Severe early onset osteopenia and osteoporosis caused by antiepileptic drugsBEERHORST, K; HUVERS, F. C; RENIER, W. O et al.Netherlands journal of medicine. 2005, Vol 63, Num 6, pp 222-226, issn 0300-2977, 5 p.Article

Generalized convulsive status epilepticus : causes, therapy, and outcome in 346 patientsSCHOLTES, F. B; RENIER, W. O; MEINARDI, H et al.Epilepsia (Copenhagen). 1994, Vol 35, Num 5, pp 1104-1112, issn 0013-9580Article

Non-convulsive status epilepticus : causes, treatment, and outcome in 65 patientsSCHOLTES, F. B; RENIER, W. O; MEINARDI, H et al.Journal of neurology, neurosurgery and psychiatry. 1996, Vol 61, Num 1, pp 93-95, issn 0022-3050Article

Simple partial status epilepticus : causes, treatment, and outcome in 47 patientsSCHOLTES, F. B; RENIER, W. O; MEINARDI, H et al.Journal of neurology, neurosurgery and psychiatry. 1996, Vol 61, Num 1, pp 90-92, issn 0022-3050Article

Moya-Moya syndrome and primary pulmonary hypertension in childhoodKAPUSTA, L; DANIELS, O; RENIER, W. O et al.Neuropediatrics. 1990, Vol 21, Num 3, pp 162-163, issn 0174-304X, 2 p.Article

Intellectual sequelae of primary non-obstructive hydrocephalus in infancy: analysis of 50 casesHEIJ, O; RENIER, W. O; GABREELS, F. J. M et al.Clinical neurology and neurosurgery. 1985, Vol 87, Num 4, pp 247-253, issn 0303-8467Article

Diagnostic reference frames for seizures : A validation studyVAN AST, J. F; RENIER, W. O; TALMON, J. L et al.Journal of neurology. 2006, Vol 253, Num 3, pp 372-376, issn 0340-5354, 5 p.Article

Development and developmental disorders of the human cerebellumTEN DONKELAAR, H. J; LAMMENS, M; WESSELING, P et al.Journal of neurology. 2003, Vol 250, Num 9, pp 1025-1036, issn 0340-5354, 12 p.Article

Polyglucosan bodies in brain tissue: a systematic studyBUSARD, H. L. S. M; SPAN, J. P. T; RENKAWEK, K et al.Clinical neuropathology. 1994, Vol 13, Num 2, pp 60-63, issn 0722-5091Conference Paper

Hereditary neuropathy with liability to pressure palsies in childhoodGABREËLS-FESTEN, A. A. W. M; GABREËLS, F. J. M; JOOSTEN, E. M. G et al.Neuropediatrics. 1992, Vol 23, Num 3, pp 138-143, issn 0174-304XArticle

Subacute sclerosing panencephalitis in the Netherlands 1976-1990BEERSMA, M. F. C; GALAMA, J. M. D; VAN DRUTEN, H. A. M et al.International journal of epidemiology. 1992, Vol 21, Num 3, pp 583-588, issn 0300-5771Article

Congenital muscular dystrophy with eye and brain malformations in six dutch patientsLEYTEN, Q. H; GABREËLS, F. J. M; RENIER, W. O et al.Neuropediatrics. 1992, Vol 23, Num 6, pp 316-320, issn 0174-304XArticle

Neuropathological findings in muscle-eye-brain disease (MEB-D) : neuropathological delineation of MEB-D from congenital muscular dystrophy of the Fukuyama typeLEYTEN, Q. H; RENKAWEK, K; RENIER, W. O et al.Acta neuropathologica. 1991, Vol 83, Num 1, pp 55-60, issn 0001-6322Article

Polyglucosan bodies in intramuscular motor nervesBERNSEN, R. A. J. A. M; BUSARD, H. L. S. M; TER LAAK, H. J et al.Acta neuropathologica. 1989, Vol 77, Num 6, pp 629-633, issn 0001-6322Article

Morphological and biochemical analysis of a brain biopsy in a case of idiopathic Lennox-Gastaut syndromeRENIER, W. O; GABREELS, F. J. M; JASPAR, H. H. J et al.Epilepsia (Copenhagen). 1988, Vol 29, Num 5, pp 644-649, issn 0013-9580Article

Chronic inflammatory demyelinating polyneuropathy in two siblingsGABREELS-FESTEN, A. A. W. M; HAGEMAN, A. T. M; GABREELS, F. J. M et al.Journal of neurology, neurosurgery and psychiatry. 1986, Vol 49, Num 2, pp 152-156, issn 0022-3050Article

Neurophysiological studies in the Leigh syndromeVAN ERVEN, P. M; COLON, E. J; GABREELS, F. J et al.Brain & development (Tokyo. 1979). 1986, Vol 8, Num 6, pp 590-595, issn 0387-7604Article

Generalized hypertrophic myopathy associated with chorioretinal dystrophy and struma lymphomatosa ― A case reportVAN ZUILLEN, E. V; GABREELS, F. J. M; RENIER, W. O et al.Neuropediatrics. 1984, Vol 15, Num 3, pp 159-164, issn 0174-304XArticle

Calcium-phosphate metabolism in autosomal recessive idiopathic strio-pallidodentate calcinosis and Cockayne's syndromeSMITS, M. G; GABREELS, F. J. M; FROELING, P. G. A et al.Clinical neurology and neurosurgery. 1983, Vol 85, Num 3, pp 145-153, issn 0303-8467Article

Can determination of lactic acid and pyruvic acid in cerebrospinal fluid help in diagnosing central nervous system involvement in systemic lupus erythematosus?DUINKERKE, S. J; GABREELS, F. J. M; BOERBOOMS, A. M. T et al.Clinical neurology and neurosurgery. 1983, Vol 85, Num 4, pp 225-230, issn 0303-8467Article

Drug load in clinical trials : A neglected factorDECKERS, C. L. P; HEKSTER, Y. A; KEYSER, A et al.Clinical pharmacology and therapeutics. 1997, Vol 62, Num 6, pp 592-595, issn 0009-9236Article

Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosisJOHNSON, J. L; RAJAGOPALAN, K. V; RENIER, W. O et al.Prenatal diagnosis. 2002, Vol 22, Num 5, pp 433-436, issn 0197-3851Article

Long-term treatment retention with topiramate. Authors' replyDECKERS, C. L. P; RENIER, W. O; LHATOO, S. D et al.Epilepsia (Copenhagen). 2001, Vol 42, Num 2, pp 290-291, issn 0013-9580Article

Angelman syndrome without detectable chromosome 15q11-13 anomaly : Clinical study of familial and isolated casesLAAN, L. A. E. M; HALLEY, D. J. J; DEN BOER, A. T et al.American journal of medical genetics. 1998, Vol 76, Num 3, pp 262-268, issn 0148-7299Article

Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expressionVERHAGEN, W. I. M; BARTELS, R. H. A. M; FRANSEN, E et al.Journal of the neurological sciences. 1998, Vol 158, Num 1, pp 101-105, issn 0022-510XArticle