Rhe rigid spine syndrome in two sistersVANNESTE, J. A. L; AUGUSTIJN, P. B; STAM, F. C et al.Journal of neurology, neurosurgery and psychiatry. 1988, Vol 51, Num 1, pp 131-135, issn 0022-3050Article

High Prevalence of Short-Chain Acyl-CoA Dehydrogenase Deficiency in the Netherlands, but No Association with Epilepsy of Unknown Origin in ChildhoodVAN MALDEGEM, B. T; KLOOSTERMAN, S. F; JANSSEN, W. J et al.Neuropediatrics. 2011, Vol 42, Num 1, pp 13-17, issn 0174-304X, 5 p.Article

Ring chromosome 20 epilepsy syndrome in children: Electroclinical featuresAUGUSTIJN, P. B; PARRA, J; WOUTERS, C. H et al.Neurology. 2001, Vol 57, Num 6, pp 1108-1111, issn 0028-3878Article

A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (epm2)SERRATOSA, J. M; GOMEZ-GARREL, P; TOPCU, M et al.Human molecular genetics (Print). 1999, Vol 8, Num 2, pp 345-352, issn 0964-6906Article

A special case of congenital adrenal hypoplasia and acute bilateral infantile striatal necrosisVAN DER ENT, C. K; DE VROEDE, M. A. M. J; AUGUSTIJN, P. B et al.Acta paediatrica (Oslo). 1995, Vol 84, Num 8, pp 957-960, issn 0803-5253Article