Related Experiment Video

Updated: Jun 22, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
09:18

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy

Published on: January 12, 2019

Outcome measures in Duchenne muscular dystrophy: are we ready for the new therapeutic era?

Ingemar S J Merkies1, Catharina G Faber

  • 1Department of Neurology, University Hospital Maastricht, P.O. Box 5800, Maastricht, The Netherlands. stapscot@fhcrc.org

Neuromuscular Disorders : NMD
|June 2, 2009
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Assessing Functional Performance in the Mdx Mouse Model
10:32

Assessing Functional Performance in the Mdx Mouse Model

Published on: March 27, 2014

A Simple and Low-cost Assay for Measuring Ambulation in Mouse Models of Muscular Dystrophy
05:54

A Simple and Low-cost Assay for Measuring Ambulation in Mouse Models of Muscular Dystrophy

Published on: December 29, 2017

Related Experiment Videos

Last Updated: Jun 22, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
09:18

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy

Published on: January 12, 2019

Assessing Functional Performance in the Mdx Mouse Model
10:32

Assessing Functional Performance in the Mdx Mouse Model

Published on: March 27, 2014

A Simple and Low-cost Assay for Measuring Ambulation in Mouse Models of Muscular Dystrophy
05:54

A Simple and Low-cost Assay for Measuring Ambulation in Mouse Models of Muscular Dystrophy

Published on: December 29, 2017

Related Concept Videos

Satellite Stem Cells and Muscular Dystrophy01:21

Satellite Stem Cells and Muscular Dystrophy

Satellite stem cells or myosatellite cells are quiescent stem cells that Alexander Mauro first identified in 1961. These cells are located between the sarcolemma, the plasma membrane of muscle fibers, and the basal lamina, the connective tissue sheath covering it. These mononucleated cells are activated in response to muscle injury, can transform into myoblasts, and may form or repair muscle fibers. Myosatellite cells can provide additional myonuclei for muscle regeneration or return to a...

Articles linked to this work by shared authors, journal, and citation graph.

Annual assessment of ECG intervals in patients with myotonic dystrophy type 1 using a mobile 6‑lead ECG device: TeleCheck-DM1.

International journal of cardiology. Heart & vasculature·2026

The Burden of Small Fiber Neuropathy: Changes in Pain, Costs, and Quality of Life Before and After Diagnosis.

Journal of the peripheral nervous system : JPNS·2026

Energy expenditure and the accuracy of predictive equations in myotonic dystrophy type 1.

Journal of neuromuscular diseases·2026

Rasch-Built Overall Disability Scale for Chronic Idiopathic Axonal Polyneuropathy.

Neurology·2026

Clinical impact of medication reconciliation on physicians' treatment policies at outpatient clinics: a cross-sectional study.

BMC health services research·2026

Polyneuropathy in kidney transplant recipients: a cross-sectional study in Groningen, the Netherlands.

BMJ open·2026

Validation of non-instrumental clinical outcome assessments for dysphagia in OPMD: A structured, COSMIN-guided assessment.

Neuromuscular disorders : NMD·2026

Juvenile dermatomyositis across diagnostic eras: treatment evolution and long-term outcomes in a 25-year cohort.

Neuromuscular disorders : NMD·2026

A late-onset slowly progressive dystrophic-myasthenic phenotype expands the clinical spectrum of TOR1AIP1-related disease.

Neuromuscular disorders : NMD·2026

Generalized edema as the initial manifestation of Anti-TIF1γ-positive dermatomyositis associated with ovarian cancer.

Neuromuscular disorders : NMD·2026

Development of Italian centile curves for the North Star Ambulatory Assessment and timed items.

Neuromuscular disorders : NMD·2026

Interindividual variability of muscle involvement on imaging in a family with FLNC c.577G>A (p.A193T)-related myopathy.

Neuromuscular disorders : NMD·2026
See all related articles
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
Jove
Visualize
Contact Us