Publications in collaboration with researchers from Hospital Ramón y Cajal (14)

2023

  1. Hemihypomimia in Parkinson’s disease: an under-recognized clinical sign?

    Journal of Neurology

2022

  1. Stereoelectroencephalography in the preoperative assessment of patients with refractory focal epilepsy: Experience at an epilepsy centre

    Neurologia, Vol. 37, Núm. 5, pp. 334-345

2021

  1. Epilepsy Associated with Temporal Pole Encephaloceles: An Unrecognized Manifestation of Idiopathic Intracranial Hypertension?

    Clinical Neuroradiology, Vol. 31, Núm. 3, pp. 575-579

2020

  1. Diagnostic gap in genetic epilepsies: A matter of age

    Epilepsy and Behavior, Vol. 111

  2. Effectiveness and safety of perampanel monotherapy for focal and generalized tonic-clonic seizures: Experience from a national multicenter registry

    Epilepsia, Vol. 61, Núm. 6, pp. 1109-1119

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

    Epilepsia

  4. Impact of the Coronavirus Disease 2019 Pandemic on Functional Movement Disorders: Lessons From a Specialized Clinic

    Movement Disorders

2019

  1. Olfactory function in focal epilepsies: Understanding mesial temporal lobe epilepsy beyond the hippocampus

    Epilepsia Open, Vol. 4, Núm. 3, pp. 487-492

2018

  1. Paraneoplastic stiff person syndrome with small cell carcinoma of the bladder and anti-Ri antibodies

    Clinical Neurology and Neurosurgery, Vol. 173, pp. 194-195

2017

  1. Efficacy and safety of eslicarbazepine acetate monotherapy for partial-onset seizures: Experience from a multicenter, observational study

    Epilepsy and Behavior, Vol. 73, pp. 173-179

2016

  1. Small temporal pole encephalocele: A hidden cause of "normal" MRI temporal lobe epilepsy

    Epilepsia, Vol. 57, Núm. 5, pp. 841-851

2014

  1. Florbetapir (18F) for brain amyloid positron emission tomography: Highlights on the European marketing approval

    Alzheimer's and Dementia, Vol. 10, Núm. 5, pp. S395-S399

2010

  1. Clinical-genetic correlations in familial Alzheimer's disease caused by presenilin 1 mutations

    Journal of Alzheimer's Disease, Vol. 19, Núm. 3, pp. 873-884

1996

  1. Lipid composition of platelets in patients suffering from migraine without aura

    Headache, Vol. 36, Núm. 7, pp. 440-441