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Neurology
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October 19, 2012
PRRT2 mutation causes benign familial infantile convulsions
Boukje 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 Childhood
P 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 samples
Sarah 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 22q
Petra 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 convulsions
P 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 elastase
P 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 Netherlands
J 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 associated
Deborah 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 study
Martje 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 data
Rianne J M Goselink, Nicol C Voermans, Kees Okkersen, et al.
Page
of 55
Search research articles
Search
Showing results (491-500 of 544) with videos related to
Sort By:
Page
of 55
Neurology
|
October 19, 2012
PRRT2 mutation causes benign familial infantile convulsions
Boukje 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 Childhood
P 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 samples
Sarah 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 22q
Petra 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 convulsions
P 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 elastase
P 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 Netherlands
J 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 associated
Deborah 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 study
Martje 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 data
Rianne J M Goselink, Nicol C Voermans, Kees Okkersen, et al.
Page
of 55