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 …

[HTML][HTML] MR imaging of inherited myopathies: a review and proposal of imaging algorithms

LU Aivazoglou, JB Guimarães, TM Link, MAF Costa… - European …, 2021 - Springer
Purpose of review The aims of this review are to discuss the imaging modalities used to
assess muscle changes in myopathies, to provide an overview of the inherited myopathies …

Deep learning-based thigh muscle segmentation for reproducible fat fraction quantification using fat–water decomposition MRI

J Ding, P Cao, HC Chang, Y Gao, SHS Chan… - Insights into …, 2020 - Springer
Background Time-efficient and accurate whole volume thigh muscle segmentation is a major
challenge in moving from qualitative assessment of thigh muscle MRI to more quantitative …

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 …

Clinical utilisation of multimodal quantitative magnetic resonance imaging in investigating muscular damage in Duchenne muscular dystrophy: a study on the …

Y Song, H Xu, K Xu, Y Guo, L Xie, F Peng, R Xu… - Pediatric …, 2023 - Springer
Background Duchenne muscular dystrophy (DMD) is a neuromuscular disease
characterised by progressive muscular weakness and atrophy. Currently, studies on DMD …

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 Multi‐Parametric Quantitative Magnetic Resonance Imaging in the Early Diagnosis of Duchenne Muscular Dystrophy

F Peng, D Tang, W Qing, W Chen, S Li… - Journal of Magnetic …, 2023 - Wiley Online Library
Background It is challenging to diagnose suspected Duchenne muscular dystrophy (DMD)
patients in the very early stage of the disease. More evidence is needed to demonstrate the …

[HTML][HTML] Longitudinal study of multi-parameter quantitative magnetic resonance imaging in Duchenne muscular dystrophy: hyperresponsiveness of gluteus maximus …

F Peng, H Xu, Y Song, K Xu, S Li, X Cai, Y Guo… - Journal of …, 2023 - Springer
Objective To describe the disease progression of Duchenne muscular dystrophy (DMD) in
the pelvic and thigh muscles over 1-year using multiple-parameter quantitative magnetic …

Quantitative muscle analysis in FSHD using whole-body fat-referenced MRI: composite scores for longitudinal and cross-sectional analysis

ML Mellion, P Widholm, M Karlsson, A Ahlgren… - Neurology, 2022 - AAN Enterprises
Background and Objectives Facioscapulohumeral muscular dystrophy (FSHD) is a rare,
debilitating disease characterized by progressive muscle weakness. MRI is a sensitive …

Orthogonal proteomics methods warrant the development of Duchenne muscular dystrophy biomarkers

C Johansson, H Hunt, M Signorelli, F Edfors, A Hober… - Clinical Proteomics, 2023 - Springer
Background Molecular components in blood, such as proteins, are used as biomarkers to
detect or predict disease states, guide clinical interventions and aid in the development of …