Aglaia Vignoli

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 21

Top Venues

American journal of medical genetics. Part A

Healthcare (Basel, Switzerland)

Epileptic disorders : international epilepsy journal with videotape

Orphanet journal of rare diseases

University of Milan

University of Milan (PHD)

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

Affiliation History

University of Milan Dec 01 2012

Italy

Assistant Professor :: Department of Health Sciences

Azienda Ospedaliera San Paolo Sep 01 2004 - Nov 30 2012

Italy

Assistant Child Neurologist,

Azienda Ospedaliera Guido Salvini Dec 15 2000 - Aug 31 2004

Italy

Assistant Child Neurologist, :: Unit of Child Neurology and Psychiatry

Education History

University of Milan

Italy

PHD

Publications

Benedetta Cavirani, Carlotta Spagnoli, Stefano Giuseppe Caraffi, Anna Cavalli, Carlo Alberto Cesaroni, Gianni Cutillo, Valentina De Giorgis, Daniele Frattini, Giulia Bruna Marchetti, Silvia Masnada, Angela Peron, Susanna Rizzi, Costanza Varesio, Luigina Spaccini, Aglaia Vignoli, Maria Paola Canevini, Pierangelo Veggiotti, Livia Garavelli, Carlo Fusco
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study. International journal of molecular sciences 25 (2) (2024)
Anna Fetta, Francesco Toni, Ilaria Pettenuzzo, Emilia Ricci, Alessandro Rocca, Caterina Gambi, Luca Soliani, Veronica Di Pisa, Silvia Martini, Giacomo Sperti, Valeria Cagnazzo, Patrizia Accorsi, Emanuele Bartolini, Domenica Battaglia, Pia Bernardo, Maria Paola Canevini, Anna Rita Ferrari, Lucio Giordano, Chiara Locatelli, Margherita Mancardi, Alessandro Orsini, Tommaso Pippucci, Dario Pruna, Anna Rosati, Agnese Suppiej, Sara Tagliani, Alessandro Vaisfeld, Aglaia Vignoli, Kosuke Izumi, Ian Krantz, Duccio Maria Cordelli
Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children. Orphanet journal of rare diseases 19 (1) (2024)
Benedetta Cavirani, Carlotta Spagnoli, Stefano Giuseppe Caraffi, Anna Cavalli, Carlo Alberto Cesaroni, Gianni Cutillo, Valentina De Giorgis, Daniele Frattini, Giulia Bruna Marchetti, Silvia Masnada, Angela Peron, Susanna Rizzi, Costanza Varesio, Luigina Spaccini, Aglaia Vignoli, Maria Paola Canevini, Pierangelo Veggiotti, Livia Garavelli, Carlo Fusco
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study. International journal of molecular sciences 25 (2) (2024)
Anna Fetta, Francesco Toni, Ilaria Pettenuzzo, Emilia Ricci, Alessandro Rocca, Caterina Gambi, Luca Soliani, Veronica Di Pisa, Silvia Martini, Giacomo Sperti, Valeria Cagnazzo, Patrizia Accorsi, Emanuele Bartolini, Domenica Battaglia, Pia Bernardo, Maria Paola Canevini, Anna Rita Ferrari, Lucio Giordano, Chiara Locatelli, Margherita Mancardi, Alessandro Orsini, Tommaso Pippucci, Dario Pruna, Anna Rosati, Agnese Suppiej, Sara Tagliani, Alessandro Vaisfeld, Aglaia Vignoli, Kosuke Izumi, Ian Krantz, Duccio Maria Cordelli
Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children. Orphanet journal of rare diseases 19 (1) (2024)
Anna Fetta, Francesco Toni, Ilaria Pettenuzzo, Emilia Ricci, Alessandro Rocca, Caterina Gambi, Luca Soliani, Veronica Di Pisa, Silvia Martini, Giacomo Sperti, Valeria Cagnazzo, Patrizia Accorsi, Emanuele Bartolini, Domenica Battaglia, Pia Bernardo, Maria Paola Canevini, Anna Rita Ferrari, Lucio Giordano, Chiara Locatelli, Margherita Mancardi, Alessandro Orsini, Tommaso Pippucci, Dario Pruna, Anna Rosati, Agnese Suppiej, Sara Tagliani, Alessandro Vaisfeld, Aglaia Vignoli, Kosuke Izumi, Ian Krantz, Duccio Maria Cordelli
Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children. Orphanet journal of rare diseases 19 (1) (2024)
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)
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)
Katherine Turner, Francesca La Briola, Aglaia Vignoli, Elena Zambrelli, Valentina Chiesa, Laura Fongoni, Olivia Baldi, Maria Paola Canevini
Living with Epilepsy in Adolescence in Italy: Psychological and Behavioral Impact. Healthcare (Basel, Switzerland) 11 (5) (2023)
Katherine Turner, Francesca La Briola, Aglaia Vignoli, Elena Zambrelli, Valentina Chiesa, Laura Fongoni, Olivia Baldi, Maria Paola Canevini
Living with Epilepsy in Adolescence in Italy: Psychological and Behavioral Impact. Healthcare (Basel, Switzerland) 11 (5) (2023)
