List of works - Lucio Giordano

Basal ganglia dysmorphism in patients with Aicardi syndrome

scientific article published on 04 December 2020

Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.

scientific article published on 22 March 2007

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

scientific article published on 19 November 2018

Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI.

scientific article

Early onset absence epilepsy with onset in the first year of life: a multicenter cohort study.

scientific article

Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndrome.

scientific article published on 27 August 2013

Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients.

scientific article

Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype

scientific article

Epilepsy in ring chromosome 20 syndrome

scientific article

Erratum to: Long-term outcome of epilepsy in patients with Prader–Willi syndrome

scientific article published on 01 January 2015

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients

scientific article

Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.

scientific article published on 29 January 2013

Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

scientific article published on 18 October 2014

Neuroimaging Changes in Menkes Disease, Part 2.

scientific article

Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?

scientific article

Refractory absence seizures: An Italian multicenter retrospective study.

scientific article published on 18 July 2015

SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.

scientific article published on 12 March 2009

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

scientific article published on 20 October 2016

The spectrum of intermediate SCN8A-related epilepsy

scientific article published on 10 April 2019

List of works by Lucio Giordano

Basal ganglia dysmorphism in patients with Aicardi syndrome

Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.

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

Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI.

Early onset absence epilepsy with onset in the first year of life: a multicenter cohort study.

Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndrome.

Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients.

Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype

Epilepsy in ring chromosome 20 syndrome

Erratum to: Long-term outcome of epilepsy in patients with Prader–Willi syndrome

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients

Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.

Long-term outcome of epilepsy in patients with Prader-Willi syndrome.

Neuroimaging Changes in Menkes Disease, Part 2.

Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?

Refractory absence seizures: An Italian multicenter retrospective study.

SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.

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

The spectrum of intermediate SCN8A-related epilepsy