Zobrazeno 1 - 10
of 1 234
pro vyhledávání: '"M, Persico"'
Autor:
Lisa Asta, Arianna Ricciardello, Francesca Cucinotta, Laura Turriziani, Maria Boncoddo, Fabiana Bellomo, Jessica Angelini, Martina Gnazzo, Giulia Scandolo, Giulia Pisanò, Francesco Pelagatti, Fethia Chehbani, Michela Camia, Antonio M. Persico
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-24 (2024)
Abstract Background Phelan-McDermid syndrome (PMS) is caused by monoallelic loss or inactivation at the SHANK3 gene, located in human chr 22q13.33, and is often associated with Autism Spectrum Disorder (ASD). Objectives To assess the clinical and dev
Externí odkaz:
https://doaj.org/article/8b092706895e4762b4e869959cc80894
Autor:
Lisa Asta, Tiziana Di Bella, Francesca La Fauci Belponer, Marianna Bruschetta, Silvia Martines, Enrica Basile, Maria Boncoddo, Fabiana Bellomo, Francesca Cucinotta, Arianna Ricciardello, Laura Turriziani, Costanza Colombi, Federico Banchelli, Riccardo Cuoghi Costantini, Roberto D’Amico, Antonio M. Persico
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
IntroductionThe effectiveness of early interventions in young autistic children is well established, but there is great interindividual variability in treatment response. Predictors of response to naturalistic developmental behavioral interventions (
Externí odkaz:
https://doaj.org/article/c50f5eba7ab5444a8e159b4b634c0e26
Autor:
Laura Lombardi, Sigrid Le Clerc, Ching-Lien Wu, Jihène Bouassida, Wahid Boukouaci, Sobika Sugusabesan, Jean-Romain Richard, Mohamed Lajnef, Maxime Tison, Philippe Le Corvoisier, Caroline Barau, Tobias Banaschewski, Rosemary Holt, Sarah Durston, Antonio M. Persico, Bethany Oakley, Eva Loth, Jan Buitelaar, Declan Murphy, Marion Leboyer, Jean-François Zagury, Ryad Tamouza
Publikováno v:
Translational Psychiatry, Vol 13, Iss 1, Pp 1-13 (2023)
Abstract Autism spectrum disorders (ASD) are neurodevelopmental conditions that are for subsets of individuals, underpinned by dysregulated immune processes, including inflammation, autoimmunity, and dysbiosis. Consequently, the major histocompatibil
Externí odkaz:
https://doaj.org/article/ae3e3409be1844129fafe8a901016542
Autor:
Pasquale Tomaiuolo, Ignazio Stefano Piras, Simona Baghai Sain, Chiara Picinelli, Marco Baccarin, Paola Castronovo, Marco J. Morelli, Dejan Lazarevic, Maria Luisa Scattoni, Giovanni Tonon, Antonio M. Persico
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Autism spectrum disorder (ASD) is a neurodevelopmental condition with onset in early childhood, still diagnosed only through clinical observation due to the lack of laboratory biomarkers. Early detection strategies would be especially useful
Externí odkaz:
https://doaj.org/article/145eb5975dc34ca795f6127c1f2c4542
Autor:
Francesca Cucinotta, Carla Lintas, Pasquale Tomaiuolo, Marco Baccarin, Chiara Picinelli, Paola Castronovo, Roberto Sacco, Ignazio Stefano Piras, Laura Turriziani, Arianna Ricciardello, Maria Luisa Scattoni, Antonio M. Persico
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 8, Pp n/a-n/a (2023)
Abstract Background Autism spectrum disorder (ASD) is characterized by high heritability estimates and recurrence rates; its genetic underpinnings are very heterogeneous and include variable combinations of common and rare variants. Array‐comparati
Externí odkaz:
https://doaj.org/article/0179a71ad8f24f04b221a0f378854198
Autor:
Antonio M. Persico
Publikováno v:
Frontiers in Psychiatry, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/67b0c677d5ce4f6a89cb6351b8ad59e3
Autor:
Pilar Garcés, Sarah Baumeister, Luke Mason, Christopher H. Chatham, Stefan Holiga, Juergen Dukart, Emily J. H. Jones, Tobias Banaschewski, Simon Baron-Cohen, Sven Bölte, Jan K. Buitelaar, Sarah Durston, Bob Oranje, Antonio M. Persico, Christian F. Beckmann, Thomas Bougeron, Flavio Dell’Acqua, Christine Ecker, Carolin Moessnang, Tony Charman, Julian Tillmann, Declan G. M. Murphy, Mark Johnson, Eva Loth, Daniel Brandeis, Joerg F. Hipp, The EU-AIMS LEAP group authorship
Publikováno v:
Molecular Autism, Vol 13, Iss 1, Pp 1-16 (2022)
Abstract Background Understanding the development of the neuronal circuitry underlying autism spectrum disorder (ASD) is critical to shed light into its etiology and for the development of treatment options. Resting state EEG provides a window into s
Externí odkaz:
https://doaj.org/article/eb81ea07e96244b0897ba1df29043f8e
Publikováno v:
Children, Vol 10, Iss 10, p 1653 (2023)
This study examines the last 10 years of medical literature on the benefits of cochlear implantation in children who are deaf or hard of hearing (DHH) with additional disabilities. The most recent literature concerning cochlear implants (CIs) in DHH
Externí odkaz:
https://doaj.org/article/a50225cb9afc442781359a5e18248bc5
Autor:
L. Mason, F. Shic, T. Falck-Ytter, B. Chakrabarti, T. Charman, E. Loth, J. Tillmann, T. Banaschewski, S. Baron-Cohen, S. Bölte, J. Buitelaar, S. Durston, B. Oranje, A. M. Persico, C. Beckmann, T. Bougeron, F. Dell’Acqua, C. Ecker, C. Moessnang, D. Murphy, M. H. Johnson, E. J. H. Jones, the LEAP Team
Publikováno v:
Molecular Autism, Vol 12, Iss 1, Pp 1-13 (2021)
Abstract Background The neurocognitive mechanisms underlying autism spectrum disorder (ASD) remain unclear. Progress has been largely hampered by small sample sizes, variable age ranges and resulting inconsistent findings. There is a pressing need fo
Externí odkaz:
https://doaj.org/article/ca8fcdcf48c74ee4a660f6b259d924ef
Autor:
Fethia Chehbani, Pasquale Tomaiuolo, Chiara Picinelli, Marco Baccarin, Paola Castronovo, Maria Luisa Scattoni, Naoufel Gaddour, Antonio M. Persico
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Background Autism spectrum disorder (ASD) is a neurodevelopmental disorder with strong genetic underpinnings. Microarray‐based comparative genomic hybridization (aCGH) technology has been proposed as a first‐level test in the genetic dia
Externí odkaz:
https://doaj.org/article/096cc6da0abe458cb193eb81c009335f