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Showing results (491-500 of 544) with videos related to

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Neurology|October 19, 2012
PRRT2 mutation causes benign familial infantile convulsionsBoukje de Vries, Petra M C Callenbach, Jessica T Kamphorst, 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.
International Journal of Cardiology|April 22, 2020
A morphology based deep learning model for atrial fibrillation detection using single cycle electrocardiographic samplesSarah W E Baalman, Florian E Schroevers, Abel J Oakley, et al.
Epilepsia|September 27, 2003
Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22qPetra M C Callenbach, Arn M J M van den Maagdenberg, Jouke J Hottenga, 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.
The Journal of Rheumatology|February 1, 1994
Early cartilage degradation in cationic immune complex arthritis in mice: relative role of interleukin 1, the polymorphonuclear cell (PMN) and PMN elastaseP L van Lent, A E van den Hoek, L A van den Bersselaar, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 6, 2013
Impact of introduction of mid-trimester scan on pregnancy outcome of open spina bifida in The NetherlandsJ H Fleurke-Rozema, T A Vogel, B J Voskamp, et al.
Developmental Medicine and Child Neurology|May 18, 2011
In children with Friedreich ataxia, muscle and ataxia parameters are associatedDeborah A Sival, Maria E Pouwels, Agnes Van Brederode, et al.
Orphanet Journal of Rare Diseases|March 8, 2017
The efficacy of the modified Atkins diet in North Sea Progressive Myoclonus Epilepsy: an observational prospective open-label studyMartje E van Egmond, Amerins Weijenberg, Margreet E van Rijn, et al.
Neuromuscular Disorders : NMD|November 6, 2017
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient dataRianne J M Goselink, Nicol C Voermans, Kees Okkersen, et al.
Pageof 55

Showing results (491-500 of 544) with videos related to

Sort By:
Pageof 55
Neurology|October 19, 2012
PRRT2 mutation causes benign familial infantile convulsionsBoukje de Vries, Petra M C Callenbach, Jessica T Kamphorst, 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.
International Journal of Cardiology|April 22, 2020
A morphology based deep learning model for atrial fibrillation detection using single cycle electrocardiographic samplesSarah W E Baalman, Florian E Schroevers, Abel J Oakley, et al.
Epilepsia|September 27, 2003
Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22qPetra M C Callenbach, Arn M J M van den Maagdenberg, Jouke J Hottenga, 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.
The Journal of Rheumatology|February 1, 1994
Early cartilage degradation in cationic immune complex arthritis in mice: relative role of interleukin 1, the polymorphonuclear cell (PMN) and PMN elastaseP L van Lent, A E van den Hoek, L A van den Bersselaar, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 6, 2013
Impact of introduction of mid-trimester scan on pregnancy outcome of open spina bifida in The NetherlandsJ H Fleurke-Rozema, T A Vogel, B J Voskamp, et al.
Developmental Medicine and Child Neurology|May 18, 2011
In children with Friedreich ataxia, muscle and ataxia parameters are associatedDeborah A Sival, Maria E Pouwels, Agnes Van Brederode, et al.
Orphanet Journal of Rare Diseases|March 8, 2017
The efficacy of the modified Atkins diet in North Sea Progressive Myoclonus Epilepsy: an observational prospective open-label studyMartje E van Egmond, Amerins Weijenberg, Margreet E van Rijn, et al.
Neuromuscular Disorders : NMD|November 6, 2017
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient dataRianne J M Goselink, Nicol C Voermans, Kees Okkersen, et al.
Pageof 55