Publications by authors named "Roberta Solazzi"

Claim this Profile
C
Compound Heterozygous Variants Causing Developmental and Epileptic Encephalopathy with Severe Microcephaly: Natural History of Two New Cases and Literature Review.
Francesca Ragona, Giuliana Messina, Stefania Magri, Fabio Martino Doniselli, Elena Freri, Roberta Solazzi

NeuroSci· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic complexity in pediatric onset epilepsy-movement disorder syndromes: Insights from a cohort of 97 subjects.
Davide Caputo, Roberta Solazzi, Barbara Castellotti, Celeste Panteghini, Francesca Luisa Sciacca

Epilepsia· October 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiology.
Simona Balestrini, Ilaria Galli, Maria Luisa Ricci, Elena Parrini, Davide Mei, Roberta Solazzi

Epilepsia· October 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CLN6-related continuum phenotype caused by aberrant splicing.
Federica Invernizzi, Barbara Castellotti, Chiara Reale, Celeste Panteghini, Isabel Colangelo, Roberta Solazzi

Epilepsia Open· February 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pharmacological approaches in drug-resistant pediatric epilepsies caused by pathogenic variants in potassium channel genes.
Ilaria Filareto, Ilaria Mosca, Elena Freri, Francesca Ragona, Laura Canafoglia, Roberta Solazzi

Front Cell Neurosci· January 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Next-generation sequencing in pediatric-onset epilepsies: Analysis with target panels and personalized therapeutic approach.
Barbara Castellotti, Francesca Ragona, Elena Freri, Giuliana Messina, Stefania Magri, Roberta Solazzi

Epilepsia Open· October 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cortical Myoclonus and Complex Paroxysmal Dyskinesias in a Patient with NAA15 Variant.
Elena Freri, Laura Canafoglia, Claudia Ciaccio, Davide Rossi Sebastiano, Davide Caputo, Roberta Solazzi

Mov Disord· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and molecular characterization of patients with YWHAG-related epilepsy.
Valentina Cetica, Tiziana Pisano, Gaetan Lesca, Dana Marafi, Laura Licchetta, Roberta Solazzi

Epilepsia· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with -related drug-resistant focal epilepsy.
Ilaria Mosca, Elena Freri, Paolo Ambrosino, Giorgio Belperio, Tiziana Granata, Roberta Solazzi

Front Cell Neurosci· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet.
Jacopo C DiFrancesco, Francesca Ragona, Carmen Murano, Anthony Frosio, Dario Melgari, Roberta Solazzi

Epilepsia· December 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Repetitive Sleep Starts in Allan-Herndon-Dudley Syndrome.
Roberta Solazzi, Giuliana Nanni, Silvia Esposito, Margherita Estienne, Elena Freri

Pediatr Neurol· October 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndrome.
Nicola Specchio, Marina Trivisano, Matteo Lenge, Alessandro Ferretti, Davide Mei, Roberta Solazzi

Cereb Cortex· August 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine.
Paolo Ambrosino, Francesca Ragona, Ilaria Mosca, Chiara Vannicola, Laura Canafoglia, Roberta Solazzi

Epilepsia· July 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Gelastic seizures and "smiling spasms": A peculiar ictal pattern.
Tommaso Lo Barco, Laura Corona, Roberta Solazzi, Elena Fiorini, Giulia Galati

Epileptic Disord· April 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and Neurophysiologic Phenotypes in Neonates With Encephalopathy.
Evelina Carapancea, Marie-Coralie Cornet, Mathieu Milh, Lucrezia De Cosmo, Eric J Huang, Roberta Solazzi

Neurology· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Severe Epilepsy and Movement Disorder May Be Early Symptoms of -Related Hypomyelinating Leukodystrophy.
Roberta Solazzi, Marco Moscatelli, Davide Rossi Sebastiano, Laura Canafoglia, Laura Pezzoli

Neurol Genet· October 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Early-onset bradykinetic rigid syndrome and reflex seizures in a child with PURA syndrome.
Roberta Solazzi, Elena Fiorini, Elena Parrini, Renzo Guerrini, Bernardo Dalla Bernardina

Epileptic Disord· October 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Paroxysmal tonic upgaze in a child with SCN8A-related encephalopathy.
Roberta Solazzi, Barbara Castellotti, Laura Canafoglia, Giuliana Messina, Stefania Magri

Epileptic Disord· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CDKL5 deficiency disorder in males: Five new variants and review of the literature.
Barbara Siri, Costanza Varesio, Elena Freri, Francesca Darra, Simone Gana, Roberta Solazzi

Eur J Paediatr Neurol· July 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Severe epilepsy in CNTNAP2-related Pitt-Hopkins-like syndrome successfully treated with stiripentol.
Elena Freri, Barbara Castellotti, Laura Canafoglia, Francesca Ragona, Roberta Solazzi

Seizure· May 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Letter to the Editor Regarding the Article "Whole-Exome Sequencing in NF1-Related West's Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy".
Luigi Vetri, Francesco Calì, Mirella Vinci, Carmelo Amato, Michele Roccella, Roberta Solazzi

Neuropediatrics· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SYNGAP1-DEE: A visual sensitive epilepsy.
Tommaso Lo Barco, Anna Kaminska, Roberta Solazzi, Claude Cancés, Giulia Barcia

Clin Neurophysiol· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome.
Silvia Masnada, Anna Pichiecchio, Manuela Formica, Filippo Arrigoni, Paola Borrelli, Roberta Solazzi

Neurology· March 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SCN8A splicing mutation causing skipping of the exon 15 associated with intellectual disability and cortical myoclonus.
Laura Canafoglia, Silvana Franceschetti, Tiziana Granata, Giuliana Messina, Roberta Solazzi

Seizure· November 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy.
Maria Virginia Soldovieri, Elena Freri, Paolo Ambrosino, Ilaria Rivolta, Ilaria Mosca, Roberta Solazzi

Pharmacol Res· October 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis