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

Katherine D Mathews

Showing results (51-60 of 125) with videos related to

Pageof 13
Sort By:
Neuromuscular Disorders : NMD|May 16, 2018
Uniparental disomy unveils a novel recessive mutation in POMT2Brianna N Brun, Tobias Willer, Benjamin W Darbro, et al.
Muscle & Nerve|November 17, 2021
A population-based study of scoliosis among males diagnosed with a dystrophinopathy identified by the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet)Kristin M Conway, Amber Gedlinske, Katherine D Mathews, et al.
Neurology|August 9, 2020
Motor outcome measures in patients with <i>FKRP</i> mutations: A longitudinal follow-upAmber M Gedlinske, Carrie M Stephan, Shelley R H Mockler, et al.
BMC Neurology|March 16, 2024
Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD studyAmy Doody, Lindsay Alfano, Jordi Diaz-Manera, et al.
Annals of Clinical and Translational Neurology|April 17, 2025
UDP-glucose dehydrogenase variants cause dystroglycanopathyAnna M Reelfs, Carrie M Stephan, Theresa M Czech, et al.
Journal of the Neurological Sciences|June 10, 2011
Mortality in Friedreich ataxiaAmy Y Tsou, Erin K Paulsen, Sarah J Lagedrost, et al.
Neuromuscular Disorders : NMD|May 21, 2022
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research NetworkPangaja Paramsothy, Yinding Wang, Bo Cai, et al.
Muscle & Nerve|March 21, 2022
Time to diagnosis of Duchenne muscular dystrophy remains unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000-2015Shiny Thomas, Kristin M Conway, Olushola Fapo, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 22, 2010
Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathyRobert M Weiss, Richard E Kerber, Jane K Jones, et al.
Journal of Child Neurology|September 7, 2010
Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophyKatherine D Mathews, Chris Cunniff, Jiji R Kantamneni, et al.
Pageof 13

Showing results (51-60 of 125) with videos related to

Sort By:
Pageof 13
Neuromuscular Disorders : NMD|May 16, 2018
Uniparental disomy unveils a novel recessive mutation in POMT2Brianna N Brun, Tobias Willer, Benjamin W Darbro, et al.
Muscle & Nerve|November 17, 2021
A population-based study of scoliosis among males diagnosed with a dystrophinopathy identified by the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet)Kristin M Conway, Amber Gedlinske, Katherine D Mathews, et al.
Neurology|August 9, 2020
Motor outcome measures in patients with <i>FKRP</i> mutations: A longitudinal follow-upAmber M Gedlinske, Carrie M Stephan, Shelley R H Mockler, et al.
BMC Neurology|March 16, 2024
Defining clinical endpoints in limb girdle muscular dystrophy: a GRASP-LGMD studyAmy Doody, Lindsay Alfano, Jordi Diaz-Manera, et al.
Annals of Clinical and Translational Neurology|April 17, 2025
UDP-glucose dehydrogenase variants cause dystroglycanopathyAnna M Reelfs, Carrie M Stephan, Theresa M Czech, et al.
Journal of the Neurological Sciences|June 10, 2011
Mortality in Friedreich ataxiaAmy Y Tsou, Erin K Paulsen, Sarah J Lagedrost, et al.
Neuromuscular Disorders : NMD|May 21, 2022
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research NetworkPangaja Paramsothy, Yinding Wang, Bo Cai, et al.
Muscle & Nerve|March 21, 2022
Time to diagnosis of Duchenne muscular dystrophy remains unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000-2015Shiny Thomas, Kristin M Conway, Olushola Fapo, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 22, 2010
Exercise-induced left ventricular systolic dysfunction in women heterozygous for dystrophinopathyRobert M Weiss, Richard E Kerber, Jane K Jones, et al.
Journal of Child Neurology|September 7, 2010
Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophyKatherine D Mathews, Chris Cunniff, Jiji R Kantamneni, et al.
Pageof 13