Katherine Turner, Francesca La Briola, Aglaia Vignoli, Elena Zambrelli, Valentina Chiesa, Laura Fongoni, Olivia Baldi, Maria Paola Canevini
Living with Epilepsy in Adolescence in Italy: Psychological and Behavioral Impact. Healthcare (Basel, Switzerland) 11 (5) (2023)
Sara Perego, Valentina Alari, Gianluca Pietra, Andrea Lamperti, Alessandro Vimercati, Nicole Camporeale, Maria Garzo, Francesca Cogliati, Donatella Milani, Aglaia Vignoli, Angela Peron, Lidia Larizza, Tommaso Pizzorusso, Silvia Russo
Modeling RTT Syndrome by iPSC-Derived Neurons from Male and Female Patients with Heterogeneously Severe Hot-Spot MECP2 Variants. International journal of molecular sciences 23 (22) (2022)
Hannah Stamberger, David Crosiers, Ganna Balagura, Claudia Maria Bonardi, Anna Basu, Gaetano Cantalupo, Valentina Chiesa, Jakob Christensen, Bernardo Dalla Bernardina, Colin A Ellis, Francesca Furia, Fiona Gardiner, Camille Giron, Renzo Guerrini, Karl Martin Klein, Christian Korff, Hana Krijtova, Melanie Leffler, Holger Lerche, Gaetan Lesca, David Lewis-Smith, Carla Marini, Dragan Marjanovic, Laure Mazzola, Sarah McKeown Ruggiero, Fanny Mochel, Francis Ramond, Philipp S Reif, Aurélie Richard-Mornas, Felix Rosenow, Christian Schropp, Rhys Huw Thomas, Aglaia Vignoli, Yvonne Weber, Emma Elizabeth Palmer, Ingo Helbig, Ingrid Eileen Scheffer, Pasquale Striano, Rikke Steensjerre Moller, Elena Gardella, Sarah Weckhuysen
Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood. Neurology 99 (3) (2022)
Elisabetta Di Fede, Angela Peron, Elisa Adele Colombo, Cristina Gervasini, Aglaia Vignoli
SLC35F1 as a candidate gene for neurodevelopmental disorders resembling Rett syndrome. American journal of medical genetics. Part A 185 (7) (2021)
Elena Zambrelli, Katherine Turner, Angela Peron, Alessia Leidi, Francesca La Briola, Aglaia Vignoli, Maria Paola Canevini
Sleep and behavior in children and adolescents with tuberous sclerosis complex. American journal of medical genetics. Part A 185 (5) (2021)
Angela Peron, Francesca La Briola, Fabio Bruschi, Silvia Terraneo, Chiara Vannicola, Roberto Previtali, Sabrina Perazzoli, Emanuela Morenghi, Gaetano Bulfamante, Aglaia Vignoli, Maria Paola Canevini
Tuberous sclerosis complex (TSC), lymphangioleiomyomatosis, and COVID-19: The experience of a TSC clinic in Italy. American journal of medical genetics. Part A 182 (11) (2020)
Angela Peron, Francesca Novara, Francesca La Briola, Elisabetta Merati, Emanuela Giannusa, Elena Segalini, Gloria Anniballi, Aglaia Vignoli, Roberto Ciccone, Maria Paola Canevini
Missense variants in the Arg206 residue of HNRNPH2: Further evidence of causality and expansion of the phenotype. American journal of medical genetics. Part A 182 (4) (2020)
Angela Peron, Maria Iascone, Elisabetta Salvatici, Benedetta Cavirani, Daniela Marchetti, Silvia Corno, Aglaia Vignoli
PIGW-related glycosylphosphatidylinositol deficiency: Description of a new patient and review of the literature. American journal of medical genetics. Part A 182 (6) (2020)
Lauren B Carter, Agatino Battaglia, Athena Cherry, Melanie A Manning, Maura Rz Ruzhnikov, Lynne M Bird, Leah Ke'ala'aumoe Dowsett, John M Graham, Fowzan Sami Alkuraya, Mais Hashem, Mary Beth Dinulos, Stephanie Vallee, Margaret P Adam, Ian Glass, Anita E Beck, Cathy A Stevens, Elaine Zackai, Carey McDougall, Beth Keena, Angela Peron, Aglaia Vignoli, Laurie H Seaver, Thomas P Slavin, Louanne Hudgins
Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy. American journal of medical genetics. Part A 179 (8) (2019)
Maria Paola Canevini, Katarzyna Kotulska-Jozwiak, Paolo Curatolo, Francesca La Briola, Angela Peron, Monika Słowińska, Jolanta Strzelecka, Aglaia Vignoli, Sergiusz Jóźwiak
Current concepts on epilepsy management in tuberous sclerosis complex. American journal of medical genetics. Part C, Seminars in medical genetics 178 (3) (2018)
Angela Peron, Maria Paola Canevini, Filippo Ghelma, Fabiano Di Marco, Aglaia Vignoli
Healthcare transition from childhood to adulthood in Tuberous Sclerosis Complex. American journal of medical genetics. Part C, Seminars in medical genetics 178 (3) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Aglaia Vignoli