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Author/Creator Raviglione, Federico

1. Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy. (21st March 2023)

Authors:
Carapancea, Evelina; Cornet, Marie-Coralie; Milh, Mathieu; De Cosmo, Lucrezia; Huang, Eric J.; Granata, Tiziana; Striano, Pasquale; Ceulemans, Berten; Stein, Anja; Morris-Rosendahl, Deborah; Conti, Greta; Mitra, Nipa; Raymond, F. Lucy; Rowitch, David H.; Solazzi, Roberta; Vercellino, Fabiana; De ...
Journal:
Neurology
Issue:
Volume 100:Number 12(2023)
Page Start:
e1234
Record Type:
Journal Article
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2. Clinical findings in a patient with FARS2 mutations and early‐infantile‐encephalopathy with epilepsy. Issue 11 (23rd August 2016)

Authors:
Raviglione, Federico; Conte, Giorgio; Ghezzi, Daniele; Parazzini, Cecilia; Righini, Andrea; Vergaro, Raffaella; Legati, Andrea; Spaccini, Luigina; Gasperini, Serena; Garavaglia, Barbara; Mastrangelo, Massimo
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 11(2016)
Page Start:
3004
Record Type:
Journal Article
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3. Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates. Issue 4 (April 2021)

Authors:
Dilena, Robertino; Raviglione, Federico; Cantalupo, Gaetano; Cordelli, Duccio M.; De Liso, Paola; Di Capua, Matteo; Falsaperla, Raffaele; Ferrari, Fabrizio; Fumagalli, Monica; Lori, Silvia; Suppiej, Agnese; Tadini, Laura; Dalla Bernardina, Bernardo; Mastrangelo, Massimo; Pisani, Francesco
Journal:
Clinical neurophysiology
Issue:
Volume 132:Issue 4(2021)
Page Start:
886
Record Type:
Journal Article
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4. Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European study. (May 2021)

Authors:
Raviglione, Federico; Douzgou, Sofia; Scala, Marcello; Mingarelli, Alessia; D'Arrigo, Stefano; Freri, Elena; Darra, Francesca; Giglio, Sabrina; Bonaglia, Maria C; Pantaleoni, Chiara; Mastrangelo, Massimo; Epifanio, Roberta; Elia, Maurizio; Saletti, Veronica; Morlino, Silvia; Vari, Maria Stella; D...
Journal:
Seizure
Issue:
Volume 88(2021)
Page Start:
60
Record Type:
Journal Article
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5. Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants. (December 2020)

Authors:
Malerba, Federica; Alberini, Giulio; Balagura, Ganna; Marchese, Francesca; Amadori, Elisabetta; Riva, Antonella; Vari, Maria Stella; Gennaro, Elena; Madia, Francesca; Salpietro, Vincenzo; Angriman, Marco; Giordano, Lucio; Accorsi, Patrizia; Trivisano, Marina; Specchio, Nicola; Russo, Angelo; Gobb...
Journal:
Neurology
Issue:
Volume 6:Number 6(2020)
Page Start:
Record Type:
Journal Article
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6. Seizures and EEG features in 74 patients with genetic‐dysmorphic syndromes. Issue 12 (24th September 2014)

Authors:
Alfei, Enrico; Raviglione, Federico; Franceschetti, Silvana; D'Arrigo, Stefano; Milani, Donatella; Selicorni, Angelo; Riva, Daria; Zuffardi, Orsetta; Pantaleoni, Chiara; Binelli, Simona
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 12(2014.)
Page Start:
3154
Record Type:
Journal Article
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