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Pediatric Neurology|September 12, 2012
Contribution of the corticospinal tract to motor impairment in spina bifidaNiels Geerdink, Inge Cuppen, Jan Rotteveel, et al.
Developmental Medicine and Child Neurology|August 30, 2008
Compound muscle action potentials in newborn infants with spina bifidaNiels Geerdink, Jaco W Pasman, Jan J Rotteveel, et al.
Pediatric Neurology|February 7, 2006
Responses to lumbar magnetic stimulation in newborns with spina bifidaNiels Geerdink, Jaco W Pasman, Nel Roeleveld, et al.
International Journal of Molecular Sciences|July 14, 2023
An E280K Missense Variant in KCND3/Kv4.3-Case Report and Functional CharacterizationRichard Ågren, Niels Geerdink, Han G Brunner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 7, 2012
Motor evoked potentials and compound muscle action potentials as prognostic tools for neonates with spina bifidaInge Cuppen, Niels Geerdink, Jan J Rotteveel, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 2, 2012
Essential features of Chiari II malformation in MR imaging: an interobserver reliability study--part 1Niels Geerdink, Ton van der Vliet, Jan J Rotteveel, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 8, 2012
Interobserver reliability and diagnostic performance of Chiari II malformation measures in MR imaging--part 2Niels Geerdink, Ton van der Vliet, Jan J Rotteveel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 29, 2008
PMTS and stress response sequences in parents of children with spina bifidaIgnace P R Vermaes, Jan R M Gerris, Reinier A Mullaart, et al.
Fetal Diagnosis and Therapy|November 18, 2014
Small biparietal diameter and head circumference are part of the phenotype instead of independent prognostic markers in fetuses with spinal dysraphismInge Cuppen, Dagmar de Bruijn, Niels Geerdink, et al.
European Journal of Human Genetics : EJHG|October 16, 2003
MECP2 analysis in mentally retarded patients: implications for routine DNA diagnosticsTjitske Kleefstra, Helger G Yntema, Willy M Nillesen, et al.
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