Background: Collagen VI-related myopathies are autosomal dominant and recessive hereditary myopathies, mainly including Ullrich congenital muscular dystrophy (UCMD) and Bethlem myopathy (BM). Muscle magnetic resonance imaging (MRI) has been widely used to diagnosis muscular disorders. The purpose of this study was to evaluate the diagnostic value of thigh muscles MRI for collagen VI-related myopathies. Methods: Eleven patients with collagen VI gene mutation-related myopathies were enrolled in this study. MRI of the thigh muscles was performed in all patients with collagen VI gene mutation-related myopathies and in 361 patients with other neuromuscular disorders (disease controls). T1-weighted images were used to assess fatty infiltration of...
BackgroundThe diagnosis of patients with mutations in the VCP gene can be complicated due to their b...
The classical phenotypes of collagen VI-associated myopathies are well described. Little is known, h...
International audienceBackground: Dominant and recessive autosomal pathogenic variants in the three ...
Background: Collagen VI-related myopathies are autosomal dominant and recessive hereditary myopathie...
Bethlem myopathy and Ullrich congenital muscular dystrophy are part of the heterogeneous group of co...
The aim of this study was to evaluate muscle magnetic resonance imaging findings in patients with co...
Ullrich congenital muscular dystrophy (UCMD) is a genetically and clinically heterogeneous muscle di...
The aim of this study was to evaluate muscle magnetic resonance imaging findings in patients with co...
INTRODUCTION: Collagen VI expression was tested in peripheral blood macrophages from patients with ...
Introduction: Collagen VI expression was tested in peripheral blood macrophages from patients with c...
BACKGROUND AND PURPOSE: Mutations in collagen VI-related genes (COL6A1, COL6A2, and COL6A3) cause Be...
International audienceABSTRACT: Collagen VI-myopathies, caused by mutations in the genes encoding co...
Ullrich congenital muscular dystrophy (UCMD) is clinically characterized by muscle weakness, proxima...
Mutations in human collagen VI genes cause a spectrum of musculoskeletal conditions in children and ...
Ullrich congenital muscular dystrophy (UCMD) is clinically characterized by muscle weakness, proxima...
BackgroundThe diagnosis of patients with mutations in the VCP gene can be complicated due to their b...
The classical phenotypes of collagen VI-associated myopathies are well described. Little is known, h...
International audienceBackground: Dominant and recessive autosomal pathogenic variants in the three ...
Background: Collagen VI-related myopathies are autosomal dominant and recessive hereditary myopathie...
Bethlem myopathy and Ullrich congenital muscular dystrophy are part of the heterogeneous group of co...
The aim of this study was to evaluate muscle magnetic resonance imaging findings in patients with co...
Ullrich congenital muscular dystrophy (UCMD) is a genetically and clinically heterogeneous muscle di...
The aim of this study was to evaluate muscle magnetic resonance imaging findings in patients with co...
INTRODUCTION: Collagen VI expression was tested in peripheral blood macrophages from patients with ...
Introduction: Collagen VI expression was tested in peripheral blood macrophages from patients with c...
BACKGROUND AND PURPOSE: Mutations in collagen VI-related genes (COL6A1, COL6A2, and COL6A3) cause Be...
International audienceABSTRACT: Collagen VI-myopathies, caused by mutations in the genes encoding co...
Ullrich congenital muscular dystrophy (UCMD) is clinically characterized by muscle weakness, proxima...
Mutations in human collagen VI genes cause a spectrum of musculoskeletal conditions in children and ...
Ullrich congenital muscular dystrophy (UCMD) is clinically characterized by muscle weakness, proxima...
BackgroundThe diagnosis of patients with mutations in the VCP gene can be complicated due to their b...
The classical phenotypes of collagen VI-associated myopathies are well described. Little is known, h...
International audienceBackground: Dominant and recessive autosomal pathogenic variants in the three ...