International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions

FDG-PET assessment and metabolic patterns in Lafora disease

(2020) Lorenzo Muccioli et al.   EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING

Assessment of the Predictive Value of Outpatient Smartphone Videos for Diagnosis of Epileptic Seizures

(2020) William O. Tatum et al.   JAMA Neurology

Acute symptomatic seizures secondary to autoimmune encephalitis and autoimmune‐associated epilepsy: Conceptual definitions

(2020) Claude Steriade et al.   EPILEPSIA

Prevention of Epilepsy in Infants with Tuberous Sclerosis Complex in the EPISTOP Trial

(2020) Katarzyna Kotulska et al.   ANNALS OF NEUROLOGY

Clinical features of sleep-related hypermotor epilepsy in relation to the seizure-onset zone: A review of 135 surgically treated cases

(2019) Steve A. Gibbs et al.   EPILEPSIA

Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients

(2019) Laura Licchetta et al.   SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

Mutations in MICAL-1 cause autosomal-dominant lateral temporal epilepsy

(2018) Emanuela Dazzo et al.   ANNALS OF NEUROLOGY

Update on Pharmacological Treatment of Progressive Myoclonus Epilepsies

(2018) Edoardo Ferlazzo et al.   CURRENT PHARMACEUTICAL DESIGN

Epilepsy with auditory features: Long-term outcome and predictors of terminal remission

(2018) Francesca Bisulli et al.   EPILEPSIA

Study of Intraventricular Cerliponase Alfa for CLN2 Disease

(2018) Angela Schulz et al.   NEW ENGLAND JOURNAL OF MEDICINE

Phenotypic spectrum in families with mesial temporal lobe epilepsy probands

(2018) Emilija Cvetkovska et al.   SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

Profile of neuropsychological impairment in Sleep-related Hypermotor Epilepsy

(2018) Laura Licchetta et al.   SLEEP MEDICINE

Evaluation of dual pathology among drug-resistant epileptic patients with hippocampal sclerosis

(2018) Jafar Mehvari Habibabadi et al.   NEUROLOGICAL SCIENCES

Genetics of Focal Epilepsies: What Do We Know and Where Are We Heading?

(2018) Piero Perucca   Epilepsy Currents

Photosensitivity is an early marker of neuronal ceroid lipofuscinosis type 2 disease

(2017) Nicola Specchio et al.   EPILEPSIA

Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology

(2017) Robert S. Fisher et al.   EPILEPSIA

The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations

(2017) Roberto Michelucci et al.   EPILEPSY & BEHAVIOR

Prevalence and Incidence of Drug-Resistant Mesial Temporal Lobe Epilepsy in the United States

(2017) Ali A. Asadi-Pooya et al.   World Neurosurgery

Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex geneNPRL3

(2016) Georg-Christoph Korenke et al.   EPILEPSIA

Sleep-related hypermotor epilepsy

(2016) Laura Licchetta et al.   NEUROLOGY

Definition and diagnostic criteria of sleep-related hypermotor epilepsy

(2016) Paolo Tinuper et al.   NEUROLOGY

Lateralizing value of semiology in medial temporal lobe epilepsy

(2015) S. Dupont et al.   ACTA NEUROLOGICA SCANDINAVICA

Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy

(2015) Emanuela Dazzo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Familial focal epilepsy with focal cortical dysplasia due toDEPDC5mutations

(2015) Stéphanie Baulac et al.   ANNALS OF NEUROLOGY

Mutations in the mammalian target of rapamycin pathway regulatorsNPRL2andNPRL3cause focal epilepsy

(2015) Michael G. Ricos et al.   ANNALS OF NEUROLOGY

DEPDC5mutations are not a frequent cause of familial temporal lobe epilepsy

(2015) Pasquale Striano et al.   EPILEPSIA

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Refining the phenotype of Unverricht-Lundborg disease (EPM1): A population-wide Finnish study

(2015) J. Hypponen et al.   NEUROLOGY

Mutations in mammalian target of rapamycin regulatorDEPDC5cause focal epilepsy with brain malformations

(2014) Ingrid E. Scheffer et al.   ANNALS OF NEUROLOGY

Mild Lafora disease: Clinical, neurophysiologic, and genetic findings

(2014) Edoardo Ferlazzo et al.   EPILEPSIA

Drug-resistant focal sleep related epilepsy: Results and predictors of surgical outcome

(2014) Anna Losurdo et al.   EPILEPSY RESEARCH

Rasmussen's encephalitis: clinical features, pathobiology, and treatment advances

(2014) Sophia Varadkar et al.   LANCET NEUROLOGY

DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy

(2014) F. Picard et al.   NEUROLOGY

Hippocampal sclerosis after febrile status epilepticus: The FEBSTAT study

(2013) Darrell V. Lewis et al.   ANNALS OF NEUROLOGY

Clinical application and evaluation of the Bien diagnostic criteria for Rasmussen encephalitis

(2013) Heather E. Olson et al.   EPILEPSIA

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

(2013) Leanne M Dibbens et al.   NATURE GENETICS

Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy

(2013) Filippo Maria Santorelli et al.   Orphanet Journal of Rare Diseases

Familial focal epilepsy with variable foci mapped to chromosome 22q12: Expansion of the phenotypic spectrum

(2012) Karl Martin Klein et al.   EPILEPSIA

Rasmussen encephalitis: Incidence and course under randomized therapy with tacrolimus or intravenous immunoglobulins

(2012) Christian G. Bien et al.   EPILEPSIA

New observations in primary and secondary reading epilepsy: Excellent response to levetiracetam and early spontaneous remission

(2012) M. Ayman Haykal et al.   EPILEPSY & BEHAVIOR

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

(2012) Sarah E Heron et al.   NATURE GENETICS

LGI1microdeletion in autosomal dominant lateral temporal epilepsy

(2012) M. Fanciulli et al.   NEUROLOGY

MRI and EEG as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy

(2012) M. E. Morita et al.   NEUROLOGY

Kufs Disease, the Major Adult Form of Neuronal Ceroid Lipofuscinosis, Caused by Mutations in CLN6

(2011) Todor Arsov et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Insular-opercular seizures manifesting with sleep-related paroxysmal motor behaviors: A stereo-EEG study

(2011) Paola Proserpio et al.   EPILEPSIA

Reading epilepsy and its variants: A model for system epilepsy

(2011) Pasquale Striano et al.   EPILEPSY & BEHAVIOR

Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance

(2010) D. E. Crompton et al.   BRAIN

Progressive myoclonus epilepsy: genetic and nosological aspects with special reference to 107 Finnish patients

(2010) Reijo Norio et al.   CLINICAL GENETICS

The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission1

(2010) Ingmar Blümcke et al.   EPILEPSIA

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

(2010) Anne T. Berg et al.   EPILEPSIA

The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in Newfoundland

(2009) SJ Moore et al.   CLINICAL GENETICS

Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability

(2008) Christopher P. Derry et al.   EPILEPSIA

Childhood occipital epilepsy of Gastaut: A study of 33 patients

(2007) Roberto Horacio Caraballo et al.   EPILEPSIA