Výsledky vyhledávání - "Federica Saia"

Akademický článek

Sensory phenomena in children with Tourette syndrome or autism spectrum disorder

Autor: Adriana Prato, Federica Saia, Marianna Ferrigno, Valentina Finocchiaro, Rita Barone, Renata Rizzo

Publikováno v: Frontiers in Psychiatry, Vol 15 (2024)

BackgroundTourette syndrome (TS) and autism spectrum disorder (ASD) are two neurodevelopmental disorders with an onset before the age of 18 years. TS patients frequently reported atypical sensory phenomena (SP). Sensory processing abnormalities are a

Externí odkaz: https://doaj.org/article/ecb52f6b31444b6d8ca0879a6f6a23dc

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Akademický článek

Symptoms compatible with long COVID in an Italian pediatric cohort of Tourette patients with and without SARS‑CoV‑2 infection: a short-term follow-up assessment

Autor: Adriana Prato, Angela Maria Salerno, Federica Saia, Nicoletta Maugeri, Alice Zanini, Miriam Scerbo, Rita Barone, Renata Rizzo

Publikováno v: BMC Pediatrics, Vol 23, Iss 1, Pp 1-10 (2023)

Abstract Background Tourette Syndrome (TS) is a childhood-onset neurodevelopmental disorder with a worldwide prevalence of about 0.3–1% of the population. During the pandemic caused by SARS-CoV-2 infection, the impact on the mental health of childr

Externí odkaz: https://doaj.org/article/486212da17274b75b709970c3d77cc1c

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Akademický článek

Functional tic-like behaviours during the COVID-19 pandemic: Follow-up over 12 months

Autor: Adriana Prato, Federica Saia, Maria Chiara Milana, Miriam Scerbo, Rita Barone, Renata Rizzo

Publikováno v: Frontiers in Pediatrics, Vol 10 (2023)

BackgroundFunctional tics are included in the wide spectrum of functional movement disorders (FMDs). Their distinction from organic tics is challenging because they both phenomenologically present common features. During the COVID-19 pandemic, there

Externí odkaz: https://doaj.org/article/d66a2fea14a143b3932c44482f23e220

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Akademický článek

Novel malformations: Chiari type 1 and hydrocephalus in Zhu‐Tokita‐Takenouchi‐Kim syndrome and novel SON variants

Autor: Piero Pavone, Federica Saia, Xena Pappalardo, Massimo Barbagallo, Adriana Prato, Renata Rizzo

Publikováno v: Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)

Abstract Zhu‐Tokita‐Tachenouchi‐Kim syndrome (ZTTK) is a recently recognized malformation syndrome presenting with craniofacial dysmorphism, developmental delay/intellectual disability, seizures, anomalies involving brain white matter, and othe

Externí odkaz: https://doaj.org/article/749d71e2659e4e26b93a85d8fac7d1cf

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Akademický článek

17q21.31 Microduplication Syndrome in a Patient with Autism Spectrum Disorder, Macrocephaly, and Intellectual Disability

Autor: Federica Saia, Adriana Prato, Caterina Angela Florio, Vincenzo Paolo Cutrone, Renata Rizzo

Publikováno v: Reports, Vol 6, Iss 3, p 30 (2023)

The chromosome 17q21.31 microduplication syndrome is a rare genetic syndrome presenting with craniofacial dysmorphisms, psychomotor delay, microcephaly, behavioral disorders, and poor social interaction. Only ten patients have been reported in the li

Externí odkaz: https://doaj.org/article/01c776534aa94bf38963892b8b380c6d

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Akademický článek

Enhancing neuroimaging genetics through meta-analysis for Tourette syndrome (ENIGMA-TS): A worldwide platform for collaboration

Autor: Peristera Paschou, Yin Jin, Kirsten Müller-Vahl, Harald E. Möller, Renata Rizzo, Pieter J. Hoekstra, Veit Roessner, Nanette Mol Debes, Yulia Worbe, Andreas Hartmann, Pablo Mir, Danielle Cath, Irene Neuner, Heike Eichele, Chencheng Zhang, Katarzyna Lewandowska, Alexander Munchau, Julius Verrel, Richard Musil, Tim J. Silk, Colleen A. Hanlon, Emily D. Bihun, Valerie Brandt, Andrea Dietrich, Natalie Forde, Christos Ganos, Deanna J. Greene, Chunguang Chu, Michel J. Grothe, Tamara Hershey, Piotr Janik, Jonathan M. Koller, Juan Francisco Martin-Rodriguez, Karsten Müller, Stefano Palmucci, Adriana Prato, Shukti Ramkiran, Federica Saia, Natalia Szejko, Renzo Torrecuso, Zeynep Tumer, Anne Uhlmann, Tanja Veselinovic, Tomasz Wolańczyk, Jade-Jocelyne Zouki, Pritesh Jain, Apostolia Topaloudi, Mary Kaka, Zhiyu Yang, Petros Drineas, Sophia I. Thomopoulos, Tonya White, Dick J. Veltman, Lianne Schmaal, Dan J. Stein, Jan Buitelaar, Barbara Franke, Odile van den Heuvel, Neda Jahanshad, Paul M. Thompson, Kevin J. Black

Publikováno v: Frontiers in Psychiatry, Vol 13 (2022)

Tourette syndrome (TS) is characterized by multiple motor and vocal tics, and high-comorbidity rates with other neuropsychiatric disorders. Obsessive compulsive disorder (OCD), attention deficit hyperactivity disorder (ADHD), autism spectrum disorder

Externí odkaz: https://doaj.org/article/4f62c0b936b04db99c17bdde6d51f583

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Akademický článek

Incidence of Autism Spectrum Disorder in Youths Affected by Gilles de la Tourette Syndrome Based on Data from a Large Single Italian Clinical Cohort

Autor: Mariangela Gulisano, Rita Barone, Maria Rita Mosa, Maria Chiara Milana, Federica Saia, Miriam Scerbo, Renata Rizzo

Publikováno v: Brain Sciences, Vol 10, Iss 11, p 812 (2020)

Gilles de la Tourette syndrome (GTS) and autism spectrum disorder (ASD) are etiologically related neurodevelopmental disorders with an onset age before 18 years and a reported comorbidity of 2.9–20%. The aim of the present study was to identify the

Externí odkaz: https://doaj.org/article/2143d06276ae46208e3aff6fa34baa04

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Copy Number Variations in Children with Tourette Syndrome: Systematic Investigation in a Clinical Setting

Autor: Federica Saia, Adriana Prato, Lucia Saccuzzo, Francesca Madia, Rita Barone, Marco Fichera, Renata Rizzo

Publikováno v: Genes
Volume 14
Issue 2
Pages: 500

Tourette syndrome (TS) is a neurodevelopmental disturbance with heterogeneous and not completely known etiology. Clinical and molecular appraisal of affected patients is mandatory for outcome amelioration. The current study aimed to understand the mo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbce3b4ff40c0c22cec5898726a1c028
https://doi.org/10.3390/genes14020500

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