas, C.; Sacco, R.; Zuccato, C.; Cattaneo, E.; Persico, A. M.
Smartphone and tablet addiction among children: A significant predictor of behavioral and physical alterations 1-gen-2020 Ferrara, P.; Infantino, C.; Franceschini, G.; Sacco, R.
Appropriateness of array-CGH in the ADHD clinics: A comparative study 1-gen-2020 Baccarin, Marco; Picinelli, Chiara; Tomaiuolo, Pasquale; Castronovo, Paola; Costa, Anna; Verdecchia, Magda; Cannizzaro, Chiara; Barbieri, Giusi; Sacco, Roberto; Persico, Antonio M; Lintas, Carla
Genetic and epigenetic MTHFR gene variants in the mothers of attention-deficit/hyperactivity disorder affected children as possible risk factors for neurodevelopmental disorders 1-gen-2020 Piras, Ignazio Stefano; Costa, Anna; Tirindelli, Maria Cristina; Stoccoro, Andrea; Huentelman, Matthew J; Sacco, Roberto; Coppedè, Fabio; Lintas, Carla
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family 1-gen-2020 Cucinotta, Francesca; Ricciardello, Arianna; Turriziani, Laura; Calabrese, Giorgia; Briguglio, Marilena; Boncoddo, Maria; Bellomo, Fabiana; Tomaiuolo, Pasquale; Martines, Silvia; Bruschetta, Marianna; La Fauci Belponer, Francesca; Di Bella, Tiziana; Colombi, Costanza; Baccarin, Marco; Picinelli, Chiara; Castronovo, Paola; Lintas, Carla; Sacco, Roberto; Biederer, Thomas; Kellam, Barbara; Scherer, Stephen W; Persico, Antonio M
Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review 1-gen-2020 Castronovo, Paola; Baccarin, Marco; Ricciardello, Arianna; Picinelli, Chiara; Tomaiuolo, Pasquale; Cucinotta, Francesca; Frittoli, Myriam; Lintas, Carla; Sacco, Roberto; Persico, Antonio M
Reevaluation of serum arylesterase activity in neurodevelopmental disorders 1-gen-2021 Piras, I. S.; Gabriele, S.; Altieri, L.; Lombardi, F.; Sacco, R.; Lintas, C.; Manzi, B.; Curatolo, P.; Nobile, M.; Rigoletto, C.; Molteni, M.; Persico, A. M.
Mostrati risultati da 1 a 20 di 37
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