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

European journal of neurology, 2016-09, Vol.23 (9), p.1393-1399

2016

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Somatic mosaicism as a basic epileptogenic mechanism?

Brain (London, England : 1878), 2008-04, Vol.131 (4), p.900-901

Lindhout, Dick

2008

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Male patients affected by mosaic PCDH19 mutations: five new cases

Neurogenetics, 2017-07, Vol.18 (3), p.147-153

2017

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Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia

Journal of medical genetics, 2006-04, Vol.43 (4), p.371-377

2006

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Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

Cell, 1997-05, Vol.89 (5), p.773-779

1997

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Gestation-induced changes in lamotrigine pharmacokinetics: a monotherapy study

Neurology, 2004-08, Vol.63 (3), p.571-573

2004

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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

Cell, 1996-11, Vol.87 (3), p.543-552

1996

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Effect of oral contraceptives on lamotrigine levels depends on comedication

Acta neurologica Scandinavica, 2014-06, Vol.129 (6), p.393-398

2014

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Utilization of antiepileptic drugs during pregnancy: Comparative patterns in 38 countries based on data from the EURAP registry

Epilepsia (Copenhagen), 2009-10, Vol.50 (10), p.2305-2309

Battino, Dina

2009

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A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation

Neurology, 2009-01, Vol.72 (3), p.287-288

2009

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Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

Neurogenetics, 2013-02, Vol.14 (1), p.23-34

2013

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Co‐occurring intertidal ecosystem engineers with opposing growth strategies show opposite responses to environmental gradients during establishment

Oikos, 2024-07, Vol.2024 (7), p.n/a

2024

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Dose-dependent risk of malformations with antiepileptic drugs: an analysis of data from the EURAP epilepsy and pregnancy registry

Lancet neurology, 2011-07, Vol.10 (7), p.609-617

2011

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P1308 HEPATOPROTECTIVE EFFECTS OF NGM282 COMPARED TO OBETICHOLIC ACID AND BEZAFIBRATE IN MOUSE MODELS OF CHOLESTASIS

Journal of hepatology, 2014-04, Vol.60 (1), p.S531-S531

2014

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Maternal Use of Antiepileptic Drugs and the Risk of Major Congenital Malformations: A Joint European Prospective Study of Human Teratogenesis Associated with Maternal Epilepsy

Epilepsia (Copenhagen), 1997-09, Vol.38 (9), p.981-990

1997

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Antiepileptic drug regimens and major congenital abnormalities in the offspring

Annals of neurology, 1999-11, Vol.46 (5), p.739-746

1999

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Seizure control and treatment changes in pregnancy: Observations from the EURAP epilepsy pregnancy registry

Epilepsia (Copenhagen), 2013-09, Vol.54 (9), p.1621-1627

2013

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Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients

Human genetics, 2005-01, Vol.116 (1-2), p.8-16

2005

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Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis

Neurology, 2002-03, Vol.58 (5), p.702-708

2002

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Hyperactive behavior in a family with autosomal dominant lateral temporal lobe epilepsy caused by a mutation in the LGI1 /epitempin gene

Epilepsy & behavior, 2013-07, Vol.28 (1), p.41-46

2013

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MSH2 genomic deletions are a frequent cause of HNPCC

Nature genetics, 1998-12, Vol.20 (4), p.326-328

1998

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Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis

Epilepsy research, 2010-05, Vol.89 (2), p.286-294

2010

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Withdrawal of valproic acid treatment during pregnancy and seizure outcome: Observations from EURAP

Epilepsia (Copenhagen), 2016-08, Vol.57 (8), p.e173-e177

2016

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1508 Spectrum of Neural Tube Defects after Prenatal Antiepileptic Drug Exposure: Extensive Case Series

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A427-A428

2012

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Dose-dependent teratogenicity of valproate in mono- and polytherapy: an observational study

Neurology, 2015-09, Vol.85 (10), p.866-872

2015

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

Somatic mosaicism as a basic epileptogenic mechanism?

Male patients affected by mosaic PCDH19 mutations: five new cases

Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia

Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia

Gestation-induced changes in lamotrigine pharmacokinetics: a monotherapy study

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

Effect of oral contraceptives on lamotrigine levels depends on comedication

Utilization of antiepileptic drugs during pregnancy: Comparative patterns in 38 countries based on data from the EURAP registry

A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation

Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

Co‐occurring intertidal ecosystem engineers with opposing growth strategies show opposite responses to environmental gradients during establishment

Dose-dependent risk of malformations with antiepileptic drugs: an analysis of data from the EURAP epilepsy and pregnancy registry

P1308 HEPATOPROTECTIVE EFFECTS OF NGM282 COMPARED TO OBETICHOLIC ACID AND BEZAFIBRATE IN MOUSE MODELS OF CHOLESTASIS

Maternal Use of Antiepileptic Drugs and the Risk of Major Congenital Malformations: A Joint European Prospective Study of Human Teratogenesis Associated with Maternal Epilepsy

Antiepileptic drug regimens and major congenital abnormalities in the offspring

Seizure control and treatment changes in pregnancy: Observations from the EURAP epilepsy pregnancy registry

Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis

Hyperactive behavior in a family with autosomal dominant lateral temporal lobe epilepsy caused by a mutation in the LGI1 /epitempin gene

MSH2 genomic deletions are a frequent cause of HNPCC

Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis

Withdrawal of valproic acid treatment during pregnancy and seizure outcome: Observations from EURAP

1508 Spectrum of Neural Tube Defects after Prenatal Antiepileptic Drug Exposure: Extensive Case Series

Dose-dependent teratogenicity of valproate in mono- and polytherapy: an observational study

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