P De Jonghe

Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies

J. Meuleman, K. Venken, V. Timmerman, 2001, Neuroreport.

Mutations in GDAP1

C. van Broeckhoven, F. Palau, V. Timmerman, 2002, Neurology.

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.

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

I. Scheffer, L. Lagae, S. Berkovic, 2010, Neurology.

Familial occipitotemporal lobe epilepsy and migraine with visual aura

W. van Paesschen, K. Claeys, W. Paesschen, 2007, Neurology.