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

Wim H J P Linssen

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 31, 2009
The cognitive profile of amyotrophic lateral sclerosis: A meta-analysisJoost Raaphorst, Marianne de Visser, Wim H J P Linssen, et al.
Neuromuscular Disorders : NMD|September 2, 2014
Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophiesLeroy Ten Dam, Anneke J van der Kooi, Fleur Rövekamp, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 25, 2010
[Amyotrophic lateral sclerosis and frontotemporal dementia: overlapping characteristics]Joost Raaphorst, Hepke F Grupstra, Wim H J P Linssen, et al.
Archives of Neurology|January 21, 2004
Polymyositis: an ongoing discussion about a disease entityIrene M Bronner, Wim H J P Linssen, Marjon F G van der Meulen, et al.
Parkinsonism & Related Disorders|April 3, 2012
Paroxysmal kinesigenic dyskinesia: cortical or non-cortical originTeun W van Strien, Anne-Fleur van Rootselaar, Anthony A J Hilgevoord, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Cognitive dysfunction in lower motor neuron disease: executive and memory deficits in progressive muscular atrophyJoost Raaphorst, Marianne de Visser, Marie-José van Tol, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 13, 2007
Sumatriptan nasal spray in the acute treatment of migraine in adolescents and childrenPetra M C Callenbach, Lise P M Pels, Paul G H Mulder, et al.
American Journal of Human Genetics|January 26, 2010
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophiesVéronique Bolduc, Gareth Marlow, Kym M Boycott, et al.
Neurology|September 14, 2012
The ALS-FTD-Q: a new screening tool for behavioral disturbances in ALSJoost Raaphorst, Emma Beeldman, Ben Schmand, et al.
Clinical Genetics|March 29, 2019
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patientsLeroy Ten Dam, Wendy S Frankhuizen, Wim H J P Linssen, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 31, 2009
The cognitive profile of amyotrophic lateral sclerosis: A meta-analysisJoost Raaphorst, Marianne de Visser, Wim H J P Linssen, et al.
Neuromuscular Disorders : NMD|September 2, 2014
Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophiesLeroy Ten Dam, Anneke J van der Kooi, Fleur Rövekamp, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 25, 2010
[Amyotrophic lateral sclerosis and frontotemporal dementia: overlapping characteristics]Joost Raaphorst, Hepke F Grupstra, Wim H J P Linssen, et al.
Archives of Neurology|January 21, 2004
Polymyositis: an ongoing discussion about a disease entityIrene M Bronner, Wim H J P Linssen, Marjon F G van der Meulen, et al.
Parkinsonism & Related Disorders|April 3, 2012
Paroxysmal kinesigenic dyskinesia: cortical or non-cortical originTeun W van Strien, Anne-Fleur van Rootselaar, Anthony A J Hilgevoord, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Cognitive dysfunction in lower motor neuron disease: executive and memory deficits in progressive muscular atrophyJoost Raaphorst, Marianne de Visser, Marie-José van Tol, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 13, 2007
Sumatriptan nasal spray in the acute treatment of migraine in adolescents and childrenPetra M C Callenbach, Lise P M Pels, Paul G H Mulder, et al.
American Journal of Human Genetics|January 26, 2010
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophiesVéronique Bolduc, Gareth Marlow, Kym M Boycott, et al.
Neurology|September 14, 2012
The ALS-FTD-Q: a new screening tool for behavioral disturbances in ALSJoost Raaphorst, Emma Beeldman, Ben Schmand, et al.
Clinical Genetics|March 29, 2019
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patientsLeroy Ten Dam, Wendy S Frankhuizen, Wim H J P Linssen, et al.
Pageof 2