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

B P van de Warrenburg

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Nederlands Tijdschrift Voor Geneeskunde|June 9, 2001
[Autosomal dominant cerebellar ataxias in the Netherlands: a national inventory]B P van de Warrenburg
Nederlands Tijdschrift Voor Geneeskunde|January 13, 2018
[The yips: a movement disorder among golfers]E van Wensen, B P van de Warrenburg
Nederlands Tijdschrift Voor Geneeskunde|April 16, 2004
[From gene to disease; autosomal dominant cerebellar ataxias]H P Kremer, B P van de Warrenburg, R J Sinke
Nederlands Tijdschrift Voor Geneeskunde|November 25, 2003
[A swollen, painless calf caused by neurogenic muscle (pseudo)-hypertrophy]B P van de Warrenburg, M J Zwarts, B G van Engelen
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 15, 2011
The cerebellum in dystonia - help or hindrance?A Sadnicka, B S Hoffland, K P Bhatia, et al.
Clinical Neurology and Neurosurgery|September 24, 1998
The linear naevus sebaceus syndromeB P van de Warrenburg, S van Gulik, W O Renier, et al.
Journal of Neurology|January 14, 2014
GLUT1 deficiency syndrome into adulthood: a follow-up studyW G Leen, M Taher, M M Verbeek, et al.
Brain : a Journal of Neurology|August 13, 2004
Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3D S Verbeek, B P van de Warrenburg, P Wesseling, et al.
Cerebellum (London, England)|September 4, 2014
A gait paradigm reveals different patterns of abnormal cerebellar motor learning in primary focal dystoniasB S Hoffland, L C Veugen, M M H P Janssen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 16, 2012
Marinesco-Sjögren syndrome due to SIL1 mutations with a comment on the clinical phenotypeM Horvers, A K Anttonen, A E Lehesjoki, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Nederlands Tijdschrift Voor Geneeskunde|June 9, 2001
[Autosomal dominant cerebellar ataxias in the Netherlands: a national inventory]B P van de Warrenburg
Nederlands Tijdschrift Voor Geneeskunde|January 13, 2018
[The yips: a movement disorder among golfers]E van Wensen, B P van de Warrenburg
Nederlands Tijdschrift Voor Geneeskunde|April 16, 2004
[From gene to disease; autosomal dominant cerebellar ataxias]H P Kremer, B P van de Warrenburg, R J Sinke
Nederlands Tijdschrift Voor Geneeskunde|November 25, 2003
[A swollen, painless calf caused by neurogenic muscle (pseudo)-hypertrophy]B P van de Warrenburg, M J Zwarts, B G van Engelen
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 15, 2011
The cerebellum in dystonia - help or hindrance?A Sadnicka, B S Hoffland, K P Bhatia, et al.
Clinical Neurology and Neurosurgery|September 24, 1998
The linear naevus sebaceus syndromeB P van de Warrenburg, S van Gulik, W O Renier, et al.
Journal of Neurology|January 14, 2014
GLUT1 deficiency syndrome into adulthood: a follow-up studyW G Leen, M Taher, M M Verbeek, et al.
Brain : a Journal of Neurology|August 13, 2004
Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3D S Verbeek, B P van de Warrenburg, P Wesseling, et al.
Cerebellum (London, England)|September 4, 2014
A gait paradigm reveals different patterns of abnormal cerebellar motor learning in primary focal dystoniasB S Hoffland, L C Veugen, M M H P Janssen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 16, 2012
Marinesco-Sjögren syndrome due to SIL1 mutations with a comment on the clinical phenotypeM Horvers, A K Anttonen, A E Lehesjoki, et al.
Pageof 3