Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care
2018 · Genetics in Medicine · 106 citations
https://doi.org/10.1038/gim.2017.221
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Federico Raviglione
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Federico Raviglione is an academic researcher from Ospedale generale di zona San Camillo Treviso. The author has contributed to research in topics: Genetics and Neurodevelopmental Disorders & Congenital gastrointestinal and neural anomalies & Vascular anomalies and interventions. The author has an h-index of 11, co-authored 22 publications.
ORCID: 0000-0001-6799-2911Papers by this author
worksNeuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients
2016 · Genetics in Medicine · 55 citations
https://doi.org/10.1038/gim.2016.176
Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates
2021 · Clinical Neurophysiology · 49 citations
https://doi.org/10.1016/j.clinph.2021.01.012
Clinical findings in a patient with <i>FARS2</i> mutations and early‐infantile‐encephalopathy with epilepsy
2016 · American Journal of Medical Genetics Part A · 27 citations
https://doi.org/10.1002/ajmg.a.37836
Transitioning to adult mental health services for young people with ADHD: an Italian-based survey on practices for pediatric and adult services
2023 · Child and Adolescent Psychiatry and Mental Health · 4 citations
https://doi.org/10.1186/s13034-023-00678-9
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