Paolo Alfieri (P Alfieri)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 25

Top Topics

Tyrosine Kinase

Autism Spectrum Disorder

Psychometric Properties

Top Venues

American journal of medical genetics. Part C, Seminars in medical genetics

Journal of clinical medicine

Genes, brain, and behavior

This page only lists publications with an associated author ORCID identifier.

Publications

Federica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, Alessia Brunetti, Alessandra Airoldi, Anna de Florio, Luigi Tinella, Andrea Bosco, Stefano Vicari
Fragile X Syndrome and FMR1 premutation: results from a survey on associated conditions and treatment priorities in Italy. Orphanet journal of rare diseases 19 (1) (2024)
Federica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, Alessia Brunetti, Alessandra Airoldi, Anna de Florio, Luigi Tinella, Andrea Bosco, Stefano Vicari
Fragile X Syndrome and FMR1 premutation: results from a survey on associated conditions and treatment priorities in Italy. Orphanet journal of rare diseases 19 (1) (2024)
Federica Alice Maria Montanaro, Paolo Alfieri, Stefano Vicari
"Corp-Osa-Mente", a Combined Psychosocial-Neuropsychological Intervention for Adolescents and Young Adults with Fragile X Syndrome: An Explorative Study. Brain sciences 13 (2) (2023)
Alessandra Rossi, Lot Snijders Blok, Sonja Neuser, Chiara Klöckner, Konrad Platzer, Laurence Olivier Faivre, Heike Weigand, Maria Lisa Dentici, Tartaglia Marco, Marcello Niceta, Paolo Alfieri, Siddharth Srivastava, David Coulter, Lacey Smith, Kristin Vinorum, Gerarda Cappuccio, Nicola Brunetti-Pierri, Deniz Torun, Mutluay Arslan, Mathilde F Lauridsen, Oliver Murch, Rachel Irving, Sally A Lynch, Sarju G Mehta, Jenny Carmichael, Evelien Zonneveld-Huijssoon, Bert de Vries, Tjitske Kleefstra, Katrine M Johannesen, Ian T Westphall, Susan S Hughes, Sarah Smithson, Julie Evans, Tracy Dudding-Byth, Marleen Simon, Ellen van Binsbergen, Johanna C Herkert, Gea Beunders, Henry Oppermann, Mert Bakal, Rikke S Møller, Guido Rubboli, Allan Bayat
POU3F3-related disorder: Defining the phenotype and expanding the molecular spectrum. Clinical genetics (2023)
Federica Alice Maria Montanaro, Paolo Alfieri, Stefano Vicari
"Corp-Osa-Mente", a Combined Psychosocial-Neuropsychological Intervention for Adolescents and Young Adults with Fragile X Syndrome: An Explorative Study. Brain sciences 13 (2) (2023)
Federica Alice Maria Montanaro, Paolo Alfieri, Stefano Vicari
"Corp-Osa-Mente", a Combined Psychosocial-Neuropsychological Intervention for Adolescents and Young Adults with Fragile X Syndrome: An Explorative Study. Brain sciences 13 (2) (2023)
Domizia Pasquetti, Federica Francesca L'Erario, Giuseppe Marangi, Arianna Panfili, Pietro Chiurazzi, Elena Sonnini, Daniela Orteschi, Paolo Alfieri, null null, Manuela Morleo, Vincenzo Nigro, Marcella Zollino
Pathogenic variants in SOX11 mimicking Pitt-Hopkins syndrome phenotype. Clinical genetics (2023)
Federica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, Francesca Cumbo, Simone Piga, Tartaglia Marco, Serena Licchelli, Maria Cristina Digilio, Stefano Vicari
Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndrome. American journal of medical genetics. Part C, Seminars in medical genetics (2022)
Federica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, Francesca Cumbo, Simone Piga, Tartaglia Marco, Serena Licchelli, Maria Cristina Digilio, Stefano Vicari
Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndrome. American journal of medical genetics. Part C, Seminars in medical genetics 190 (4) (2022)
Federica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, Francesca Cumbo, Simone Piga, Tartaglia Marco, Serena Licchelli, Maria Cristina Digilio, Stefano Vicari
Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndrome. American journal of medical genetics. Part C, Seminars in medical genetics 190 (4) (2022)
Paolo Alfieri, Marina Macchiaiolo, Martina Collotta, Federica Alice Maria Montanaro, Cristina Caciolo, Francesca Cumbo, Paolo Galassi, Filippo Maria Panfili, Fabiana Cortellessa, Marcella Zollino, Maria Accadia, Marco Seri, Tartaglia Marco, Andrea Bartuli, Corrado Mammì, Stefano Vicari, Manuela Priolo
Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome. Journal of clinical medicine 11 (14) (2022)
Federica Alice Maria Montanaro, Paolo Alfieri, Cristina Caciolo, Francesca Cumbo, Simone Piga, Tartaglia Marco, Serena Licchelli, Maria Cristina Digilio, Stefano Vicari
Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndrome. American journal of medical genetics. Part C, Seminars in medical genetics 190 (4) (2022)
Francesco Demaria, Paolo Alfieri, Maria Cristina Digilio, Maria Pontillo, Cristina Di Vincenzo, Federica Alice Maria Montanaro, Valentina Ciullo, Giuseppe Zampino, Stefano Vicari
Obsessive Compulsive "Paper Handling": A Potential Distinctive Behavior in Children and Adolescents with KBG Syndrome. Journal of clinical medicine 11 (16) (2022)
Paolo Alfieri, Francesco Scibelli, Federica Alice Maria Montanaro, Maria Cristina Digilio, Lucilla Ravà, Giovanni Valeri, Stefano Vicari
Differences and Similarities in Adaptive Functioning between Children with Autism Spectrum Disorder and Williams-Beuren Syndrome: A Longitudinal Study. Genes 13 (7) (2022)
Paolo Alfieri, Cristina Caciolo, Giulia Lazzaro, Deny Menghini, Francesca Cumbo, Maria Lisa Dentici, Maria Cristina Digilio, Maria Gnazzo, Francesco Demaria, Virginia Pironi, Giuseppe Zampino, Antonio Novelli, Marco Tartaglia, Stefano Vicari
Cognitive and Adaptive Characterization of Children and Adolescents with KBG Syndrome: An Explorative Study. Journal of clinical medicine 10 (7) (2021)
Paolo Alfieri, Francesca Cumbo, Giulia Serra, Monia Trasolini, Camilla Frattini, Francesco Scibelli, Serena Licchelli, Flavia Cirillo, Cristina Caciolo, Maria Pia Casini, Adele D'Amico, Marco Tartaglia, Maria Cristina Digilio, Rossella Capolino, Stefano Vicari
Manic and Depressive Symptoms in Children Diagnosed with Noonan Syndrome. Brain sciences 11 (2) (2021)
Paolo Alfieri, Francesco Scibelli, Laura Casula, Simone Piga, Eleonora Napoli, Giovanni Valeri, Stefano Vicari
Cooperative Parent-Mediated Therapy in Children with Fragile X Syndrome and Williams Beuren Syndrome: A Pilot RCT Study of a Transdiagnostic Intervention-Preliminary Data. Brain sciences 12 (1) (2021)
Floriana Costanzo, Paolo Alfieri, Cristina Caciolo, Paola Bergonzini, Francesca Perrino, Giuseppe Zampino, Chiara Leoni, Deny Menghini, Maria Cristina Digilio, Marco Tartaglia, Stefano Vicari, Giovanni Augusto Carlesimo
Recognition Memory in Noonan Syndrome. Brain sciences 11 (2) (2021)
Paolo Alfieri, Francesco Scibelli, Maria C Digilio, Roberta L Novello, Cristina Caciolo, Giovanni Valeri, Stefano Vicari
Comparison of Adaptive Functioning in Children with Williams Beuren Syndrome and Autism Spectrum Disorder: A Cross-Syndrome Study. Autism research : official journal of the International Society for Autism Research 14 (4) (2020)
Giulia Lazzaro, Cristina Caciolo, Deny Menghini, Francesca Cumbo, Maria C Digilio, Rossella Capolino, Giuseppe Zampino, Marco Tartaglia, Stefano Vicari, Paolo Alfieri
Defining language disorders in children and adolescents with Noonan Syndrome. Molecular genetics & genomic medicine 8 (4) (2020)
Paolo Alfieri, Francesco Scibelli, Lorenzo Sinibaldi, Giovanni Valeri, Cristina Caciolo, Roberta Lucia Novello, Antonio Novelli, Maria Cristina Digilio, Marco Tartaglia, Stefano Vicari
Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases. Genes, brain, and behavior 19 (7) (2020)
Maria Lisa Dentici, Paola Bergonzini, Francesco Scibelli, Cristina Caciolo, Paola De Rose, Francesca Cumbo, Viola Alesi, Rossella Capolino, Ginevra Zanni, Lorenzo Sinibaldi, Antonio Novelli, Marco Tartaglia, Maria Cristina Digilio, Bruno Dallapiccola, Stefano Vicari, Paolo Alfieri
7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling. Brain sciences 10 (11) (2020)
Cristina Caciolo, Paolo Alfieri, Giorgia Piccini, Maria Cristina Digilio, Francesca Romana Lepri, Marco Tartaglia, Deny Menghini, Stefano Vicari
Neurobehavioral features in individuals with Kabuki syndrome. Molecular genetics & genomic medicine 6 (3) (2018)
Paolo Alfieri, D Menghini, L Marotta, L De Peppo, L Ravà, F Salvaguardia, C Varuzza, S Vicari
A comparison between linguistic skills and socio-communicative abilities in Williams syndrome. Journal of intellectual disability research : JIDR 61 (9) (2017)
G Piccini, D Menghini, A D'Andrea, C Caciolo, M Pontillo, M Armando, F Perrino, L Mandolesi, A Salerni, L Buzzonetti, M C Digilio, G Zampino, M Tartaglia, M Benassi, S Vicari, Paolo Alfieri
Visual perception skills: a comparison between patients with Noonan syndrome and 22q11.2 deletion syndrome. Genes, brain, and behavior 16 (6) (2017)