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

Nicholas E Johnson

Showing results (61-70 of 110) with videos related to

Pageof 11
Sort By:
Neurology|June 17, 2016
Disease burden and functional outcomes in congenital myotonic dystrophy: A cross-sectional studyNicholas E Johnson, Russell Butterfield, Kiera Berggren, et al.
Developmental Medicine and Child Neurology|October 30, 2015
Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophyNicholas E Johnson, Anne-Berit Ekstrom, Craig Campbell, et al.
Developmental Medicine and Child Neurology|September 4, 2024
Parental diagnostic delay and developmental outcomes in congenital and childhood-onset myotonic dystrophy type 1Federica Trucco, Emilio Albamonte, Marika Pane, 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.
Muscle & Nerve|July 13, 2019
Patient-reported study of the impact of pediatric-onset myotonic dystrophyMichael Hunter, Anne-Berit Ekstrom, Craig Campbell, et al.
Journal of Multidisciplinary Healthcare|October 21, 2016
Same-day physical therapy consults in an outpatient neuromuscular disease physician clinicEvan M Pucillo, Nancy Christensen-Mayer, Shelly D Poole, et al.
Neuromuscular Disorders : NMD|December 28, 2021
Patient reported quality of life in limb girdle muscular dystrophyLaurel V Kovalchick, Kameron Bates, Jeffrey Statland, 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.
Journal of the Peripheral Nervous System : JPNS|June 9, 2020
Validation of the Italian version of the Charcot-Marie-Tooth Health IndexChiara Pisciotta, Emma Ciafaloni, Riccardo Zuccarino, et al.
Neurology. Clinical Practice|November 22, 2019
Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1Nicholas E Johnson, Eugenio Zapata Aldana, Nathalie Angeard, et al.
Pageof 11

Showing results (61-70 of 110) with videos related to

Sort By:
Pageof 11
Neurology|June 17, 2016
Disease burden and functional outcomes in congenital myotonic dystrophy: A cross-sectional studyNicholas E Johnson, Russell Butterfield, Kiera Berggren, et al.
Developmental Medicine and Child Neurology|October 30, 2015
Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophyNicholas E Johnson, Anne-Berit Ekstrom, Craig Campbell, et al.
Developmental Medicine and Child Neurology|September 4, 2024
Parental diagnostic delay and developmental outcomes in congenital and childhood-onset myotonic dystrophy type 1Federica Trucco, Emilio Albamonte, Marika Pane, 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.
Muscle & Nerve|July 13, 2019
Patient-reported study of the impact of pediatric-onset myotonic dystrophyMichael Hunter, Anne-Berit Ekstrom, Craig Campbell, et al.
Journal of Multidisciplinary Healthcare|October 21, 2016
Same-day physical therapy consults in an outpatient neuromuscular disease physician clinicEvan M Pucillo, Nancy Christensen-Mayer, Shelly D Poole, et al.
Neuromuscular Disorders : NMD|December 28, 2021
Patient reported quality of life in limb girdle muscular dystrophyLaurel V Kovalchick, Kameron Bates, Jeffrey Statland, 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.
Journal of the Peripheral Nervous System : JPNS|June 9, 2020
Validation of the Italian version of the Charcot-Marie-Tooth Health IndexChiara Pisciotta, Emma Ciafaloni, Riccardo Zuccarino, et al.
Neurology. Clinical Practice|November 22, 2019
Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1Nicholas E Johnson, Eugenio Zapata Aldana, Nathalie Angeard, et al.
Pageof 11