Federico Raviglione

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 10

Top Topics

Low Birth Weight

Preterm Infants

Epithelial Mesenchymal Transition

Top Venues

Epileptic disorders : international epilepsy journal with videotape

Case reports in genetics

Genetics in medicine : official journal of the American College of Medical Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Martina Paola Zanaboni, Ludovica Pasca, Stefania Maria Bova, Matteo Alessio Chiappedi, Melissa Filippini, Lucio Giordano, Serena Grumi, Serena Micheletti, Francesca Felicia Operto, Dario Pruna, Francesca Ragona, Federico Raviglione, Martina Totaro, Costanza Varesio, Aglaia Vignoli, Valentina De Giorgis, null null
WISC-IV intellectual profiles in Italian children with self-limited epilepsy with centrotemporal spikes. Epileptic disorders : international epilepsy journal with videotape 25 (2) (2023)
Martina Paola Zanaboni, Ludovica Pasca, Stefania Maria Bova, Matteo Alessio Chiappedi, Melissa Filippini, Lucio Giordano, Serena Grumi, Serena Micheletti, Francesca Felicia Operto, Dario Pruna, Francesca Ragona, Federico Raviglione, Martina Totaro, Costanza Varesio, Aglaia Vignoli, Valentina De Giorgis, null null
WISC-IV intellectual profiles in Italian children with self-limited epilepsy with centrotemporal spikes. Epileptic disorders : international epilepsy journal with videotape 25 (2) (2023)
Evelina Carapancea, Marie-Coralie Cornet, Mathieu Milh, Lucrezia De Cosmo, Eric J Huang, Tiziana Granata, Pasquale Striano, Berten Ceulemans, Anja Stein, Deborah J Morris-Rosendahl, Greta Conti, Nipa Mitra, F Lucy Raymond, David H Rowitch, Roberta Solazzi, Fabiana Vercellino, Paola De Liso, Gianluca D'Onofrio, Clementina Boniver, Olivier Danhaive, Katherine Carkeek, Vincenzo Salpietro, Sarah Weckhuysen, Marny Fedrigo, Annalisa Angelini, Barbara Castellotti, Damien Lederer, Valérie Benoit, Federico Raviglione, Renzo Guerrini, Robertino Dilena, Maria Roberta Cilio
Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy. Neurology 100 (12) (2023)
Evelina Carapancea, Marie-Coralie Cornet, Mathieu Milh, Lucrezia De Cosmo, Eric J Huang, Tiziana Granata, Pasquale Striano, Berten Ceulemans, Anja Stein, Deborah J Morris-Rosendahl, Greta Conti, Nipa Mitra, F Lucy Raymond, David H Rowitch, Roberta Solazzi, Fabiana Vercellino, Paola De Liso, Gianluca D'Onofrio, Clementina Boniver, Olivier Danhaive, Katherine Carkeek, Vincenzo Salpietro, Sarah Weckhuysen, Marny Fedrigo, Annalisa Angelini, Barbara Castellotti, Damien Lederer, Valérie Benoit, Federico Raviglione, Renzo Guerrini, Robertino Dilena, Maria Roberta Cilio
Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy. Neurology 100 (12) (2023)
Martina Paola Zanaboni, Ludovica Pasca, Stefania Maria Bova, Matteo Alessio Chiappedi, Melissa Filippini, Lucio Giordano, Serena Grumi, Serena Micheletti, Francesca Felicia Operto, Dario Pruna, Francesca Ragona, Federico Raviglione, Martina Totaro, Costanza Varesio, Aglaia Vignoli, Valentina De Giorgis, null null
WISC-IV intellectual profiles in Italian children with self-limited epilepsy with centrotemporal spikes. Epileptic disorders : international epilepsy journal with videotape 25 (2) (2023)
Alessia Mingarelli, Giovanni Battista Pipitone, Giacomo Torini, Maria Grazia Patricelli, Martina Totaro, Clara Colonna, Paola Carrera, Federico Raviglione
