L. Claes

发表

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.

L. Lagae, C. Broeckhoven, C. van Broeckhoven, 2001, American journal of human genetics.

De novo KCNQ2 mutations in patients with benign neonatal seizures

C. van Broeckhoven, K. Claeys, B. Ceulemans, 2004, Neurology.

Four generations of epilepsy caused by an inherited microdeletion of the SCN1A gene

A. Suls, P. de Jonghe, A. Jordanova, 2010, Neurology.

A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy

C. van Broeckhoven, B. Ceulemans, P. de Jonghe, 2003, Neurology.

A novel GABRG2 mutation associated with febrile seizures

L. Lagae, C. van Broeckhoven, K. Claeys, 2006, Neurology.

Differential diagnosis of neurologically expressed disorders in Western European cattle.

E. Thiry, C. Saegerman, S. Roels, 2003, Revue scientifique et technique.

A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus

Dyck, W. van Paesschen, C. van Broeckhoven, 2005, Journal of Medical Genetics.

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

W. van Paesschen, C. van Broeckhoven, C. Depondt, 2004, Journal of Medical Genetics.

Trichinella infection in wild boars and synanthropic rats in northwest Vietnam.

N. Praet, P. Dorny, S. Gabriël, 2014, Veterinary parasitology.

Seroprevalence of trichinellosis in domestic animals in northwestern Vietnam.

N. Praet, P. Dorny, S. Gabriël, 2013, Veterinary parasitology.

Population-Level Retrospective Study of Neurologically Expressed Disorders in Ruminants before the Onset of Bovine Spongiform Encephalopathy (BSE) in Belgium, a BSE Risk III Country

E. Thiry, C. Saegerman, S. Roels, 2005, Journal of Clinical Microbiology.