Lia Santulli

Via Pansini 5
Naples, 80131, Italy

Last Updated: 09/26/2026

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Found 12 publications

Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases.

Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases.

Journal: Seizure

Published: July 26, 2018

The challenges of treating epilepsy with 25 antiepileptic drugs.

The challenges of treating epilepsy with 25 antiepileptic drugs.

Journal: Pharmacological research

Published: February 09, 2016

Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy.

Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy.

Journal: Epilepsy & behavior : E&B

Published: October 20, 2015

17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome.

17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome.

Journal: Brain & development

Published: September 06, 2015

DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy.

DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy.

Journal: Epilepsia

Published: June 30, 2015

Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras.

Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras.

Journal: Epilepsy research

Published: August 12, 2014

Neurological features and long-term follow-up in 15q11.2-13.1 duplication.

Neurological features and long-term follow-up in 15q11.2-13.1 duplication.

Journal: European journal of medical genetics

Published: June 18, 2013

Spontaneous intracranial hypotension and epidural blood patch: a report involving seven cases.

Spontaneous intracranial hypotension and epidural blood patch: a report involving seven cases.

Journal: Anaesthesia and intensive care

Published: May 11, 2013

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

Journal: Epilepsia

Published: March 12, 2013

Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion.

Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion.

Journal: Epilepsia

Published: January 20, 2013

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.

Journal: Neurology

Published: April 13, 2012

The gelastic seizures-hypothalamic hamartoma syndrome: facts, hypotheses, and perspectives.

The gelastic seizures-hypothalamic hamartoma syndrome: facts, hypotheses, and perspectives.

Journal: Epilepsy & behavior : E&B

Published: January 10, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026