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Epileptic activity in neurological deterioration after ischemic stroke, a continuous EEG study

Clinical neurophysiology, 2019-12, Vol.130 (12), p.2282-2286

2019

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Scale for the assessment and rating of ataxia: development of a new clinical scale

Neurology, 2006-06, Vol.66 (11), p.1717

2006

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The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study

Neurology, 2011-09, Vol.77 (11), p.1035

2011

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Validation of an algorithm of time-dependent electro-clinical risk stratification for electrographic seizures (TERSE) in critically ill patients

Clinical neurophysiology, 2020-08, Vol.131 (8), p.1956-1961

2020

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Responsiveness of different rating instruments in spinocerebellar ataxia patients

Neurology, 2010-02, Vol.74 (8), p.678

2010

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Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms

Neurology, 2008-09, Vol.71 (13), p.982

2008

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SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia

Neurology, 2008-08, Vol.71 (7), p.486

2008

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P88. Identification of genome-based biomarkers for response to specific antiepileptic drugs in focal and idiopathic generalized epilepsies

Clinical neurophysiology, 2015-08, Vol.126 (8), p.e146-e147

2015

Volltextzugriff (PDF)

Complexité et désordre: Éléments de réflexion

Lévy, Jean-Claude S

1, 2021

Volltextzugriff (PDF)

Pharmacogenetics in neuropsychiatric diseases : epilepsy as a model

Acta neurologica Belgica, 2006-12, Vol.106 (4), p.157-167

DEPONDT, C

2006

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Acute behavioural change in a young woman evolving towards cerebellar syndrome

Clinical neurology and neurosurgery, 2010-07, Vol.112 (6), p.509-511

2010

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The long term retention of levetiracetam in a large cohort of patients with epilepsy

Journal of neurology, neurosurgery and psychiatry, 2006-01, Vol.77 (1), p.101-103

2006

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Novel locus on chromosome 12q22–q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures

Journal of medical genetics, 2004-09, Vol.41 (9), p.710-714

2004

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No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy

Epilepsy research, 2009-01, Vol.83 (1), p.44-51

2009

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Familial temporal lobe epilepsy with febrile seizures

Neurology, 2002-05, Vol.58 (9), p.1429

2002

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Genetic Predictors of the Maximum Doses Patients Receive during Clinical Use of the Anti-Epileptic Drugs Carbamazepine and Phenytoin

Proceedings of the National Academy of Sciences - PNAS, 2005-04, Vol.102 (15), p.5507-5512

2005

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The potential of pharmacogenetics in the treatment of epilepsy

European journal of paediatric neurology, 2006-03, Vol.10 (2), p.57-65

Depondt, Chantal

2006

Volltextzugriff (PDF)

Selection and Evaluation of Tagging SNPs in the Neuronal-Sodium-Channel Gene SCN1A: Implications for Linkage-Disequilibrium Gene Mapping

American journal of human genetics, 2003-09, Vol.73 (3), p.551-565

2003

Volltextzugriff (PDF)

Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene

Genome research, 2004-07, Vol.14 (7), p.1333

2004

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Intestinal-Cell Kinase and Juvenile Myoclonic Epilepsy

The New England journal of medicine, 2019-04, Vol.380 (16), p.e24-1028

2019

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The -1021C->T DBH gene variant is not associated with epilepsy or antiepileptic drug response

Neurology, 2004-10, Vol.63 (8), p.1497

2004

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Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?

Brain (London, England : 1878), 2005-08, Vol.128 (8), p.1832-1840

2005

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Guidelines for the management of epilepsy in the elderly

Acta neurologica Belgica, 2006-09, Vol.106 (3), p.111-116

2006

Volltextzugriff (PDF)

A candidate gene study of antiepileptic drug tolerability and efficacy identifies an association of CYP2C9 variants with phenytoin toxicity: AED response candidate gene study

European journal of neurology, 2011-09, Vol.18 (9), p.1159-1164

2011

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Lack of replication of association between scn1a SNP and febrile seizures

Neurology, 2009-12, Vol.73 (22), p.1928

2009

Volltextzugriff (PDF)

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Epileptic activity in neurological deterioration after ischemic stroke, a continuous EEG study

Scale for the assessment and rating of ataxia: development of a new clinical scale

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study

Validation of an algorithm of time-dependent electro-clinical risk stratification for electrographic seizures (TERSE) in critically ill patients

Responsiveness of different rating instruments in spinocerebellar ataxia patients

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms

SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia

P88. Identification of genome-based biomarkers for response to specific antiepileptic drugs in focal and idiopathic generalized epilepsies

Complexité et désordre: Éléments de réflexion

Pharmacogenetics in neuropsychiatric diseases : epilepsy as a model

Acute behavioural change in a young woman evolving towards cerebellar syndrome

The long term retention of levetiracetam in a large cohort of patients with epilepsy

Novel locus on chromosome 12q22–q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures

No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy

Familial temporal lobe epilepsy with febrile seizures

Genetic Predictors of the Maximum Doses Patients Receive during Clinical Use of the Anti-Epileptic Drugs Carbamazepine and Phenytoin

The potential of pharmacogenetics in the treatment of epilepsy

Selection and Evaluation of Tagging SNPs in the Neuronal-Sodium-Channel Gene SCN1A: Implications for Linkage-Disequilibrium Gene Mapping

Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene

Intestinal-Cell Kinase and Juvenile Myoclonic Epilepsy

The -1021C->T DBH gene variant is not associated with epilepsy or antiepileptic drug response

Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?

Guidelines for the management of epilepsy in the elderly

A candidate gene study of antiepileptic drug tolerability and efficacy identifies an association of CYP2C9 variants with phenytoin toxicity: AED response candidate gene study

Lack of replication of association between scn1a SNP and febrile seizures

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