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O F Brouwer

Showing results (101-110 of 114) with videos related to

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Early Human Development|September 25, 2009
Neurophysiological evaluation in children with Friedreich's ataxiaD A Sival, G J du Marchie Sarvaas, O F Brouwer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 27, 2004
Interrater agreement of the diagnosis and classification of a first seizure in childhood. The Dutch Study of Epilepsy in ChildhoodH Stroink, C A van Donselaar, A T Geerts, et al.
American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, et al.
Epilepsia|February 1, 1997
Evolution of epilepsy and EEG findings in Angelman syndromeL A Laan, W O Renier, W F Arts, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|February 15, 2003
Neurophysiological analysis of leg movements in infants with spina bifida aperta in the early postnatal periodD A Sival, T W van Weerden, W F A den Dunnen, et al.
Journal of Medical Genetics|May 1, 1992
Oculoauriculovertebral spectrum and cerebral anomaliesC T Schrander-Stumpel, C E de Die-Smulders, R C Hennekam, et al.
Clinical Genetics|March 19, 2010
A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrumJ Van Reeuwijk, M J W Olderode-Berends, C Van den Elzen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 28, 2017
Spasticity, dyskinesia and ataxia in cerebral palsy: Are we sure we can differentiate them?H Eggink, D Kremer, O F Brouwer, et al.
Clinical and Experimental Immunology|March 26, 2003
Immunoglobulins in children with epilepsy: the Dutch Study of Epilepsy in ChildhoodP M C Callenbach, C M Jol-Van Der Zijde, A T Geerts, et al.
Clinical Genetics|April 29, 2005
Refinement of the chromosome 16 locus for benign familial infantile convulsionsP M C Callenbach, E H van den Boogerd, R F M de Coo, et al.
Pageof 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
Early Human Development|September 25, 2009
Neurophysiological evaluation in children with Friedreich's ataxiaD A Sival, G J du Marchie Sarvaas, O F Brouwer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 27, 2004
Interrater agreement of the diagnosis and classification of a first seizure in childhood. The Dutch Study of Epilepsy in ChildhoodH Stroink, C A van Donselaar, A T Geerts, et al.
American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, et al.
Epilepsia|February 1, 1997
Evolution of epilepsy and EEG findings in Angelman syndromeL A Laan, W O Renier, W F Arts, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|February 15, 2003
Neurophysiological analysis of leg movements in infants with spina bifida aperta in the early postnatal periodD A Sival, T W van Weerden, W F A den Dunnen, et al.
Journal of Medical Genetics|May 1, 1992
Oculoauriculovertebral spectrum and cerebral anomaliesC T Schrander-Stumpel, C E de Die-Smulders, R C Hennekam, et al.
Clinical Genetics|March 19, 2010
A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrumJ Van Reeuwijk, M J W Olderode-Berends, C Van den Elzen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 28, 2017
Spasticity, dyskinesia and ataxia in cerebral palsy: Are we sure we can differentiate them?H Eggink, D Kremer, O F Brouwer, et al.
Clinical and Experimental Immunology|March 26, 2003
Immunoglobulins in children with epilepsy: the Dutch Study of Epilepsy in ChildhoodP M C Callenbach, C M Jol-Van Der Zijde, A T Geerts, et al.
Clinical Genetics|April 29, 2005
Refinement of the chromosome 16 locus for benign familial infantile convulsionsP M C Callenbach, E H van den Boogerd, R F M de Coo, et al.
Pageof 12