List of works - Ilaria Contaldo

A prospective longitudinal study on visuo-cognitive development in Dravet syndrome: Is there a "dorsal stream vulnerability"?

scientific article published on 28 October 2014

Acneiform eruption induced by ethosuximide

scientific article published on 01 January 2014

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

scientific article published on 15 February 2017

Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutation.

scientific article published on 30 July 2014

Cognitive decline in Dravet syndrome: is there a cerebellar role?

scientific article published on 30 April 2013

Cognitive-behavioral profiles in teenagers with Dravet syndrome.

scientific article published on 18 January 2016

Early visual assessment in preterm infants with and without brain lesions: correlation with visual and neurodevelopmental outcome at 12 months

scientific article published on 14 January 2011

Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients

scientific article published on 30 September 2015

Longstanding epileptic encephalopathy and linear localized scleroderma: two distinct pathologic processes in an adolescent

scientific article published on 16 February 2008

Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome.

scientific article

Seizure semiology of lesional frontal lobe epilepsies in children.

scientific article published in December 2007

Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases).

scientific article published on 28 October 2014

Surgery for posterior quadrantic cortical dysplasia. A review

scientific article

Surgery of children with frontal lobe lesional epilepsy: neuropsychological study.

scientific article published on 5 November 2010

Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples.

scientific article

The forward parachute reaction and independent walking in infants with brain lesions

scientific article published on 21 March 2011

Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.

scientific article published on 16 April 2014

List of works by Ilaria Contaldo

A prospective longitudinal study on visuo-cognitive development in Dravet syndrome: Is there a "dorsal stream vulnerability"?

Acneiform eruption induced by ethosuximide

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

Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutation.

Cognitive decline in Dravet syndrome: is there a cerebellar role?

Cognitive-behavioral profiles in teenagers with Dravet syndrome.

Early visual assessment in preterm infants with and without brain lesions: correlation with visual and neurodevelopmental outcome at 12 months

Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients

Longstanding epileptic encephalopathy and linear localized scleroderma: two distinct pathologic processes in an adolescent

Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome.

Seizure semiology of lesional frontal lobe epilepsies in children.

Sleep-potentiated epileptiform activity in early thalamic injuries: Study in a large series (60 cases).

Surgery for posterior quadrantic cortical dysplasia. A review

Surgery of children with frontal lobe lesional epilepsy: neuropsychological study.

Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples.

The forward parachute reaction and independent walking in infants with brain lesions

Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.