RAVIGLIONE, FEDERICO

RAVIGLIONE, FEDERICO  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Correspondence on “Expanded phenotype of AARS1-related white matter disease” by Helman et al 2022 Leidi A.Previtali R.Raviglione F.Carelli S.Tonduti D. + Article (author) -
Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individuals 2021 Ricci, EmiliaFinardi, EricaRaviglione, FedericoVignoli, AglaiaCanevini, Mariapaola + Article (author) -
Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates 2021 Dilena R.Raviglione F.Di Capua M.Fumagalli M.Pisani F. + Article (author) -
Mowat-Wilson syndrome : growth charts 2020 Otelli V.Raviglione F.Ricci E. + Article (author) -
Sleep in Mowat-Wilson Syndrome : a clinical and video-polysomnographic study 2019 Ricci E.Raviglione F. + Article (author) -
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care 2018 Raviglione F.Ricci E. + Article (author) -
Neonatal suppression-burst without epileptic seizures : Expanding the electroclinical phenotype of STXBP1-related, early-onset encephalopathy 2013 A. PeronRAVIGLIONE, FEDERICO + Article (author) -
Neuropsychological findings and psychiatric comorbitities in childhood idiopathic generalized epilepsies 2011 M. SaviniA. VignoliK. TurnerF. RaviglioneF. La BriolaM.P. CaneviniC. Lenti + Article (author) -