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Helene Verhelst

Showing results (11-20 of 41) with videos related to

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BMC Medical Genetics|May 4, 2017
Severe congenital microcephaly with AP4M1 mutation, a case reportSarah Duerinckx, Helene Verhelst, Camille Perazzolo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 8, 2016
Multiple sclerosis in Belgian children: A multicentre retrospective studyHelene Verhelst, Liesbeth De Waele, Nicolas Deconinck, et al.
Current Pediatric Reviews|June 27, 2025
The Relationship Between Hypotonia and Vestibular Dysfunction in Young Children: A Scoping ReviewLena Van den Bossche, Leen Maes, Frederic Acke, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 10, 2010
Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA clusterHelene Verhelst, Patrick Verloo, Karlien Dhondt, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 12, 2018
Recurrent arterial ischemic stroke with good response to mycophenolate mofetilBenedikte Van Driessche, Patrick Verloo, Nele Herregods, et al.
The International Journal of Artificial Organs|October 10, 2015
Therapeutic plasma exchange in children with acute autoimmune central nervous system disordersAgnieszka Prytuła, Johan Vande Walle, Helene Verhelst, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 28, 2014
Lambert-Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplicationSabine Verbeek, Olivier Vanakker, Rudy Mercelis, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|December 5, 2024
Seizure quantification in sunflower syndrome by a wrist-worn deviceJo Sourbron, Renee Proost, Jan Vandenneucker, et al.
Electrophoresis|October 29, 2009
Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNAJoél Smet, Sara Seneca, Boel De Paepe, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 13, 2013
Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature reviewIbrahim Tanyalçin, Helene Verhelst, Dicky J J Halley, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
BMC Medical Genetics|May 4, 2017
Severe congenital microcephaly with AP4M1 mutation, a case reportSarah Duerinckx, Helene Verhelst, Camille Perazzolo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 8, 2016
Multiple sclerosis in Belgian children: A multicentre retrospective studyHelene Verhelst, Liesbeth De Waele, Nicolas Deconinck, et al.
Current Pediatric Reviews|June 27, 2025
The Relationship Between Hypotonia and Vestibular Dysfunction in Young Children: A Scoping ReviewLena Van den Bossche, Leen Maes, Frederic Acke, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 10, 2010
Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA clusterHelene Verhelst, Patrick Verloo, Karlien Dhondt, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 12, 2018
Recurrent arterial ischemic stroke with good response to mycophenolate mofetilBenedikte Van Driessche, Patrick Verloo, Nele Herregods, et al.
The International Journal of Artificial Organs|October 10, 2015
Therapeutic plasma exchange in children with acute autoimmune central nervous system disordersAgnieszka Prytuła, Johan Vande Walle, Helene Verhelst, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 28, 2014
Lambert-Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplicationSabine Verbeek, Olivier Vanakker, Rudy Mercelis, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|December 5, 2024
Seizure quantification in sunflower syndrome by a wrist-worn deviceJo Sourbron, Renee Proost, Jan Vandenneucker, et al.
Electrophoresis|October 29, 2009
Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNAJoél Smet, Sara Seneca, Boel De Paepe, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 13, 2013
Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature reviewIbrahim Tanyalçin, Helene Verhelst, Dicky J J Halley, et al.
Pageof 5