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Aglaia Vignoli

Showing results (91-100 of 129) with videos related to

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Frontiers in Neurology|January 3, 2022
Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic StudyAnna Fetta, Veronica Di Pisa, Martina Ruscelli, et al.
Genes|March 25, 2022
<i>KMT2A</i>: Umbrella Gene for Multiple DiseasesSilvia Castiglioni, Elisabetta Di Fede, Clara Bernardelli, et al.
Epilepsy & Behavior : E&B|October 18, 2025
Developmental and epileptic encephalopathies: From current care to future perspectives - insights from epilepsy centres in Lombardy, ItalyGiuseppe Didato, Francesca Ragona, Alice Pompili, et al.
BMJ Open|June 3, 2026
Microbiota-gut-brain axis and treatment resistance in epilepsy: a multicentre prospective study protocol (CARE)Elisa Borghi, Laura Tassi, Giuseppe d'Orsi, et al.
Epilepsy & Behavior : E&B|February 15, 2026
Behind the seizures: Exploring the emotional burden of adolescents with idiopathic generalized epilepsyMartina Paola Zanaboni, Alessandra Raspanti, Carlo Alberto Quaranta, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 26, 2023
WISC-IV intellectual profiles in Italian children with self-limited epilepsy with centrotemporal spikesMartina Paola Zanaboni, Ludovica Pasca, Stefania Maria Bova, et al.
Epilepsia Open|February 9, 2024
Myoclonus: Differential diagnosis and current managementAntonella Riva, Gianluca D'Onofrio, Edoardo Ferlazzo, et al.
Epilepsia|May 15, 2012
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literatureAglaia Vignoli, Renato Borgatti, Angela Peron, et al.
Epilepsy Research|November 7, 2016
Epilepsy in ring chromosome 20 syndromeAglaia Vignoli, Francesca Bisulli, Francesca Darra, et al.
International Journal of Molecular Sciences|July 27, 2019
Pathogenic Variants in <i>STXBP1</i> and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like PhenotypesFrancesca Cogliati, Valentina Giorgini, Maura Masciadri, et al.
Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:
Pageof 13
Frontiers in Neurology|January 3, 2022
Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic StudyAnna Fetta, Veronica Di Pisa, Martina Ruscelli, et al.
Genes|March 25, 2022
<i>KMT2A</i>: Umbrella Gene for Multiple DiseasesSilvia Castiglioni, Elisabetta Di Fede, Clara Bernardelli, et al.
Epilepsy & Behavior : E&B|October 18, 2025
Developmental and epileptic encephalopathies: From current care to future perspectives - insights from epilepsy centres in Lombardy, ItalyGiuseppe Didato, Francesca Ragona, Alice Pompili, et al.
BMJ Open|June 3, 2026
Microbiota-gut-brain axis and treatment resistance in epilepsy: a multicentre prospective study protocol (CARE)Elisa Borghi, Laura Tassi, Giuseppe d'Orsi, et al.
Epilepsy & Behavior : E&B|February 15, 2026
Behind the seizures: Exploring the emotional burden of adolescents with idiopathic generalized epilepsyMartina Paola Zanaboni, Alessandra Raspanti, Carlo Alberto Quaranta, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 26, 2023
WISC-IV intellectual profiles in Italian children with self-limited epilepsy with centrotemporal spikesMartina Paola Zanaboni, Ludovica Pasca, Stefania Maria Bova, et al.
Epilepsia Open|February 9, 2024
Myoclonus: Differential diagnosis and current managementAntonella Riva, Gianluca D'Onofrio, Edoardo Ferlazzo, et al.
Epilepsia|May 15, 2012
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literatureAglaia Vignoli, Renato Borgatti, Angela Peron, et al.
Epilepsy Research|November 7, 2016
Epilepsy in ring chromosome 20 syndromeAglaia Vignoli, Francesca Bisulli, Francesca Darra, et al.
International Journal of Molecular Sciences|July 27, 2019
Pathogenic Variants in <i>STXBP1</i> and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like PhenotypesFrancesca Cogliati, Valentina Giorgini, Maura Masciadri, et al.
Pageof 13