Publications by authors named "Lieve Claes"

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KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Dominique Audenaert, Tine Deconinck, Lieve R F Claes

Ann Neurol· January 2012

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Non-fragrance allergens in specific cosmetic products.
Ana Rita Travassos, Lieve Claes, Lies Boey, Jacques Drieghe, An Goossens

Contact Dermatitis· November 2011

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Fragrance allergens in 'specific' cosmetic products.
Andrea Nardelli, Jacques Drieghe, Lieve Claes, Lies Boey, An Goossens

Contact Dermatitis· April 2011

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Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy.
Yunxiang Liao, Liesbet Deprez, Snezana Maljevic, Julika Pitsch, Lieve Claes

Brain· May 2010

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The SCN1A variant database: a novel research and diagnostic tool.
Lieve R F Claes, Liesbet Deprez, Arvid Suls, Jonathan Baets, Katrien Smets

Hum Mutat· October 2009

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A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
Nanda A Singh, Chris Pappas, E Jill Dahle, Lieve R F Claes, Timothy H Pruess

PLoS Genet· September 2009

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Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1.
Arvid Suls, Saul A Mullen, Yvonne G Weber, Kristien Verhaert, Berten Ceulemans, Lieve R F Claes

Ann Neurol· September 2009

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A functional null mutation of SCN1B in a patient with Dravet syndrome.
Gustavo A Patino, Lieve R F Claes, Luis F Lopez-Santiago, Emily A Slat, Raja S R Dondeti

J Neurosci· August 2009

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[Clinical and genetic diagnosis of Dravet syndrome: report of 20 cases].
Zsuzsa Siegler, Magdolna Neuwirth, Márta Hegyi, Eva Paraicz, Beatrix Pálmafy, Lieve Claes

Ideggyogy Sz· November 2008

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Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
Arvid Suls, Peter Dedeken, Karolien Goffin, Hilde Van Esch, Patrick Dupont, Lieve R F Claes

Brain· July 2008

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Epilepsy as part of the phenotype associated with ATP1A2 mutations.
Liesbet Deprez, Sarah Weckhuysen, Katelijne Peeters, Tine Deconinck, Kristl G Claeys, Lieve R F Claes

Epilepsia· March 2008

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Epilepsy and migraine in a patient with Urbach-Wiethe disease.
Kristl G Claeys, Lieve R F Claes, Johan W M Van Goethem, Sandy Sercu, Joseph Merregaert

Seizure· July 2007

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Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.
Arvid Suls, Kristl G Claeys, Dirk Goossens, Boris Harding, Rob Van Luijk, Lieve R F Claes

Hum Mutat· September 2006

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Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2.
Jennifer A Kearney, Yan Yang, Barbara Beyer, Sarah K Bergren, Lieve Claes

Hum Mol Genet· March 2006

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Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation.
Liesbet Deprez, Lieve R F Claes, Kristl G Claeys, Dominique Audenaert, Tine Van Dyck

Hum Genet· January 2006

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novoSNP, a novel computational tool for sequence variation discovery.
Stefan Weckx, Jurgen Del-Favero, Rosa Rademakers, Lieve Claes, Marc Cruts

Genome Res· March 2005

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Severe myoclonic epilepsy in infancy: toward an optimal treatment.
Berten Ceulemans, Marc Boel, Lieve Claes, Lina Dom, Herman Willekens

J Child Neurol· July 2004

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Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy.
Berten P G M Ceulemans, Lieve R F Claes, Lieven G Lagae

Pediatr Neurol· April 2004

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De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.
Lieve Claes, Berten Ceulemans, Dominique Audenaert, Katrien Smets, Ann Löfgren

Hum Mutat· June 2003

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