Federica Alice Maria Montanaro

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 18

Top Topics

Autism Spectrum Disorder

Psychometric Properties

Placebo Controlled

Parkinson Disease

Top Venues

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

Journal of clinical medicine

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

Publications

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)
Ellery Santos, Courtney Clark, Hazel Maridith B Biag, Si Jie Tang, Kyoungmi Kim, Matthew D Ponzini, Andrea Schneider, Cecilia Giulivi, Federica Alice Maria Montanaro, Jesse Tran-Emilia Gipe, Jacquelyn Dayton, Jamie L Randol, Pamela J Yao, Apostolos Manolopoulos, Dimitrios Kapogiannis, Ye Hyun Hwang, Paul Hagerman, Randi J Hagerman, Flora Tassone
Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS). Cells 12 (24) (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)
Ellery Santos, Courtney Clark, Hazel Maridith B Biag, Si Jie Tang, Kyoungmi Kim, Matthew D Ponzini, Andrea Schneider, Cecilia Giulivi, Federica Alice Maria Montanaro, Jesse Tran-Emilia Gipe, Jacquelyn Dayton, Jamie L Randol, Pamela J Yao, Apostolos Manolopoulos, Dimitrios Kapogiannis, Ye Hyun Hwang, Paul Hagerman, Randi J Hagerman, Flora Tassone
Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS). Cells 12 (24) (2023)
Ellery Santos, Courtney Clark, Hazel Maridith B Biag, Si Jie Tang, Kyoungmi Kim, Matthew D Ponzini, Andrea Schneider, Cecilia Giulivi, Federica Alice Maria Montanaro, Jesse Tran-Emilia Gipe, Jacquelyn Dayton, Jamie L Randol, Pamela J Yao, Apostolos Manolopoulos, Dimitrios Kapogiannis, Ye Hyun Hwang, Paul Hagerman, Randi J Hagerman, Flora Tassone
Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS). Cells 12 (24) (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)
Ellery Santos, Courtney Clark, Hazel Maridith B Biag, Si Jie Tang, Kyoungmi Kim, Matthew D Ponzini, Andrea Schneider, Cecilia Giulivi, Federica Alice Maria Montanaro, Jesse Tran-Emilia Gipe, Jacquelyn Dayton, Jamie L Randol, Pamela J Yao, Apostolos Manolopoulos, Dimitrios Kapogiannis, Ye Hyun Hwang, Paul Hagerman, Randi J Hagerman, Flora Tassone
Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS). Cells 12 (24) (2023)
Ellery Santos, Courtney Clark, Hazel Maridith B Biag, Si Jie Tang, Kyoungmi Kim, Matthew D Ponzini, Andrea Schneider, Cecilia Giulivi, Federica Alice Maria Montanaro, Jesse Tran-Emilia Gipe, Jacquelyn Dayton, Jamie L Randol, Pamela J Yao, Apostolos Manolopoulos, Dimitrios Kapogiannis, Ye Hyun Hwang, Paul Hagerman, Randi J Hagerman, Flora Tassone
Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS). Cells 12 (24) (2023)
Ellery Santos, Courtney Clark, Hazel Maridith B Biag, Si Jie Tang, Kyoungmi Kim, Matthew D Ponzini, Andrea Schneider, Cecilia Giulivi, Federica Alice Maria Montanaro, Jesse Tran-Emilia Gipe, Jacquelyn Dayton, Jamie L Randol, Pamela J Yao, Apostolos Manolopoulos, Dimitrios Kapogiannis, Ye Hyun Hwang, Paul Hagerman, Randi J Hagerman, Flora Tassone
Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS). Cells 12 (24) (2023)
Flora Tassone, Dragana D Protic, Emily Graves Allen, Alison Dalton Archibald, Anna Baud, Ted W Brown, Dejan B Budimirovic, Jonathan Cohen, Brett Dufour, Rachel Eiges, Nicola Elvassore, Lidia V Gabis, Samantha J Grudzien, Deborah A Hall, David R Hessl, Abigail Hogan, Jessica Ezzell Hunter, Peng Jin, Poonnada Jiraanont, Jessica Klusek, R Frank Kooy, Claudine M Kraan, Cecilia Laterza, Andrea Lee, Karen Lipworth, Molly Losh, Danuta Z Loesch, Reymundo Lozano, Marsha R Mailick, Apostolos Manolopoulos, Veronica Martinez-Cerdeno, Yingratana McLennan, Robert M Miller, Federica Alice Maria Montanaro, Matthew W Mosconi, Sarah Nelson Potter, Melissa Raspa, Susan M Rivera, Katharine Shelly, Peter K Todd, Katarzyna Tutak, Jun Yi Wang, Anne Wheeler, Tri Indah Winarni, Marwa Zafarullah, Randi J Hagerman
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation. Cells 12 (18) (2023)
Ellery Santos, Courtney Clark, Hazel Maridith B Biag, Si Jie Tang, Kyoungmi Kim, Matthew D Ponzini, Andrea Schneider, Cecilia Giulivi, Federica Alice Maria Montanaro, Jesse Tran-Emilia Gipe, Jacquelyn Dayton, Jamie L Randol, Pamela J Yao, Apostolos Manolopoulos, Dimitrios Kapogiannis, Ye Hyun Hwang, Paul Hagerman, Randi J Hagerman, Flora Tassone
Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS). Cells 12 (24) (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)