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Long‐term safety and efficacy of add‐on cannabidiol in patients with Lennox–Gastaut syndrome: Results of a long‐term open‐label extension trial

Epilepsia (Copenhagen), 2021-09, Vol.62 (9), p.2228-2239

2021

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Temporal pole epilepsy: Do not forget to look for occult encephaloceles

Epilepsia (Copenhagen), 2020-12, Vol.61 (12), p.2859-2860

2020

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Fenfluramine significantly reduces day‐to‐day seizure burden by increasing number of seizure‐free days and time between seizures in patients with Dravet syndrome: A time‐to‐event analysis

Epilepsia (Copenhagen), 2022-01, Vol.63 (1), p.130-138

2022

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

Epilepsia (Copenhagen), 2020-06, Vol.61 (6), p.1312-1314

2020

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Epilepsy and cannabidiol: a guide to treatment

Epileptic disorders, 2020-02, Vol.22 (1), p.1-14

2020

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Adverse effects of cannabinoids

Epileptic disorders, 2020-01, Vol.22 (S1), p.S29-S32

2020

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Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox–Gastaut syndrome: Interim analysis of an open‐label extension study

Epilepsia (Copenhagen), 2023-01, Vol.64 (1), p.139-151

2023

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Comprehensive scoping review of fenfluramine's role in managing generalized tonic–clonic seizures in developmental and epileptic encephalopathies

Epilepsia (Copenhagen), 2024-08, Vol.65 (8), p.2186-2199

2024

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Long‐term evaluation of anterior thalamic deep brain stimulation for epilepsy in the European MORE registry

Epilepsia (Copenhagen), 2024-08, Vol.65 (8), p.2438-2458

2024

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The burden of epilepsy and unmet need in people with focal seizures

Brain and behavior, 2022-09, Vol.12 (9), p.e2589-n/a

2022

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GPI‐anchoring disorders and the heart: Is cardiomyopathy an overlooked feature?

Clinical genetics, 2023-11, Vol.104 (5), p.598-603

2023

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Epileptogenic focal lesions in Dravet syndrome: A warning to investigators

Epileptic disorders, 2024-04, Vol.26 (2), p.173-180

2024

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Anterior midcingulate epilepsy: When semiology is of paramount importance to find the needle in the haystack

Epileptic disorders, 2024-02, Vol.26 (1), p.161-163

2024

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An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real‐world practice setting: A report from the Fenfluramine European Early Access Program

Epilepsia open, 2022-12, Vol.7 (4), p.578-587

2022

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Hippocampal sclerosis caused by repetitive parieto‐insular seizures through a possible kindling mechanism

Epileptic disorders, 2022-06, Vol.24 (3), p.621-622

2022

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Spanish consensus on the management of concomitant antiseizure medications when using cenobamate in adults with drug‐resistant focal seizures

Epilepsia open, 2024-06, Vol.9 (3), p.1051-1058

2024

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Consensus statement for the management of generalized tonic‐clonic seizures in Spain

Acta neurologica Scandinavica, 2020-01, Vol.141 (1), p.22-32

2020

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Corticospinal tract displacement due to a large malformation during cortical development

Epileptic disorders, 2020-10, Vol.22 (5), p.695-696

2020

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Efficacy and tolerability of add-on stiripentol in real-world clinical practice: An observational study in Dravet syndrome and non-Dravet developmental and epileptic encephalopathies

Epilepsia open, 2024-02, Vol.9 (1), p.164-175

2024

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Effect of fenfluramine on seizures and comorbidities in SCN8A‐developmental and epileptic encephalopathy: A case series

Epilepsia open, 2022-09, Vol.7 (3), p.525-531

2022

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Patient profile, management, and quality of life associated with Dravet syndrome: a cross-sectional, multicentre study of 80 patients in Spain

Scientific reports, 2023-02, Vol.13 (1), p.3355-3355, Article 3355

2023

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Genetic (idiopathic) generalized epilepsy with occipital semiology

Epileptic disorders, 2018-10, Vol.20 (5), p.434-439

2018

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

Epilepsia open, 2019-09, Vol.4 (3), p.487-492

2019

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Testing patients during seizures: A European consensus procedure developed by a joint taskforce of the ILAE – Commission on European Affairs and the European Epilepsy Monitoring Unit Association

Epilepsia (Copenhagen), 2016-09, Vol.57 (9), p.1363-1368

2016

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Long‐term safety and efficacy of add‐on cannabidiol in patients with Lennox–Gastaut syndrome: Results of a long‐term open‐label extension trial

Temporal pole epilepsy: Do not forget to look for occult encephaloceles

Fenfluramine significantly reduces day‐to‐day seizure burden by increasing number of seizure‐free days and time between seizures in patients with Dravet syndrome: A time‐to‐event analysis

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

Epilepsy and cannabidiol: a guide to treatment

Adverse effects of cannabinoids

Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox–Gastaut syndrome: Interim analysis of an open‐label extension study

Comprehensive scoping review of fenfluramine's role in managing generalized tonic–clonic seizures in developmental and epileptic encephalopathies

Long‐term evaluation of anterior thalamic deep brain stimulation for epilepsy in the European MORE registry

The burden of epilepsy and unmet need in people with focal seizures

GPI‐anchoring disorders and the heart: Is cardiomyopathy an overlooked feature?

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

Epileptogenic focal lesions in Dravet syndrome: A warning to investigators

Anterior midcingulate epilepsy: When semiology is of paramount importance to find the needle in the haystack

An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real‐world practice setting: A report from the Fenfluramine European Early Access Program

Hippocampal sclerosis caused by repetitive parieto‐insular seizures through a possible kindling mechanism

Spanish consensus on the management of concomitant antiseizure medications when using cenobamate in adults with drug‐resistant focal seizures

Consensus statement for the management of generalized tonic‐clonic seizures in Spain

Corticospinal tract displacement due to a large malformation during cortical development

Efficacy and tolerability of add-on stiripentol in real-world clinical practice: An observational study in Dravet syndrome and non-Dravet developmental and epileptic encephalopathies

Effect of fenfluramine on seizures and comorbidities in SCN8A‐developmental and epileptic encephalopathy: A case series

Patient profile, management, and quality of life associated with Dravet syndrome: a cross-sectional, multicentre study of 80 patients in Spain

Genetic (idiopathic) generalized epilepsy with occipital semiology

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

Testing patients during seizures: A European consensus procedure developed by a joint taskforce of the ILAE – Commission on European Affairs and the European Epilepsy Monitoring Unit Association

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