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Sudden cardiac arrest in people with epilepsy in the community: Circumstances and risk factors.

• Robert J. Lamberts, Marieke Tabo Blom, +6 authors Hanno L. Tan
• Neurology
• 2015

OBJECTIVE To ascertain whether characteristics of ventricular tachycardia/fibrillation (VT/VF) differed between people with epilepsy and those without and which individuals with epilepsy were at… (More)

Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13.

• Dalila Pinto, Birgit Westland, +6 authors Bobby P. C. Koeleman
• Human molecular genetics
• 2005

Photoparoxysmal response (PPR) is an abnormal visual sensitivity of the brain in reaction to intermittent photic stimulation. It is an epilepsy-related electroencephalographic trait with high… (More)

Teaching Video NeuroImages: Frontal opercular seizures with jacksonian march.

• Jorunn Extercatte, Gerrit-Jan de Haan, Athanasios Gaitatzis
• Neurology
• 2015

A 31-year-old man presented with a 3-month history of progressive dysarthria and 1 month of gradually worsening motor seizures predominantly affecting the right face. Examination was unremarkable… (More)

Patterns of peripapillary retinal nerve fiber layer thinning in vigabatrin-exposed individuals.

• Lisa M. S. Clayton, Marita Dévilé, +4 authors Sanjay M. Sisodiya
• Ophthalmology
• 2012

PURPOSE To explore the relationship of peripapillary retinal nerve fiber layer (ppRNFL) thinning in individuals exposed to the antiepileptic drug vigabatrin with respect to 2 separate variables:… (More)

Gene symbol: KCNQ2. Disease: Benign neonatal familial convulsion.

• D. Pinto, Gerrit-Jan de Haan, +10 authors Darrin A Lindhout
• Human genetics
• 2005

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

• Michael Steffens, Costin Leu, +87 authors Thomas Sander
• Human molecular genetics
• 2012

Genetic generalized epilepsies (GGEs) have a lifetime prevalence of 0.3% and account for 20-30% of all epilepsies. Despite their high heritability of 80%, the genetic factors predisposing to GGEs… (More)

A novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 years.

• Gerrit-Jan de Haan, Dalila Pinto, +11 authors Dick Lindhout
• Epilepsia
• 2006

PURPOSE A large multigenerational family with benign familial neonatal convulsions (BFNC) was revisited to identify the disease-causing mutation and to assess long-term outcome. METHODS We… (More)

Monozygous twin brothers discordant for photosensitive epilepsy: first report of possible visual priming in humans.

• Gerrit-Jan de Haan, Dorothée G. A. Kasteleijn-Nolst Trenité, +5 authors E. H. Bertram
• Epilepsia
• 2005

PURPOSE The interaction of genetic predisposition and the environment in the development of epilepsy is often discussed, but, aside from some animal reflex epilepsies, little evidence supports such… (More)

Univerricht-Lundborg disease: underdiagnosed in the Netherlands.

• Gerrit-Jan de Haan, Dicky J J Halley, +10 authors Dick Lindhout
• Epilepsia
• 2004

PURPOSE Univerricht-Lundborg disease (ULD), with its major symptom of action myoclonus, is supposed to be very rare in the Netherlands and western Europe. We hypothesized that the syndrome may be… (More)

Epidemiology, pathophysiology and putative genetic basis of carbamazepine- and oxcarbazepine-induced hyponatremia.

• Bree D Berghuis, Gerrit-Jan de Haan, Marianne van den Broek, J. W. Sander, Dick Lindhout, B. P. C. Koeleman
• European journal of neurology
• 2016

The use of carbamazepine (CBZ) and oxcarbazepine (OXC) as first-line antiepileptic drugs in the treatment of focal epilepsy is limited by hyponatremia, a known adverse effect. Hyponatremia occurs in… (More)

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