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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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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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Weight change associated with antiepileptic drugs

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

2013

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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

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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

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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

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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

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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

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Phospho‐STAT5 and phospho‐Akt expression in chronic myeloproliferative neoplasms

British journal of haematology, 2009-11, Vol.147 (4), p.495-506

2009

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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

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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

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Intra-operative cell salvage in pelvic and acetabular fracture surgery: a retrospective comparative study

International orthopaedics, 2019-07, Vol.43 (7), p.1695-1699

2019

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Long QT and Brugada syndrome gene mutations in New Zealand

Heart rhythm, 2007-10, Vol.4 (10), p.1306-1314

2007

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Biophysical Properties of 9 KCNQ1 Mutations Associated With Long-QT Syndrome

Circulation. Arrhythmia and electrophysiology, 2009-08, Vol.2 (4), p.417-426

2009

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Identifying and prioritising epilepsy treatment uncertainties

Journal of neurology, neurosurgery and psychiatry, 2010-08, Vol.81 (8), p.918-921

2010

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TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's disease

Brain research. Molecular brain research., 2004-06, Vol.125 (1), p.120-128

2004

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No evidence for allelic association between bipolar disorder and monoamine oxidase a gene polymorphisms

American journal of medical genetics, 1995-08, Vol.60 (4), p.322-324

1995

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Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13

Eye (London), 2000-04, Vol.14 (2), p.172-175

2000

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Efficacy and safety of prostate artery embolization for benign prostatic hyperplasia: an observational study and propensity‐matched comparison with transurethral resection of the prostate (the UK‐ROPE study)

BJU international, 2018-08, Vol.122 (2), p.270-282

2018

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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

Complement is activated in progressive multiple sclerosis cortical grey matter lesions

Weight change associated with antiepileptic drugs

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

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

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

Phospho‐STAT5 and phospho‐Akt expression in chronic myeloproliferative neoplasms

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

Intra-operative cell salvage in pelvic and acetabular fracture surgery: a retrospective comparative study

Long QT and Brugada syndrome gene mutations in New Zealand

Biophysical Properties of 9 KCNQ1 Mutations Associated With Long-QT Syndrome

Identifying and prioritising epilepsy treatment uncertainties

TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's disease

No evidence for allelic association between bipolar disorder and monoamine oxidase a gene polymorphisms

Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13

Efficacy and safety of prostate artery embolization for benign prostatic hyperplasia: an observational study and propensity‐matched comparison with transurethral resection of the prostate (the UK‐ROPE study)

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