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Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia

Journal of neurology, 2016-02, Vol.263 (2), p.334-343

2016

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SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain

Neurology, 2010-10, Vol.75 (16), p.1454-1458

2010

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Long-term outcome in pyridoxine-responsive infantile epilepsy

European journal of paediatric neurology, 2015-11, Vol.19 (6), p.647-651

2015

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Normal intelligence in children with prenatal exposure to carbamazepine

Neurology, 2004-01, Vol.62 (1), p.28-32

2004

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Clinical and genetic spectrum of SCN2A-associated episodic ataxia

European journal of paediatric neurology, 2019-05, Vol.23 (3), p.438-447

2019

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Combined use of non-invasive techniques for improved functional localization for a selected group of epilepsy surgery candidates

NeuroImage (Orlando, Fla.), 2009-04, Vol.45 (2), p.342-348

2009

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Measuring spike strength in patients with continuous spikes and waves during sleep: Comparison of methods for prospective use as a clinical index

Clinical neurophysiology, 2014-08, Vol.125 (8), p.1639-1646

2014

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P11 – 2238: Long-term outcome in pyridoxine-responsive infantile epilepsy

European journal of paediatric neurology, 2015-05, Vol.19, p.S97-S97

2015

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Valproate in the treatment of epilepsy in girls and women of childbearing potential

Epilepsia (Copenhagen), 2015-07, Vol.56 (7), p.1006-1019

2015

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Semiautomatic quantification of spiking in patients with continuous spikes and waves in sleep: Sensitivity to settings and correspondence to visual assessment

Clinical neurophysiology, 2012-07, Vol.123 (7), p.1284-1290

2012

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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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Cognitive outcomes after fetal exposure to carbamazepine, lamotrigine, valproate or levetiracetam monotherapy: Data from the EURAP neurocognitive extension protocol

Epilepsy & behavior, 2024-10, Vol.159, p.110024, Article 110024

2024

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Proton Spectroscopic Imaging Shows Abnormalities in Glial and Neuronal Cell Pools in Frontal Lobe Epilepsy

Epilepsia (Copenhagen), 2001-12, Vol.42 (12), p.1507-1514

2001

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Asymmetric and Asynchronous Infantile Spasms

Epilepsia (Copenhagen), 1995-09, Vol.36 (9), p.873-882

1995

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Focal and global cortical hypometabolism in patients with newly diagnosed infantile spasms

Neurology, 2002-06, Vol.58 (11), p.1646-1651

2002

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Cognitive/behavioral teratogenetic effects of antiepileptic drugs

Epilepsy & behavior, 2007-11, Vol.11 (3), p.292-302

2007

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Oxcarbazepine in the treatment of epilepsy in children and adolescents with intellectual disability

Journal of intellectual disability research, 1998-12, Vol.42 Suppl 1, p.41-45

1998

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Navigated TMS for preoperative functional localization: initial experiences from five epilepsy patients

Brain stimulation, 2008, Vol.1 (3), p.303-303

2008

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Pons tumour behind a phenotypic Rett syndrome presentation

Developmental medicine and child neurology, 1998-12, Vol.40 (12), p.836-839

1998

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What can we say to women of reproductive age with epilepsy?

Neurology, 2005-03, Vol.64 (6), p.938-939

2005

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Low-grade gliomas and focal cortical developmental malformations: differentiation with proton MR spectroscopy

Radiology, 2004-03, Vol.230 (3), p.703-708

2004

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Head circumference in children of epileptic mothers: Contributions of drug exposure and genetic background

Epilepsy research, 1990-04, Vol.5 (3), p.217-222

1990

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Treatment of Infantile Spasms: Results of a Population‐Based Study with Vigabatrin as the First Drug for Spasms

Epilepsia (Copenhagen), 1999-07, Vol.40 (7), p.950-957

1999

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Two-Year Follow-Up of Intelligence After Pediatric Epilepsy Surgery

Pediatric neurology, 2005-09, Vol.33 (3), p.173-178

2005

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Infantile spasms: diagnosis and assessment of treatment response by video-EEG

Developmental medicine and child neurology, 2001-10, Vol.43 (10), p.658-667

2001

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Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia

SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain

Long-term outcome in pyridoxine-responsive infantile epilepsy

Normal intelligence in children with prenatal exposure to carbamazepine

Clinical and genetic spectrum of SCN2A-associated episodic ataxia

Combined use of non-invasive techniques for improved functional localization for a selected group of epilepsy surgery candidates

Measuring spike strength in patients with continuous spikes and waves during sleep: Comparison of methods for prospective use as a clinical index

P11 – 2238: Long-term outcome in pyridoxine-responsive infantile epilepsy

Valproate in the treatment of epilepsy in girls and women of childbearing potential

Semiautomatic quantification of spiking in patients with continuous spikes and waves in sleep: Sensitivity to settings and correspondence to visual assessment

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

Cognitive outcomes after fetal exposure to carbamazepine, lamotrigine, valproate or levetiracetam monotherapy: Data from the EURAP neurocognitive extension protocol

Proton Spectroscopic Imaging Shows Abnormalities in Glial and Neuronal Cell Pools in Frontal Lobe Epilepsy

Asymmetric and Asynchronous Infantile Spasms

Focal and global cortical hypometabolism in patients with newly diagnosed infantile spasms

Cognitive/behavioral teratogenetic effects of antiepileptic drugs

Oxcarbazepine in the treatment of epilepsy in children and adolescents with intellectual disability

Navigated TMS for preoperative functional localization: initial experiences from five epilepsy patients

Pons tumour behind a phenotypic Rett syndrome presentation

What can we say to women of reproductive age with epilepsy?

Low-grade gliomas and focal cortical developmental malformations: differentiation with proton MR spectroscopy

Head circumference in children of epileptic mothers: Contributions of drug exposure and genetic background

Treatment of Infantile Spasms: Results of a Population‐Based Study with Vigabatrin as the First Drug for Spasms

Two-Year Follow-Up of Intelligence After Pediatric Epilepsy Surgery

Infantile spasms: diagnosis and assessment of treatment response by video-EEG

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