Behavioral Phenotype, Electroclinical Features, and Treatment Options in Twins with Lrp2 Candidate Variants (Donnay-Barrow/Foar Syndrome). Case reports in genetics 2023 (2023)
Evelina Carapancea, Marie-Coralie Cornet, Mathieu Milh, Lucrezia De Cosmo, Eric J Huang, Tiziana Granata, Pasquale Striano, Berten Ceulemans, Anja Stein, Deborah J Morris-Rosendahl, Greta Conti, Nipa Mitra, F Lucy Raymond, David H Rowitch, Roberta Solazzi, Fabiana Vercellino, Paola De Liso, Gianluca D'Onofrio, Clementina Boniver, Olivier Danhaive, Katherine Carkeek, Vincenzo Salpietro, Sarah Weckhuysen, Marny Fedrigo, Annalisa Angelini, Barbara Castellotti, Damien Lederer, Valérie Benoit, Federico Raviglione, Renzo Guerrini, Robertino Dilena, Maria Roberta Cilio
Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy. Neurology 100 (12) (2023)
Evelina Carapancea, Marie-Coralie Cornet, Mathieu Milh, Lucrezia De Cosmo, Eric J Huang, Tiziana Granata, Pasquale Striano, Berten Ceulemans, Anja Stein, Deborah J Morris-Rosendahl, Greta Conti, Nipa Mitra, F Lucy Raymond, David H Rowitch, Roberta Solazzi, Fabiana Vercellino, Paola De Liso, Gianluca D'Onofrio, Clementina Boniver, Olivier Danhaive, Katherine Carkeek, Vincenzo Salpietro, Sarah Weckhuysen, Marny Fedrigo, Annalisa Angelini, Barbara Castellotti, Damien Lederer, Valérie Benoit, Federico Raviglione, Renzo Guerrini, Robertino Dilena, Maria Roberta Cilio
Clinical and Neurophysiologic Phenotypes in Neonates With BRAT1 Encephalopathy. Neurology 100 (12) (2023)
Federica Malerba, Giulio Alberini, Ganna Balagura, Francesca Marchese, Elisabetta Amadori, Antonella Riva, Maria Stella Vari, Elena Gennaro, Francesca Madia, Vincenzo Salpietro, Marco Angriman, Lucio Giordano, Patrizia Accorsi, Marina Trivisano, Nicola Specchio, Angelo Russo, Giuseppe Gobbi, Federico Raviglione, Tiziana Pisano, Carla Marini, Maria M Mancardi, Lino Nobili, Elena Freri, Barbara Castellotti, Giuseppe Capovilla, Antonietta Coppola, Alberto Verrotti, Paola Martelli, Francesco Miceli, Luca Maragliano, Fabio Benfenati, Maria R Cilio, Katrine Marie Johannesen, Rikke Steensjerre Moller, Berten Ceulemans, Carlo Minetti, Sarah Weckhuysen, Federico Zara, Maurizio Taglialatela, Pasquale Striano
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants. Neurology. Genetics 6 (6) (2020)
Livia Garavelli, Ivan Ivanovski, Stefano Giuseppe Caraffi, Daniela Santodirocco, Marzia Pollazzon, Duccio Maria Cordelli, Ebtesam Abdalla, Patrizia Accorsi, Margaret P Adam, Chiara Baldo, Allan Bayat, Elga Belligni, Federico Bonvicini, Jeroen Breckpot, Bert Callewaert, Guido Cocchi, Goran Cuturilo, Koenraad Devriendt, Mary Beth Dinulos, Olivera Djuric, Roberta Epifanio, Francesca Faravelli, Debora Formisano, Lucio Giordano, Marina Grasso, Sabine Grønborg, Alessandro Iodice, Lorenzo Lughetti, Didier Lacombe, Massimo Maggi, Baris Malbora, Isabella Mammi, Sebastien Moutton, Rikke Møller, Petra Muschke, Manuela Napoli, Chiara Pantaleoni, Rosario Pascarella, Alessandro Pellicciari, Maria Luisa Poch-Olive, Federico Raviglione, Francesca Rivieri, Carmela Russo, Salvatore Savasta, Gioacchino Scarano, Angelo Selicorni, Margherita Silengo, Giovanni Sorge, Luigi Tarani, Luis Gonzaga Tone, Annick Toutain, Aurélien Trimouille, Elvis Terci Valera, Samantha A Schrier Vergano, Nicoletta Zanotta, Marcella Zollino, William B Dobyns, Alex R Paciorkowski
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients. Genetics in medicine : official journal of the American College of Medical Genetics 19 (6) (2016)