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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome

Epilepsia (Copenhagen), 2015-12, Vol.56 (12), p.e203-e208

2015

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Dynamic imaging of coherent sources reveals different network connectivity underlying the generation and perpetuation of epileptic seizures

PloS one, 2013-10, Vol.8 (10), p.e78422-e78422

2013

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Neuronal Networks during Burst Suppression as Revealed by Source Analysis

PloS one, 2015-04, Vol.10 (4), p.e0123807-e0123807

2015

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Seizure and cognitive outcomes of epilepsy surgery in infancy and early childhood

European journal of paediatric neurology, 2013-09, Vol.17 (5), p.498-506

2013

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The Natural History of Myoclonic Astatic Epilepsy (Doose Syndrome) and Lennox‐Gastaut Syndrome

Epilepsia (Copenhagen), 2006-11, Vol.47 (s2), p.53-55

Stephani, Ulrich

2006

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Simultaneous EEG and fMRI recordings (EEG‐fMRI) in children with epilepsy

Epilepsia (Copenhagen), 2013-06, Vol.54 (6), p.971-982

2013

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Efficacy and safety of corticosteroids and ACTH in epileptic syndromes beyond Infantile Epileptic Spasms Syndrome (IESS): A systematic review and meta‐analysis

Epilepsia (Copenhagen), 2024-05, Vol.65 (5), p.1155-1175

2024

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Developmental outcomes in children/adolescents and one adult with tuberous sclerosis complex (TSC) and refractory epilepsy treated with everolimus

Epilepsy & behavior, 2020-10, Vol.111, p.107182-107182, Article 107182

2020

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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

Nature genetics, 2015-04, Vol.47 (4), p.393-399

2015

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Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures

Epilepsia (Copenhagen), 2020-05, Vol.61 (5), p.995-1007

2020

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Long‐term seizure outcome in 211 patients with focal cortical dysplasia

Epilepsia (Copenhagen), 2015-01, Vol.56 (1), p.66-76

2015

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A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy

American journal of human genetics, 2019-06, Vol.104 (6), p.1060-1072

2019

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Costs of epilepsy and cost‐driving factors in children, adolescents, and their caregivers in Germany

Epilepsia (Copenhagen), 2015-09, Vol.56 (9), p.1388-1397

2015

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Quality of life and correlating factors in children, adolescents with epilepsy, and their caregivers: A cross-sectional multicenter study from Germany

Seizure (London, England), 2019-07, Vol.69, p.92-98

2019

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Variability of the hemodynamic response as a function of age and frequency of epileptic discharge in children with epilepsy

NeuroImage (Orlando, Fla.), 2008-04, Vol.40 (2), p.601-614

2008

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Seizure control and developmental trajectories after hemispherotomy for refractory epilepsy in childhood and adolescence

Epilepsia (Copenhagen), 2013-06, Vol.54 (6), p.1046-1055

2013

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Reoperation for Refractory Epilepsy in Childhood: A Second Chance for Selected Patients

Neurosurgery, 2013-10, Vol.73 (4), p.695-704

2013

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Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening

Molecular genetics and metabolism, 2014-03, Vol.111 (3), p.342-352

2014

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Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotype

European journal of medical genetics, 2015-08, Vol.58 (8), p.419-425

2015

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Fibration, fibrillation, and fasciculation: Say what you see

Clinical neurophysiology, 2007-06, Vol.118 (6), p.1418-1420

2007

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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome

Dynamic imaging of coherent sources reveals different network connectivity underlying the generation and perpetuation of epileptic seizures

Neuronal Networks during Burst Suppression as Revealed by Source Analysis

PRRT2 Mutations are the major cause of benign familial infantile seizures

Seizure and cognitive outcomes of epilepsy surgery in infancy and early childhood

The Natural History of Myoclonic Astatic Epilepsy (Doose Syndrome) and Lennox‐Gastaut Syndrome

Simultaneous EEG and fMRI recordings (EEG‐fMRI) in children with epilepsy

Efficacy and safety of corticosteroids and ACTH in epileptic syndromes beyond Infantile Epileptic Spasms Syndrome (IESS): A systematic review and meta‐analysis

Developmental outcomes in children/adolescents and one adult with tuberous sclerosis complex (TSC) and refractory epilepsy treated with everolimus

The phenotypic spectrum of SCN8A encephalopathy

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures

Long‐term seizure outcome in 211 patients with focal cortical dysplasia

De novo mutations in HCN1 cause early infantile epileptic encephalopathy

A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy

Costs of epilepsy and cost‐driving factors in children, adolescents, and their caregivers in Germany

Quality of life and correlating factors in children, adolescents with epilepsy, and their caregivers: A cross-sectional multicenter study from Germany

Variability of the hemodynamic response as a function of age and frequency of epileptic discharge in children with epilepsy

DNM1 encephalopathy: A new disease of vesicle fission

Seizure control and developmental trajectories after hemispherotomy for refractory epilepsy in childhood and adolescence

Reoperation for Refractory Epilepsy in Childhood: A Second Chance for Selected Patients

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening

Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotype

Fibration, fibrillation, and fasciculation: Say what you see

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