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

Henry Houlden

Showing results (1-10 of 934) with videos related to

Pageof 94
Sort By:
Brain : a Journal of Neurology|February 26, 2013
Defective N-linked protein glycosylation pathway in congenital myasthenic syndromesHenry Houlden
Journal of Human Genetics|July 13, 2012
A Commentary on 'Four novel C20ORF54 mutations identified in Brown-Vialetto-Van Laere syndrome patients.'Henry Houlden
Neurology|April 15, 2009
The small, spastic, and furrowed tongue of Allgrove syndromeHenry Houlden
Journal of Neurology, Neurosurgery, and Psychiatry|August 2, 2012
Sniffing out the cerebellumHenry Houlden
Brain : a Journal of Neurology|February 21, 2012
Extending the clinical spectrum of pain channelopathiesHenry Houlden
Current Neurology and Neuroscience Reports|April 25, 2012
Recent advances in the genetics of cerebellar ataxiasAnna Sailer, Henry Houlden
Neurology|March 21, 2014
Defects of RNA metabolism in the pathogenesis of spinal muscular atrophyEnrico Bertini, Henry Houlden
Journal of Neurology, Neurosurgery, and Psychiatry|February 16, 2026
Heterozygous variants in <i>SLC12A6</i> should be considered in all cases of suspected inherited neuropathyNatalia Domink, Henry Houlden
Handbook of Clinical Neurology|September 25, 2024
White matter disorders with cerebral calcification in adulthoodViorica Chelban, Henry Houlden
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 28, 2020
Genetic epilepsies and the K<sub>v</sub> super-familyVincenzo Salpietro, Henry Houlden
Pageof 94

Showing results (1-10 of 934) with videos related to

Sort By:
Pageof 94
Brain : a Journal of Neurology|February 26, 2013
Defective N-linked protein glycosylation pathway in congenital myasthenic syndromesHenry Houlden
Journal of Human Genetics|July 13, 2012
A Commentary on 'Four novel C20ORF54 mutations identified in Brown-Vialetto-Van Laere syndrome patients.'Henry Houlden
Neurology|April 15, 2009
The small, spastic, and furrowed tongue of Allgrove syndromeHenry Houlden
Journal of Neurology, Neurosurgery, and Psychiatry|August 2, 2012
Sniffing out the cerebellumHenry Houlden
Brain : a Journal of Neurology|February 21, 2012
Extending the clinical spectrum of pain channelopathiesHenry Houlden
Current Neurology and Neuroscience Reports|April 25, 2012
Recent advances in the genetics of cerebellar ataxiasAnna Sailer, Henry Houlden
Neurology|March 21, 2014
Defects of RNA metabolism in the pathogenesis of spinal muscular atrophyEnrico Bertini, Henry Houlden
Journal of Neurology, Neurosurgery, and Psychiatry|February 16, 2026
Heterozygous variants in <i>SLC12A6</i> should be considered in all cases of suspected inherited neuropathyNatalia Domink, Henry Houlden
Handbook of Clinical Neurology|September 25, 2024
White matter disorders with cerebral calcification in adulthoodViorica Chelban, Henry Houlden
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 28, 2020
Genetic epilepsies and the K<sub>v</sub> super-familyVincenzo Salpietro, Henry Houlden
Pageof 94