Review of upper extremity passive joint impedance identification in people with Duchenne Muscular Dystrophy
Abstract Duchenne Muscular Dystrophy (DMD) progressively leads to loss of limb function due to muscle weakness. The incurable nature of the disease shifts the focus to improving quality of life, including assistive supports to improve arm function. Over time, the passive joint impedance (Jimp) of pe...
Saved in:
Main Authors: | Suzanne J. Filius, Kyriacos Papa, Jaap Harlaar |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2025-01-01
|
Series: | Journal of NeuroEngineering and Rehabilitation |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12984-024-01537-0 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A structural genomics approach to investigate Dystrophin mutations and their impact on the molecular pathways of Duchenne muscular dystrophy
by: Abdelbaset Mohamed Elasbali, et al.
Published: (2025-02-01) -
Unraveling the Genetic Heartbeat: Decoding Cardiac Involvement in Duchenne Muscular Dystrophy
by: Valeria Novelli, et al.
Published: (2025-01-01) -
Pharmacological interventions for the management of anesthesia and sedation in patients with Duchenne muscular dystrophy: a systematic review and meta-analysis
by: Xianghong Lian, et al.
Published: (2025-01-01) -
Titin fragment is a sensitive biomarker in Duchenne muscular dystrophy model mice carrying full-length human dystrophin gene on human artificial chromosome
by: Yosuke Hiramuki, et al.
Published: (2025-01-01) -
Co-occurrence of CAPN3 homozygous mutation and CCTG expansion
in the CNBP gene in a patient
with muscular dystrophy
by: Wiktoria Radziwonik-Frączyk, et al.
Published: (2024-07-01)