Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M C Y de Wit

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
Neurology|March 2, 2011
Recognizing Guillain-Barre syndrome in preschool childrenJ Roodbol, M C Y de Wit, C Walgaard, et al.
European Journal of Medical Genetics|January 4, 2011
Lung disease in FLNA mutation: confirmatory reportM C Y de Wit, H A W M Tiddens, I F M de Coo, et al.
Neurogenetics|April 23, 2009
Movement disorder and neuronal migration disorder due to ARFGEF2 mutationM C Y de Wit, I F M de Coo, D J J Halley, et al.
Neurology|August 12, 2004
Immediate post-radiotherapy changes in malignant glioma can mimic tumor progressionM C Y de Wit, H G de Bruin, W Eijkenboom, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2009
Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defectsM C Y de Wit, J M Kros, D J J Halley, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 3, 2017
Validated age-specific reference values for CSF total protein levels in childrenV Kahlmann, J Roodbol, N van Leeuwen, et al.
Seizure|July 20, 2010
Absence epilepsy and periventricular nodular heterotopiaM C Y de Wit, H M Schippers, I F M de Coo, et al.
Neurogenetics|September 15, 2006
Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitusM C Y de Wit, I F M de Coo, C Julier, et al.
Journal of Neurology|November 24, 2016
Interdependence of clinical factors predicting cognition in children with tuberous sclerosis complexI E Overwater, B J H Verhaar, H F Lingsma, et al.
Molecular Genetics and Metabolism|November 9, 2005
Brain abnormalities in a case of malonyl-CoA decarboxylase deficiencyM C Y de Wit, I F M de Coo, E Verbeek, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Neurology|March 2, 2011
Recognizing Guillain-Barre syndrome in preschool childrenJ Roodbol, M C Y de Wit, C Walgaard, et al.
European Journal of Medical Genetics|January 4, 2011
Lung disease in FLNA mutation: confirmatory reportM C Y de Wit, H A W M Tiddens, I F M de Coo, et al.
Neurogenetics|April 23, 2009
Movement disorder and neuronal migration disorder due to ARFGEF2 mutationM C Y de Wit, I F M de Coo, D J J Halley, et al.
Neurology|August 12, 2004
Immediate post-radiotherapy changes in malignant glioma can mimic tumor progressionM C Y de Wit, H G de Bruin, W Eijkenboom, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2009
Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defectsM C Y de Wit, J M Kros, D J J Halley, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 3, 2017
Validated age-specific reference values for CSF total protein levels in childrenV Kahlmann, J Roodbol, N van Leeuwen, et al.
Seizure|July 20, 2010
Absence epilepsy and periventricular nodular heterotopiaM C Y de Wit, H M Schippers, I F M de Coo, et al.
Neurogenetics|September 15, 2006
Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitusM C Y de Wit, I F M de Coo, C Julier, et al.
Journal of Neurology|November 24, 2016
Interdependence of clinical factors predicting cognition in children with tuberous sclerosis complexI E Overwater, B J H Verhaar, H F Lingsma, et al.
Molecular Genetics and Metabolism|November 9, 2005
Brain abnormalities in a case of malonyl-CoA decarboxylase deficiencyM C Y de Wit, I F M de Coo, E Verbeek, et al.
Pageof 2