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

Emma Matthews

Showing results (11-20 of 71) with videos related to

Pageof 8
Sort By:
Lancet (London, England)|June 11, 2019
Genotype-phenotype association in patients with SCN4A mutation - Authors' replyEmma Matthews, Roope Männikkö, Elijah Behr, et al.
Neurologic Clinics|July 25, 2020
Skeletal Muscle ChannelopathiesVinojini Vivekanandam, Pinki Munot, Michael G Hanna, et al.
Expert Review of Molecular Diagnostics|July 14, 2020
Improving genetic diagnostics of skeletal muscle channelopathiesVinojini Vivekanandam, Roope Männikkö, Emma Matthews, et al.
The Lancet. Child & Adolescent Health|March 7, 2020
Muscle and brain sodium channelopathies: genetic causes, clinical phenotypes, and management approachesEmma Matthews, Simona Balestrini, Sanjay M Sisodiya, et al.
The Lancet. Child & Adolescent Health|May 7, 2022
Accelerating the genetic diagnosis of neurological disorders presenting with episodic apnoea in infancyBryony Silksmith, Pinki Munot, Luke Starling, et al.
The Cochrane Database of Systematic Reviews|May 6, 2016
Corticosteroids for the treatment of Duchenne muscular dystrophyEmma Matthews, Ruth Brassington, Thierry Kuntzer, et al.
Archives of Neurology|January 12, 2011
Stridor as a neonatal presentation of skeletal muscle sodium channelopathyEmma Matthews, Adnan Y Manzur, Richa Sud, et al.
Zeitschrift Fur Evidenz, Fortbildung Und Qualitat Im Gesundheitswesen|June 23, 2023
Insights into Advance Care Planning in AfricaDianah Basirika, Anne Merriman, Nelson Gumoyesige, et al.
Journal of Human Genetics|February 19, 2024
Leigh syndrome with developmental regression and ataxia due to a novel splicing variant in the PMPCB geneEmma Matthews, Ella F Whittle, Faraan Khan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2018
Acetazolamide can improve symptoms and signs in ion channel-related congenital myopathyEmma Matthews, Louise Hartley, Richa Sud, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
Lancet (London, England)|June 11, 2019
Genotype-phenotype association in patients with SCN4A mutation - Authors' replyEmma Matthews, Roope Männikkö, Elijah Behr, et al.
Neurologic Clinics|July 25, 2020
Skeletal Muscle ChannelopathiesVinojini Vivekanandam, Pinki Munot, Michael G Hanna, et al.
Expert Review of Molecular Diagnostics|July 14, 2020
Improving genetic diagnostics of skeletal muscle channelopathiesVinojini Vivekanandam, Roope Männikkö, Emma Matthews, et al.
The Lancet. Child & Adolescent Health|March 7, 2020
Muscle and brain sodium channelopathies: genetic causes, clinical phenotypes, and management approachesEmma Matthews, Simona Balestrini, Sanjay M Sisodiya, et al.
The Lancet. Child & Adolescent Health|May 7, 2022
Accelerating the genetic diagnosis of neurological disorders presenting with episodic apnoea in infancyBryony Silksmith, Pinki Munot, Luke Starling, et al.
The Cochrane Database of Systematic Reviews|May 6, 2016
Corticosteroids for the treatment of Duchenne muscular dystrophyEmma Matthews, Ruth Brassington, Thierry Kuntzer, et al.
Archives of Neurology|January 12, 2011
Stridor as a neonatal presentation of skeletal muscle sodium channelopathyEmma Matthews, Adnan Y Manzur, Richa Sud, et al.
Zeitschrift Fur Evidenz, Fortbildung Und Qualitat Im Gesundheitswesen|June 23, 2023
Insights into Advance Care Planning in AfricaDianah Basirika, Anne Merriman, Nelson Gumoyesige, et al.
Journal of Human Genetics|February 19, 2024
Leigh syndrome with developmental regression and ataxia due to a novel splicing variant in the PMPCB geneEmma Matthews, Ella F Whittle, Faraan Khan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2018
Acetazolamide can improve symptoms and signs in ion channel-related congenital myopathyEmma Matthews, Louise Hartley, Richa Sud, et al.
Pageof 8