Add to ORKGDermatomyositis was diagnosed on clinical and muscle histological criteria in a 42-year-old woman. Despite treatment, the patient complained of deterioration of her muscle condition. Since her symptoms were discordant with the rest of the data, muscle biopsy was performed and disclosed rod-bearing non-atrophic fibers as the unique and predominant pathological feature. Their significance is examined in this paper
Dermatomyositis (DM) is an idiopathic inflammatory myopathy characterized by the presence of skin le...
OBJECTIVE: To study muscle biopsies, using histochemistry, on ten children with infantile dermatomyo...
Dermatomyositis (DM) is a rare connective corresponding to an inflammatory disease of skeletal muscl...
International audienceDermatomyositis was diagnosed on clinical and muscle histological criteria in ...
Objective: To report pathologic findings in 124 Australian and North American cases of primary nemal...
BACKGROUND: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, cha...
Nemaline myopathies are a heterogenous group of congenital myopathies caused by de novo, dominantly ...
Objective: This study aims to investigate the clinical manifestations and muscular pathological chan...
International audienceNemaline myopathy (NM) is a rare congenital myopathy characterised by hypotoni...
Nemaline rod myopathy (NM) is a rare form of congenital myopathy characterized by slowly progressive...
BackgroundSporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, chara...
The nemaline myopathies constitute a large proportion of the congenital or structural myopathies. Co...
Nemaline myopathy is a structural congenital myopathy associated with the presence of rodlike struct...
Sporadic late-onset nemaline myopathy (SLONM) is a rare acquired myopathy characterized by rapid-ons...
BACKGROUND: Dermatomyositis affects striated muscles, skin and other organs. OBJECTIVE: To charact...
Dermatomyositis (DM) is an idiopathic inflammatory myopathy characterized by the presence of skin le...
OBJECTIVE: To study muscle biopsies, using histochemistry, on ten children with infantile dermatomyo...
Dermatomyositis (DM) is a rare connective corresponding to an inflammatory disease of skeletal muscl...
International audienceDermatomyositis was diagnosed on clinical and muscle histological criteria in ...
Objective: To report pathologic findings in 124 Australian and North American cases of primary nemal...
BACKGROUND: Sporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, cha...
Nemaline myopathies are a heterogenous group of congenital myopathies caused by de novo, dominantly ...
Objective: This study aims to investigate the clinical manifestations and muscular pathological chan...
International audienceNemaline myopathy (NM) is a rare congenital myopathy characterised by hypotoni...
Nemaline rod myopathy (NM) is a rare form of congenital myopathy characterized by slowly progressive...
BackgroundSporadic late-onset nemaline myopathy (SLONM) is a rare, late-onset muscle disorder, chara...
The nemaline myopathies constitute a large proportion of the congenital or structural myopathies. Co...
Nemaline myopathy is a structural congenital myopathy associated with the presence of rodlike struct...
Sporadic late-onset nemaline myopathy (SLONM) is a rare acquired myopathy characterized by rapid-ons...
BACKGROUND: Dermatomyositis affects striated muscles, skin and other organs. OBJECTIVE: To charact...
Dermatomyositis (DM) is an idiopathic inflammatory myopathy characterized by the presence of skin le...
OBJECTIVE: To study muscle biopsies, using histochemistry, on ten children with infantile dermatomyo...
Dermatomyositis (DM) is a rare connective corresponding to an inflammatory disease of skeletal muscl...