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List of works by Domenica Battaglia

Chromosome 9p deletion syndrome and sex reversal: Novel findings and redefinition of the critically deleted regions ⬇️

scientific article published on July 20, 2012

Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations

scientific article published on 15 February 2017

Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients

scientific article published in January 2011

Corrigendum to "Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study" [Epilepsy Behav. Oct 2017; 75C:151-157].

scientific article published in March 2018

Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study

scientific article published on 19 November 2018

Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy.

scientific article

Early development in Dravet syndrome; visual function impairment precedes cognitive decline ⬇️

scientific article published on November 24, 2010

Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study

scientific article published on 18 September 2020

Electrical and autonomic cardiac function in patients with Dravet syndrome ⬇️

scientific article published on April 1, 2011

Family study of epilepsy in first degree relatives: data from the Italian Episcreen Study

scientific article published in June 2003

Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy

scientific article

Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes

scientific article published in 2022

Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study.

scientific article published on 31 August 2017

Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype ⬇️

scientific article published on April 29, 2012

Neuropsychological development in children with Dravet syndrome ⬇️

scientific article published on April 6, 2011

PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine.

scientific article

Posterior resection for childhood lesional epilepsy: Neuropsychological evolution ⬇️

scientific article published on January 5, 2012

Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre study

scientific article published on 20 October 2016

Temporal lobe epilepsy surgery in children and adults: A multicenter study

scientific article published on 01 December 2020

Trends in pediatric epilepsy surgery in Europe between 2008 and 2015: Country-, center-, and age-specific variation

scientific article published on 26 December 2019

Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16

scientific article published on 04 August 2007

Wolf–Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16

scientific article published on 15 February 2008

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