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Randomized phase III study 306: adjunctive perampanel for refractory partial-onset seizures

Neurology, 2012-05, Vol.78 (18), p.1408-1415

2012

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Long-term safety and efficacy of eslicarbazepine acetate in patients with focal seizures: Results of the 1-year ESLIBASE retrospective study

Epilepsy research, 2014-09, Vol.108 (7), p.1243-1252

2014

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GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

Neurology, 2012-02, Vol.78 (8), p.557-562

2012

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Safety and tolerability of perampanel: a review of clinical trial data

Acta neurologica Scandinavica, 2013-04, Vol.127 (s197), p.30-35

2013

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Safety, efficacy and outcome-related factors of perampanel over 12 months in a real-world setting: The FYDATA study

Epilepsy research, 2016-10, Vol.126, p.201-210

2016

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Lafora disease due to EPM2B mutations: a clinical and genetic study

Neurology, 2005-03, Vol.64 (6), p.982-986

2005

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Hepatic disease as the first manifestation of progressive myoclonus epilepsy of Lafora

Neurology, 2007-04, Vol.68 (17), p.1369-1373

2007

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A Novel Protein Tyrosine Phosphatase Gene Is Mutated in Progressive Myoclonus Epilepsy of the Lafora Type (EPM2)

Human molecular genetics, 1999-02, Vol.8 (2), p.345-352

1999

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Variant Intestinal-Cell Kinase in Juvenile Myoclonic Epilepsy

The New England journal of medicine, 2018-03, Vol.378 (11), p.1018-1028

2018

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Effect of lamotrigine on sexual function in patients with epilepsy

Seizure (London, England), 2006-04, Vol.15 (3), p.142-149

2006

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EFFICACY AND SAFETY OF ESLICARBAZEPINE-ACETATE IN ELDERLY PATIENTS WITH FOCAL EPILEPSY: CASE SERIES

Seizure (London, England), 2017-05, Vol.48, p.53-56

2017

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Socio-occupational and employment profile of patients with epilepsy

Epilepsy & behavior, 2011-07, Vol.21 (3), p.223-227

2011

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Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation

Journal of medical genetics, 2006-03, Vol.43 (3), p.232-237

2006

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Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients

Molecular genetics & genomic medicine, 2016-09, Vol.4 (5), p.568-580

2016

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Strategies to detect adverse effects of antiepileptic drugs in clinical practice

Epilepsy & behavior, 2008-07, Vol.13 (1), p.178-183

2008

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Arrangement and Mobility of Water in Vermiculite Hydrates Followed by 1H NMR Spectroscopy

The journal of physical chemistry. B, 2006-04, Vol.110 (15), p.7813-7819

2006

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Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11 : linkage to convulsions and electroencephalography trait

American journal of human genetics, 1995-08, Vol.57 (2), p.368-381

1995

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Adsorption of monovalent organic cations on sepiolite : Experimental results and model calculations

Clays and clay minerals, 1998-06, Vol.46 (3), p.340-348

1998

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Cortical myoclonus in angelman syndrome

Annals of neurology, 1996-07, Vol.40 (1), p.39-48

1996

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Novel mutation in STXBP1 gene in a patient with non-lesional Ohtahara syndrome

Neurologia (Barcelona, Spain), 2016-10, Vol.31 (8), p.523

2016

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Laforin, the dual-phosphatase responsible for Lafora disease, interacts with R5 (PTG), a regulatory subunit of protein phosphatase-1 that enhances glycogen accumulation

Human molecular genetics, 2003-12, Vol.12 (23), p.3161-3171

2003

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Onset of efficacy and adverse events during Cenobamate titration period

Acta neurologica Scandinavica, 2022-09, Vol.146 (3), p.265-275

2022

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Self-reported memory problems in everyday activities in patients with epilepsy treated with antiepileptic drugs

Epilepsy & behavior, 2009-04, Vol.14 (4), p.622-627

2009

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The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q

Human molecular genetics, 1995-09, Vol.4 (9), p.1657-1663

1995

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Randomized phase III study 306: adjunctive perampanel for refractory partial-onset seizures

Long-term safety and efficacy of eslicarbazepine acetate in patients with focal seizures: Results of the 1-year ESLIBASE retrospective study

GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

Safety and tolerability of perampanel: a review of clinical trial data

Safety, efficacy and outcome-related factors of perampanel over 12 months in a real-world setting: The FYDATA study

Lafora disease due to EPM2B mutations: a clinical and genetic study

Hepatic disease as the first manifestation of progressive myoclonus epilepsy of Lafora

A Novel Protein Tyrosine Phosphatase Gene Is Mutated in Progressive Myoclonus Epilepsy of the Lafora Type (EPM2)

Variant Intestinal-Cell Kinase in Juvenile Myoclonic Epilepsy

Effect of lamotrigine on sexual function in patients with epilepsy

EFFICACY AND SAFETY OF ESLICARBAZEPINE-ACETATE IN ELDERLY PATIENTS WITH FOCAL EPILEPSY: CASE SERIES

Socio-occupational and employment profile of patients with epilepsy

Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation

Erratum to “Safety, efficacy and outcome-related factors of perampanel over 12months in a real-world setting: The FYDATA study” [Epilepsy Res. 126 (2016) 201–210]

Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients

Strategies to detect adverse effects of antiepileptic drugs in clinical practice

Arrangement and Mobility of Water in Vermiculite Hydrates Followed by 1H NMR Spectroscopy

Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11 : linkage to convulsions and electroencephalography trait

Adsorption of monovalent organic cations on sepiolite : Experimental results and model calculations

Cortical myoclonus in angelman syndrome

Novel mutation in STXBP1 gene in a patient with non-lesional Ohtahara syndrome

Laforin, the dual-phosphatase responsible for Lafora disease, interacts with R5 (PTG), a regulatory subunit of protein phosphatase-1 that enhances glycogen accumulation

Onset of efficacy and adverse events during Cenobamate titration period

Self-reported memory problems in everyday activities in patients with epilepsy treated with antiepileptic drugs

The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q

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