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Epilepsy, antiepileptic drugs, and the risk of major cardiovascular events

Epilepsia (Copenhagen), 2021-07, Vol.62 (7), p.1604-1616

2021

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Sex-specific disease modifiers in juvenile myoclonic epilepsy

Scientific reports, 2022-02, Vol.12 (1), p.2785-2785, Article 2785

2022

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Meningeal inflammation and cortical demyelination in acute multiple sclerosis

Annals of neurology, 2018-12, Vol.84 (6), p.829-842

2018

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Dynamic changes in myelin aberrations and oligodendrocyte generation in chronic amyloidosis in mice and men

Glia, 2013-02, Vol.61 (2), p.273-286

2013

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Overlapping cortical malformations and mutations in TUBB2B and TUBA1A

Brain (London, England : 1878), 2013-02, Vol.136 (Pt 2), p.536-548

2013

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Complement is activated in progressive multiple sclerosis cortical grey matter lesions

Journal of neuroinflammation, 2016-06, Vol.13 (1), p.161-161, Article 161

2016

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Genetic influences on epilepsy outcomes: A whole‐exome sequencing and health care records data linkage study

Epilepsia (Copenhagen), 2023-11, Vol.64 (11), p.3099-3108

2023

Volltextzugriff (PDF)

Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay

Brain (London, England : 1878), 2013-10, Vol.136 (10), p.3085-3095

2013

Volltextzugriff (PDF)

Validating epilepsy diagnoses in routinely collected data

Seizure (London, England), 2017-11, Vol.52, p.195-198

2017

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Epilepsy and deprivation, a data linkage study

Epilepsia (Copenhagen), 2015-04, Vol.56 (4), p.585-591

2015

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Trends in the first antiepileptic drug prescribed for epilepsy between 2000 and 2010

Seizure (London, England), 2014-01, Vol.23 (1), p.77-80

2014

Volltextzugriff (PDF)

Long-term outcomes after epilepsy surgery, a retrospective cohort study linking patient-reported outcomes and routine healthcare data

Epilepsy & behavior, 2020-10, Vol.111, p.107196-107196, Article 107196

2020

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Misdiagnosis of Long QT Syndrome as Epilepsy at First Presentation

Annals of emergency medicine, 2009-07, Vol.54 (1), p.26-32

2009

Volltextzugriff (PDF)

Weight change associated with antiepileptic drugs

Journal of neurology, neurosurgery and psychiatry, 2013-07, Vol.84 (7), p.796-799

2013

Volltextzugriff (PDF)

Immunohistochemical staining of post-mortem adult human brain sections

Nature physics, 2007-01, Vol.1 (6), p.2719-2732

2007

Volltextzugriff (PDF)

The phenotype of bilateral hippocampal sclerosis and its management in “real life” clinical settings

Epilepsia (Copenhagen), 2018-07, Vol.59 (7), p.1410-1420

2018

Volltextzugriff (PDF)

Executive functions and psychiatric symptoms in drug-refractory juvenile myoclonic epilepsy

Epilepsy & behavior, 2014-06, Vol.35, p.72-77

2014

Volltextzugriff (PDF)

Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome

Heart rhythm, 2008-09, Vol.5 (9), p.1275-1281

2008

Volltextzugriff (PDF)

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

BMC medical genetics, 2016-04, Vol.17 (1), p.34, Article 34

2016

Volltextzugriff (PDF)

A Novel GABRG2 mutation, p.R136, in a family with GEFS + and extended phenotypes

Neurobiology of disease, 2014-04, Vol.64, p.131-141

2014

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Elevated serum gastrin levels in Jervell and Lange-Nielsen syndrome: A marker of severe KCNQ1 dysfunction?

Heart rhythm, 2011-04, Vol.8 (4), p.551-554

2011

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Glycine receptors in the striatum, globus pallidus, and substantia nigra of the human brain: An immunohistochemical study

Journal of comparative neurology (1911), 2007-06, Vol.502 (6), p.1012-1029

2007

Volltextzugriff (PDF)

Not All hERG Pore Domain Mutations Have a Severe Phenotype: G584S Has an Inactivation Gating Defect with Mild Phenotype Compared to G572S, Which Has a Dominant Negative Trafficking Defect and a Severe Phenotype

Journal of cardiovascular electrophysiology, 2009-08, Vol.20 (8), p.923-930

2009

Volltextzugriff (PDF)

Symptoms and Signs Associated with Syncope in Young People with Primary Cardiac Arrhythmias

Heart, lung & circulation, 2011-09, Vol.20 (9), p.593-598

2011

Volltextzugriff (PDF)

GLRB is the third major gene of effect in hyperekplexia

Human molecular genetics, 2013-03, Vol.22 (5), p.927-940

2013

Volltextzugriff (PDF)

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Epilepsy, antiepileptic drugs, and the risk of major cardiovascular events

Sex-specific disease modifiers in juvenile myoclonic epilepsy

Meningeal inflammation and cortical demyelination in acute multiple sclerosis

Dynamic changes in myelin aberrations and oligodendrocyte generation in chronic amyloidosis in mice and men

Overlapping cortical malformations and mutations in TUBB2B and TUBA1A

Complement is activated in progressive multiple sclerosis cortical grey matter lesions

Genetic influences on epilepsy outcomes: A whole‐exome sequencing and health care records data linkage study

Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay

Validating epilepsy diagnoses in routinely collected data

Epilepsy and deprivation, a data linkage study

Trends in the first antiepileptic drug prescribed for epilepsy between 2000 and 2010

Long-term outcomes after epilepsy surgery, a retrospective cohort study linking patient-reported outcomes and routine healthcare data

Misdiagnosis of Long QT Syndrome as Epilepsy at First Presentation

Weight change associated with antiepileptic drugs

Immunohistochemical staining of post-mortem adult human brain sections

The phenotype of bilateral hippocampal sclerosis and its management in “real life” clinical settings

Executive functions and psychiatric symptoms in drug-refractory juvenile myoclonic epilepsy

Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

A Novel GABRG2 mutation, p.R136, in a family with GEFS + and extended phenotypes

Elevated serum gastrin levels in Jervell and Lange-Nielsen syndrome: A marker of severe KCNQ1 dysfunction?

Glycine receptors in the striatum, globus pallidus, and substantia nigra of the human brain: An immunohistochemical study

Not All hERG Pore Domain Mutations Have a Severe Phenotype: G584S Has an Inactivation Gating Defect with Mild Phenotype Compared to G572S, Which Has a Dominant Negative Trafficking Defect and a Severe Phenotype

Symptoms and Signs Associated with Syncope in Young People with Primary Cardiac Arrhythmias

GLRB is the third major gene of effect in hyperekplexia

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