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Lagae, L.
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Issue Date
Title
Author(s)
Type
Cat.
2011
Screening for Cerebral Visual Impairment: Value of a CVI Questionnaire
Ortibus, E.
;
LAENEN, Annouschka
;
Verhoeven, J.
;
De Cock, P.
;
Casteels, I.
;
Schoolmeesters, B.
;
Buyck, A.
;
Lagae, L.
Journal Contribution
A1
2004
Clinical correlations of mutation in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy
Ceulemans, B.
;
CLAES, Lieve
;
Lagae, L.
Journal Contribution
A1
2004
Severe myoclonic epilepsy in infancy: towards an optimal treatment
Ceulemans, B.
;
Boel, M.
;
CLAES, Lieve
;
Dom, L.
;
Willekens, H.
;
Thiry, Ph.
;
Lagae, L.
Journal Contribution
A1
2001
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy
CLAES, Luc
;
Del-Favero, J.
;
Ceulemans, B.
;
Lagae, L.
;
Van Broeckhoven, C.
;
De Jonghe, P.
Journal Contribution
A1