Rosaria Vavassori
Palermo, Italy
Last Updated: 09/26/2026
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Found 14 publications
Natural History of Alternating Hemiplegia of Childhood: Vulnerabilities in Early Childhood and Predictive Factors for Long-Term Outcomes.
Journal: Annals of the Child Neurology Society
Published: June 14, 2025
ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular Arrhythmias.
Journal: JAMA pediatrics
Published: March 03, 2025
Characterization of Sleep in Alternating Hemiplegia of Childhood: An International Survey.
Journal: Neurology. Genetics
Published: February 10, 2025
Children and Adolescent Patients with Variants in the ATP1A3 -encoded Sodium-Potassium ATPase Alpha-3 Subunit Demonstrate an Impaired QT Response to Bradycardia and Predisposition to Sinus Node Dysfunction.
Journal: medRxiv : the preprint server for health sciences
Published: September 10, 2024
Methodology of a Natural History Study of a Rare Neurodevelopmental Disorder: Alternating Hemiplegia of Childhood as a Prototype Disease.
Journal: Journal of child neurology
Published: September 20, 2023
Real life retrospective study of cannabidiol therapy in alternating hemiplegia of childhood.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: August 10, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene.
Journal: European journal of human genetics : EJHG
Published: August 01, 2023
Development and testing of methods to record and follow up spells in patients with alternating hemiplegia of childhood.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: February 28, 2023
Rare. The importance of research, analysis, reporting and education in 'solving' the genetic epilepsies: A perspective from the European patient advocacy group for EpiCARE.
Journal: European journal of medical genetics
Published: April 26, 2021
Alternating hemiplegia of childhood: evolution over time and mouse model corroboration.
Journal: Brain communications
Published: March 05, 2021
Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study.
Journal: Neurology
Published: December 23, 2019
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
Journal: Orphanet journal of rare diseases
Published: March 11, 2015
Last Updated: 09/26/2026