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Liesbet Deprez

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Sarah Weckhuysen; Simone Yendle; Iglika Yordanova; Dominique Audenaert; Samuel F Berkovic; Berten Ceulemans; Lieve R F Claes; Tine Deconinck; Liesbet Deprez; Danièle Hasaerts; Sarah E Heron; Dimitrina Hristova; An Jansen; Albena Jordanova; Lieven Lagae; Simone Mandelstam; John C Mulley; Filip Roelens; Ingrid E Scheffer; Katrien Smets; Thorsten Stanley; Arvid Suls; Peter de Jonghe
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Liesbet Deprez; S Weckhuysen; P Holmgren; Arvid Suls; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; A Jansen; K Verhaert; Lieven Lagae; Albena Jordanova; R Van Coster; S Yendle; Samuel F Berkovic; I Scheffer; Berten Ceulemans; Peter De Jonghe
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations.
Arvid Suls; R Velizarova; I Yordanova; Liesbet Deprez; Tine Van Dyck; Jan Wauters; Velina Guergueltcheva; L R F Claes; I Kremensky; Albena Jordanova; Peter De Jonghe
Four generations of epilepsy caused by an inherited microdeletion of the SCN1A gene.

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All Publications

2012: Sarah Weckhuysen; Simone Yendle; Iglika Yordanova; Dominique Audenaert; Samuel F Berkovic; Berten Ceulemans; Lieve R F Claes; Tine Deconinck; Liesbet Deprez; Danièle Hasaerts; Sarah E Heron; Dimitrina Hristova; An Jansen; Albena Jordanova; Lieven Lagae; Simone Mandelstam; John C Mulley; Filip Roelens; Ingrid E Scheffer; Katrien Smets; Thorsten Stanley; Arvid Suls; Peter de Jonghe
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Annals of neurology 2012;71(1):15-25.
2010: Liesbet Deprez; S Weckhuysen; P Holmgren; Arvid Suls; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; A Jansen; K Verhaert; Lieven Lagae; Albena Jordanova; R Van Coster; S Yendle; Samuel F Berkovic; I Scheffer; Berten Ceulemans; Peter De Jonghe
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations.
Neurology 2010;75(13):1159-65.
2010: Arvid Suls; R Velizarova; I Yordanova; Liesbet Deprez; Tine Van Dyck; Jan Wauters; Velina Guergueltcheva; L R F Claes; I Kremensky; Albena Jordanova; Peter De Jonghe
Four generations of epilepsy caused by an inherited microdeletion of the SCN1A gene.
Neurology 2010;75(1):72-6.
2009: Liesbet Deprez; An Jansen; Peter De Jonghe
Genetics of epilepsy syndromes starting in the first year of life.
Neurology 2009;72(3):273-81.
2008: Arvid Suls; Peter Dedeken; Karolien Goffin; Hilde Van Esch; Patrick Dupont; David Cassiman; Judith Kempfle; Thomas V Wuttke; Yvonne Weber; Holger Lerche; Zaid Afawi; Wim Vandenberghe; Amos D Korczyn; Samuel F Berkovic; Dana Ekstein; Sara Kivity; Philippe Ryvlin; Lieve R F Claes; Liesbet Deprez; Snezana Maljevic; Alberto Vargas; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; Koen Van Laere; Peter De Jonghe; Wim Van Paesschen
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
Brain : a journal of neurology 2008;131(Pt 7):1831-44.
2008: Liesbet Deprez; Sarah Weckhuysen; Karin Peeters; Tine Deconinck; Kristl G Claeys; Lieve R F Claes; Arvid Suls; Tine Van Dyck; André Palmini; Gert Matthijs; Wim Van Paesschen; Peter De Jonghe
Epilepsy as part of the phenotype associated with ATP1A2 mutations.
Epilepsia 2008;49(3):500-8.
2007: Liesbet Deprez; Karin Peeters; Wim Van Paesschen; Kristl G Claeys; Lieve R F Claes; Arvid Suls; Dominique Audenaert; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; Peter De Jonghe
Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q.
Neurology 2007;68(23):1995-2002.
2006: Arvid Suls; Kristl G Claeys; Dirk Goossens; Boris Harding; Rob van Luijk; Stefaan Scheers; Liesbet Deprez; Dominique Audenaert; Tine Van Dyck; Sabine Beeckmans; Iris Smouts; Berten Ceulemans; Lieven Lagae; Gunnar Buyse; Nina Barisic; Jean-Paul Misson; Jan Wauters; Jurgen Del-Favero; Peter De Jonghe; Lieve R F Claes
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.
Human mutation 2006;27(9):914-20.
2006: Dominique Audenaert; E Schwartz; Kristl G Claeys; Lieve R F Claes; Liesbet Deprez; Arvid Suls; Tine Van Dyck; Lieven Lagae; Christine Van Broeckhoven; R L Macdonald; Peter De Jonghe
A novel GABRG2 mutation associated with febrile seizures.
Neurology 2006;67(4):687-90.
2006: Nathalie Verpoorten; Kristl G Claeys; Liesbet Deprez; An Jacobs; Veerle Van Gerwen; Lieven Lagae; W F M Arts; Linda De Meirleir; Kathelijn Keymolen; Chantal Ceuterick-de Groote; Peter De Jonghe; Vincent Timmerman; Eva Nelis
Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV.
Neuromuscular disorders : NMD 2006;16(1):19-25.
2006: Liesbet Deprez; Lieve R F Claes; Kristl G Claeys; Dominique Audenaert; Tine Van Dyck; Dirk Goossens; Wim Van Paesschen; Jurgen Del-Favero; Christine Van Broeckhoven; Peter De Jonghe
Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation.
Human genetics 2006;118(5):618-25.
2005: Dominique Audenaert; Lieve R F Claes; Kristl G Claeys; Liesbet Deprez; Tine Van Dyck; Dirk Goossens; Jurgen Del-Favero; Wim Van Paesschen; Christine Van Broeckhoven; Peter De Jonghe
A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus.
Journal of medical genetics 2005;42(12):947-52.
2004: Lieve R F Claes; Berten Ceulemans; Dominique Audenaert; Liesbet Deprez; A Jansen; D Hasaerts; Stefan Weckx; Kristl G Claeys; Jurgen Del-Favero; Christine Van Broeckhoven; Peter De Jonghe
De novo KCNQ2 mutations in patients with benign neonatal seizures.
Neurology 2004;63(11):2155-8.
2004: Lieve R F Claes; Dominique Audenaert; Liesbet Deprez; Wim Van Paesschen; C Depondt; Dirk Goossens; Jurgen Del-Favero; Christine Van Broeckhoven; Peter De Jonghe
Novel locus on chromosome 12q22-q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures.
Journal of medical genetics 2004;41(9):710-4.