Participación en Proyectos de Investigación

2020

Adverse effects of cannabinoids.

Epileptic Disord. 2020 Jan 1;22(S1):29-32. doi: 10.1684/epd.2019.1125.

2020

Antiseizure medication withdrawal in seizure-free patients with PCDH19-related epilepsy: A multinational cohort survey.

Seizure. 2020 Jun 5;80:259-261. doi: 10.1016/j.seizure.2020.06.007. Online ahead of print.
PMID: 32682289

2020

Analysis of the family impact and needs of Dravet's syndrome in Spain.

Rev Neurol. 2020 Feb 1;70(3):75-83. doi: 10.33588/rn.7003.2019310.

2020

Diagnostic gap in genetic epilepsies: A matter of age.

Epilepsy Behav. 2020 Jun 28;111:107266. doi: 10.1016/j.yebeh.2020.107266. Online ahead of print.
PMID: 32610249

2020

Genetic epilepsies and COVID-19 pandemic: Lessons from the caregiver perspective.

Epilepsia. 2020. un;61(6):1312-1314. doi: 10.1111/epi.16537. Epub 2020 May 18.
PMID: 32420620

2019

Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical Trial.

JAMA Neurol. 2019 Dec 2;77(3):300-308. doi: 10.1001/jamaneurol.2019.4113. Online ahead of print.

2019

Ascertaining the epidemiology, patient flow and disease management for Dravet syndrome in Spain.

Rev Neurol. 2019 Jan 16;68(2):75-81.

2019

Patients' knowledge on epilepsy and SUDEP improves after a semi-structured health interview.

Epilepsy Behav. 2019 Oct;99:106467. doi: 10.1016/j.yebeh.2019.106467. Epub 2019 Aug 14.

2018

Genetic (idiopathic) generalized epilepsy with occipital semiology.

Epileptic Disord. 2018 Oct 1;20(5):434-439. doi: 10.1684/epd.2018.0994.

2018

Specificity of electroclinical features in the diagnosis of ring chromosome 20.

Epilepsy Behav. 2018 Mar;80:215-220. doi: 10.1016/j.yebeh.2017.12.001. Epub 2018 Feb 3.

2017

Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico-Pathological Entity.

Brain Pathol. 2017 Jan;27(1):26-35. doi: 10.1111/bpa.12347. Epub 2016 Feb 22.