Muscle MRI: a biomarker of disease severity in Duchenne muscular dystrophy? A systematic review

J Ropars, F Gravot, D Ben Salem, F Rousseau… - Neurology, 2020 - AAN Enterprises
Objective To assess the evidence of a relationship between muscle MRI and disease
severity in Duchenne muscular dystrophy (DMD). Methods We conducted a systematic …

The increasing role of muscle MRI to monitor changes over time in untreated and treated muscle diseases

C Nuñez-Peralta, J Alonso-Pérez… - Current Opinion in …, 2020 - journals.lww.com
The latest results obtained from the study of long cohorts of patients with various
neuromuscular diseases open the door to the use of this technology in clinical trials, which …

Utilization of T1-mapping for the pelvic and thigh muscles in Duchenne muscular dystrophy: a quantitative biomarker for disease involvement and correlation with …

F Peng, H Xu, Y Song, K Xu, S Li, X Cai, Y Guo… - BMC Musculoskeletal …, 2022 - Springer
Background Little is known about the disease distribution and severity detected by T1-
mapping in Duchenne muscular dystrophy (DMD). Furthermore, the correlation between …

Quantitative muscle MRI biomarkers in Duchenne muscular dystrophy: cross-sectional correlations with age and functional tests

SP Sherlock, Y Zhang, M Binks… - Biomarkers in …, 2021 - Future Medicine
Aim: Using baseline data from a clinical trial of domagrozumab in Duchenne muscular
dystrophy, we evaluated the correlation between functional measures and quantitative MRI …

Tamoxifen in Duchenne muscular dystrophy (TAMDMD): study protocol for a multicenter, randomized, placebo-controlled, double-blind phase 3 trial

S Nagy, P Hafner, S Schmidt, D Rubino-Nacht… - Trials, 2019 - Springer
Background Duchenne muscular dystrophy (DMD) is an inherited neuromuscular disorder of
childhood with a devastating disease course. Several targeted gene therapies and …

T2 mapping and fat quantification of thigh muscles in children with Duchenne muscular dystrophy

L Yin, Z Xie, H Xu, S Zheng, Z Wang, J Xiao… - Current Medical …, 2019 - Springer
Quantitative magnetic resonance image (MRI) in individual muscles may be useful for
monitoring disease progression in Duchenne muscular dystrophy (DMD). The purpose of …

Using MRI to quantify skeletal muscle pathology in Duchenne muscular dystrophy: A systematic mapping review

L Alic, JF Griffin IV, A Eresen, JN Kornegay… - Muscle & …, 2021 - Wiley Online Library
There is a great demand for accurate non‐invasive measures to better define the natural
history of disease progression or treatment outcome in Duchenne muscular dystrophy …

Quantitative muscle MRI protocol as possible biomarker in Becker muscular dystrophy

L Maggi, M Moscatelli, R Frangiamore, F Mazzi… - Clinical …, 2021 - Springer
Purpose Aim of this study is to compare Quantitative Magnetic Resonance Imaging (qMRI)
measures between Becker Muscular Dystrophy (BMD) and Healthy Subjects (HS) and to …

Intraepineurial fat quantification and cross-sectional area analysis of the sciatic nerve using MRI in Charcot-Marie-Tooth disease type 1A patients

HS Kim, JH Lee, YC Yoon, MJ Cha, SH Nam… - Scientific Reports, 2021 - nature.com
The objectives of this study were to assess the fat fraction (FF) and cross-sectional area
(CSA) of the sciatic nerve in Charcot-Marie-Tooth disease type 1A (CMT1A) patients using …

Longitudinal reliability of outcome measures in patients with Duchenne muscular dystrophy

S Nagy, S Schädelin, P Hafner, U Bonati… - Muscle & …, 2020 - Wiley Online Library
Introduction The definition of reliable outcome measures is of increasing interest in patients
with Duchenne muscular dystrophy (DMD). Methods In this retrospective study, we analyzed …