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A computational study of stimulus driven epileptic seizure abatement

PloS one, 2014-12, Vol.9 (12), p.e114316-e114316

2014

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Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

PLoS genetics, 2010-05, Vol.6 (5), p.e1000962-e1000962

2010

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Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood

American journal of human genetics, 2018-04, Vol.102 (4), p.557-573

2018

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Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish

Nature communications, 2019-02, Vol.10 (1), p.708-708, Article 708

2019

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Changes in activity of striato–thalamo–cortical network precede generalized spike wave discharges

NeuroImage (Orlando, Fla.), 2008-02, Vol.39 (4), p.1839-1849

2008

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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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Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly

Human molecular genetics, 2015-04, Vol.24 (8), p.2218-2227

2015

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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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EEG‐fMRI in atypical benign partial epilepsy

Epilepsia (Copenhagen), 2013-08, Vol.54 (8), p.e103-e108

2013

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EEG-MEG Integration Enhances the Characterization of Functional and Effective Connectivity in the Resting State Network

PloS one, 2015-10, Vol.10 (10), p.e0140832-e0140832

2015

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Folker Hanefeld, 1937-2022

European journal of paediatric neurology, 2022-07, Vol.39, p.A1-A2

2022

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Kindheit und Entwicklung – 30 Jahre

Kindheit und Entwicklung, 2021-01, Vol.30 (1), p.1-3

2021

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FIRES: Febrile infection responsive epileptic (FIRE) encephalopathies of school age

Brain & development (Tokyo. 1979), 2009-01, Vol.31 (1), p.91-91

2009

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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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Increased brain lactate during stroke-like episode in a patient with congenital disorder of glycosylation type Ia

Brain & development (Tokyo. 1979), 2009-02, Vol.31 (2), p.183-183

2009

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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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Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical Trial

JAMA neurology, 2020-03, Vol.77 (3), p.300

2020

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De novo variants in neurodevelopmental disorders with epilepsy

Nature genetics, 2018-07, Vol.50 (7), p.1048-1053

2018

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Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial

The Lancet (British edition), 2019-12, Vol.394 (10216), p.2243-2254

2019

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Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy

Journal of medical genetics, 2016-08, Vol.53 (8), p.511-522

2016

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A computational study of stimulus driven epileptic seizure abatement

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood

A multicenter, matched case‐control analysis comparing burden‐of‐illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany

Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish

Changes in activity of striato–thalamo–cortical network precede generalized spike wave discharges

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

Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly

Neuronal Networks during Burst Suppression as Revealed by Source Analysis

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

PRRT2 Mutations are the major cause of benign familial infantile seizures

EEG‐fMRI in atypical benign partial epilepsy

EEG-MEG Integration Enhances the Characterization of Functional and Effective Connectivity in the Resting State Network

Folker Hanefeld, 1937-2022

Kindheit und Entwicklung – 30 Jahre

FIRES: Febrile infection responsive epileptic (FIRE) encephalopathies of school age

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

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

Increased brain lactate during stroke-like episode in a patient with congenital disorder of glycosylation type Ia

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

Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical Trial

De novo variants in neurodevelopmental disorders with epilepsy

Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial

Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy

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