Introduction: The main objective of this study was to describe muscle involvement on whole-body magnetic resonance imaging scans in adults at different stages of glycogen-storage disease type III (GSDIII). Methods: Fifteen patients, 16–59 years of age, were examined on a 3-T system. The examinations consisted of coronal and axial T1-weighted images or fat images with a Dixon technique, and were scored for 47 muscles using Mercuri's classification. Muscle changes consisted of internal bright signals of fatty replacement. Results: Distribution across muscles showed predominant signal alteration in the lower limbs and postural muscles. This finding is consistent with the overall clinical presentation of GSDIII and the results of heatmap scores...
Contains fulltext : 81766.pdf (publisher's version ) (Closed access)The purpose of...
Background: Limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) is a progressive myopathy caus...
peer reviewedBACKGROUND AND OBJECTIVE: To identify the most responsive and sensitive clinical outcom...
Debranching enzyme deficiency (Glycogen storage disease (GSD) type III) causes progressive muscle wa...
PURPOSE: To evaluate differences in diffusion parameters in thigh muscles in patients with glycogen ...
Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and charact...
PURPOSE: The continuous discovery of new subtypes of neuromuscular disorders demands more accurate ...
BACKGROUND Limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) is a progressive myopathy ca...
Contains fulltext : 137803.pdf (publisher's version ) (Open Access)Facioscapulohum...
Background: Lipid storage myopathy (LSM) is a genetically heterogeneous group with variable clinical...
The role of neuromuscular imaging in the diagnosis of inherited and acquired muscle diseases has gai...
Although it has been shown that muscle magnetic resonance imaging (MRI) improves the phenotypic char...
We conducted a prospective multinational study of muscle pathology using magnetic resonance imaging ...
Objective: The aim of the study was to evaluate whether the visual analysis of muscle magnetic reson...
This study describes muscle involvement on whole-body MRI (WB-MRI) scans at different stages of McAr...
Contains fulltext : 81766.pdf (publisher's version ) (Closed access)The purpose of...
Background: Limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) is a progressive myopathy caus...
peer reviewedBACKGROUND AND OBJECTIVE: To identify the most responsive and sensitive clinical outcom...
Debranching enzyme deficiency (Glycogen storage disease (GSD) type III) causes progressive muscle wa...
PURPOSE: To evaluate differences in diffusion parameters in thigh muscles in patients with glycogen ...
Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and charact...
PURPOSE: The continuous discovery of new subtypes of neuromuscular disorders demands more accurate ...
BACKGROUND Limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) is a progressive myopathy ca...
Contains fulltext : 137803.pdf (publisher's version ) (Open Access)Facioscapulohum...
Background: Lipid storage myopathy (LSM) is a genetically heterogeneous group with variable clinical...
The role of neuromuscular imaging in the diagnosis of inherited and acquired muscle diseases has gai...
Although it has been shown that muscle magnetic resonance imaging (MRI) improves the phenotypic char...
We conducted a prospective multinational study of muscle pathology using magnetic resonance imaging ...
Objective: The aim of the study was to evaluate whether the visual analysis of muscle magnetic reson...
This study describes muscle involvement on whole-body MRI (WB-MRI) scans at different stages of McAr...
Contains fulltext : 81766.pdf (publisher's version ) (Closed access)The purpose of...
Background: Limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A) is a progressive myopathy caus...
peer reviewedBACKGROUND AND OBJECTIVE: To identify the most responsive and sensitive clinical outcom...