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

Sithara Ramdas

Showing results (21-30 of 49) with videos related to

Pageof 5
Sort By:
Wellcome Open Research|June 10, 2020
Sodium channel myotonia may be associated with high-risk brief resolved unexplained eventsGabriel Cea, Daniel Andreu, Elaine Fletcher, et al.
Pediatric Neurology|June 14, 2023
Care Recommendations for the Investigation and Management of Children With Skeletal Muscle ChannelopathiesEmma Matthews, Jacqueline Palace, Sithara Ramdas, et al.
BMJ Neurology Open|April 3, 2025
Epidemiology and 10-year clinical care of juvenile myasthenia gravis in England: a retrospective cohort studyAli Abbasi, Kerina Bonar, Piotr Zaremba, et al.
Expert Opinion on Therapeutic Targets|December 16, 2022
Early clinical and pre-clinical therapy development in Nemaline myopathyGemma Fisher, Laurane Mackels, Theodora Markati, et al.
Brain Communications|November 30, 2023
Congenital myasthenic syndromes: a retrospective natural history study of respiratory outcomes in a single centreJordan Poulos, Martin Samuels, Jacqueline Palace, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 25, 2020
Prevalence and incidence of neuromyelitis optica spectrum disorder, aquaporin-4 antibody-positive NMOSD and MOG antibody-positive disease in Oxfordshire, UKKaren O'Connell, Antonia Hamilton-Shield, Mark Woodhall, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 27, 2021
Isolated central nervous system familial hemophagocytic lymphohistiocytosis (fHLH) presenting as a mimic of demyelination in childrenAmitav Parida, Omar Abdel-Mannan, Kshitij Mankad, et al.
Developmental Medicine and Child Neurology|January 11, 2023
Antineurofascin IgG2-associated paediatric autoimmune nodopathyRachel E Harris, Mark Atherton, Johann Te Water Naude, et al.
Practical Neurology|December 15, 2022
Muscle cramps and contractures: causes and treatmentJildou N Dijkstra, Eline Boon, Nick Kruijt, et al.
Muscle & Nerve|November 18, 2025
Prevalence and Geographical Distribution of Patients With Congenital Myasthenic Syndromes in the United KingdomElena Rossini, Leighann Henehan, Yin Yao Dong, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Wellcome Open Research|June 10, 2020
Sodium channel myotonia may be associated with high-risk brief resolved unexplained eventsGabriel Cea, Daniel Andreu, Elaine Fletcher, et al.
Pediatric Neurology|June 14, 2023
Care Recommendations for the Investigation and Management of Children With Skeletal Muscle ChannelopathiesEmma Matthews, Jacqueline Palace, Sithara Ramdas, et al.
BMJ Neurology Open|April 3, 2025
Epidemiology and 10-year clinical care of juvenile myasthenia gravis in England: a retrospective cohort studyAli Abbasi, Kerina Bonar, Piotr Zaremba, et al.
Expert Opinion on Therapeutic Targets|December 16, 2022
Early clinical and pre-clinical therapy development in Nemaline myopathyGemma Fisher, Laurane Mackels, Theodora Markati, et al.
Brain Communications|November 30, 2023
Congenital myasthenic syndromes: a retrospective natural history study of respiratory outcomes in a single centreJordan Poulos, Martin Samuels, Jacqueline Palace, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 25, 2020
Prevalence and incidence of neuromyelitis optica spectrum disorder, aquaporin-4 antibody-positive NMOSD and MOG antibody-positive disease in Oxfordshire, UKKaren O'Connell, Antonia Hamilton-Shield, Mark Woodhall, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 27, 2021
Isolated central nervous system familial hemophagocytic lymphohistiocytosis (fHLH) presenting as a mimic of demyelination in childrenAmitav Parida, Omar Abdel-Mannan, Kshitij Mankad, et al.
Developmental Medicine and Child Neurology|January 11, 2023
Antineurofascin IgG2-associated paediatric autoimmune nodopathyRachel E Harris, Mark Atherton, Johann Te Water Naude, et al.
Practical Neurology|December 15, 2022
Muscle cramps and contractures: causes and treatmentJildou N Dijkstra, Eline Boon, Nick Kruijt, et al.
Muscle & Nerve|November 18, 2025
Prevalence and Geographical Distribution of Patients With Congenital Myasthenic Syndromes in the United KingdomElena Rossini, Leighann Henehan, Yin Yao Dong, et al.
Pageof 5