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

Cheryl Longman

Showing results (21-30 of 57) with videos related to

Pageof 6
Sort By:
Neuromuscular Disorders : NMD|October 7, 2022
Masseter muscle volume as a disease marker in adult-onset myotonic dystrophy type 1Agata Oliwa, Clarissa Hocking, Mark J Hamilton, et al.
Frontiers in Neurology|October 19, 2018
Outcome Measures for Central Nervous System Evaluation in Myotonic Dystrophy Type 1 May Be Confounded by Deficits in Motor Function or InsightMark J Hamilton, John McLean, Sarah Cumming, et al.
Neuromuscular Disorders : NMD|August 27, 2025
Selective muscle MRI changes in a patient with a rare mitochondrial DNA variant causing myoclonic epilepsy with ragged red fibresTaylor Watson-Fargie, David G Anderson, William Stewart, et al.
Neuromuscular Disorders : NMD|July 3, 2021
The phenotypic and genotypic features of a Scottish cohort with McArdle diseaseSacha E Gandhi, Cheryl Longman, Richard K H Petty, et al.
Neuromuscular Disorders : NMD|August 19, 2023
Glycogen storage disease type IV without detectable polyglucosan bodies: importance of broad gene panelsAgata Oliwa, Gavin Langlands, Anna Sarkozy, et al.
Human Molecular Genetics|September 11, 2003
Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycanCheryl Longman, Martin Brockington, Silvia Torelli, et al.
Acta Neuropathologica|April 12, 2013
Recessive desmin-null muscular dystrophy with central nuclei and mitochondrial abnormalitiesMatthew Henderson, Liesbeth De Waele, Judith Hudson, et al.
Neuromuscular Disorders : NMD|December 18, 2003
A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycanPervin Dinçer, Burcu Balci, Yeliz Yuva, et al.
Clinical Rehabilitation|November 19, 2013
A multicentre postal survey investigating the contribution of illness perceptions, coping and optimism to quality of life and mood in adults with muscle diseaseChristopher D Graham, John Weinman, Reza Sadjadi, et al.
Archives of Neurology|January 16, 2008
Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variantEmma M Clement, Caroline Godfrey, Jenny Tan, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Neuromuscular Disorders : NMD|October 7, 2022
Masseter muscle volume as a disease marker in adult-onset myotonic dystrophy type 1Agata Oliwa, Clarissa Hocking, Mark J Hamilton, et al.
Frontiers in Neurology|October 19, 2018
Outcome Measures for Central Nervous System Evaluation in Myotonic Dystrophy Type 1 May Be Confounded by Deficits in Motor Function or InsightMark J Hamilton, John McLean, Sarah Cumming, et al.
Neuromuscular Disorders : NMD|August 27, 2025
Selective muscle MRI changes in a patient with a rare mitochondrial DNA variant causing myoclonic epilepsy with ragged red fibresTaylor Watson-Fargie, David G Anderson, William Stewart, et al.
Neuromuscular Disorders : NMD|July 3, 2021
The phenotypic and genotypic features of a Scottish cohort with McArdle diseaseSacha E Gandhi, Cheryl Longman, Richard K H Petty, et al.
Neuromuscular Disorders : NMD|August 19, 2023
Glycogen storage disease type IV without detectable polyglucosan bodies: importance of broad gene panelsAgata Oliwa, Gavin Langlands, Anna Sarkozy, et al.
Human Molecular Genetics|September 11, 2003
Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycanCheryl Longman, Martin Brockington, Silvia Torelli, et al.
Acta Neuropathologica|April 12, 2013
Recessive desmin-null muscular dystrophy with central nuclei and mitochondrial abnormalitiesMatthew Henderson, Liesbeth De Waele, Judith Hudson, et al.
Neuromuscular Disorders : NMD|December 18, 2003
A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycanPervin Dinçer, Burcu Balci, Yeliz Yuva, et al.
Clinical Rehabilitation|November 19, 2013
A multicentre postal survey investigating the contribution of illness perceptions, coping and optimism to quality of life and mood in adults with muscle diseaseChristopher D Graham, John Weinman, Reza Sadjadi, et al.
Archives of Neurology|January 16, 2008
Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variantEmma M Clement, Caroline Godfrey, Jenny Tan, et al.
Pageof 6