Sporadic inclusion-body myositis(s-IBM) is a rare muscle disease in Asia population.The main clinical symptoms are characterized by a chronic progressive muscle weakness in the limbs after 50 yeas old.Muscle biopsy showed usually rimmed vacuoles in muscle fibers,angular atrophicSporadic inclusion-body myositis(s-IBM) is a rare muscle disease in Asia population.The main clinical symptoms are characterized by a chronic progressive muscle weakness in the limbs after 50 yeas old.Muscle biopsy showed usually rimmed vacuoles in muscle fibers,angular atrophic中华医学会、中华医学会神经病学分会
Myopathy is a typical clinical finding among patients with the 3243A>G mutation in mitochondrial ...
Mitochondrial disorders (MDs) are inherited multi-organ diseases with variable phenotypes. Inclusion...
Muscle mass and function are gradually lost in age-related, degenerative neuromuscular disorders, wh...
The sporadic form of inclusion body myositis (IBM) is the most common late-onset myopathy. Its compl...
The sporadic form of inclusion body myositis (IBM) is the most common late-onset myopathy. Its compl...
Sporadic inclusion body myositis (sIBM) is a late onset disorder of unkown aetiology. Mitochondrial ...
Abstract Sporadic inclusion body myositis (IBM) is the most common idiopathic inflammatory myopathy ...
OBJECTIVE: The current pathological diagnostic criteria for sporadic inclusion body myositis (IBM) l...
Sporadic inclusion body myositis (IBM) is the commonest acquired myopathy in individuals aged over 5...
Sporadic inclusion body myositis (sIBM) is one of the most common myopathies in elderly people. Mito...
Sporadic inclusion-body myositis (s-IBM) usually presents after the age of 40 years and is the most ...
Inclusion body myositis (IBM) is an autoimmune, inflammatory myopathy where morphological changes of...
Sporadic inclusion body myositis (sIBM) is considered to be the most common acquired muscle disease ...
Sporadic inclusion-body myositis (IBM) is the most common myopathy in individuals over 55 years of a...
Inclusion body myositis (IBM) is a slowly progressive muscle disease affecting ageing individuals. I...
Myopathy is a typical clinical finding among patients with the 3243A>G mutation in mitochondrial ...
Mitochondrial disorders (MDs) are inherited multi-organ diseases with variable phenotypes. Inclusion...
Muscle mass and function are gradually lost in age-related, degenerative neuromuscular disorders, wh...
The sporadic form of inclusion body myositis (IBM) is the most common late-onset myopathy. Its compl...
The sporadic form of inclusion body myositis (IBM) is the most common late-onset myopathy. Its compl...
Sporadic inclusion body myositis (sIBM) is a late onset disorder of unkown aetiology. Mitochondrial ...
Abstract Sporadic inclusion body myositis (IBM) is the most common idiopathic inflammatory myopathy ...
OBJECTIVE: The current pathological diagnostic criteria for sporadic inclusion body myositis (IBM) l...
Sporadic inclusion body myositis (IBM) is the commonest acquired myopathy in individuals aged over 5...
Sporadic inclusion body myositis (sIBM) is one of the most common myopathies in elderly people. Mito...
Sporadic inclusion-body myositis (s-IBM) usually presents after the age of 40 years and is the most ...
Inclusion body myositis (IBM) is an autoimmune, inflammatory myopathy where morphological changes of...
Sporadic inclusion body myositis (sIBM) is considered to be the most common acquired muscle disease ...
Sporadic inclusion-body myositis (IBM) is the most common myopathy in individuals over 55 years of a...
Inclusion body myositis (IBM) is a slowly progressive muscle disease affecting ageing individuals. I...
Myopathy is a typical clinical finding among patients with the 3243A>G mutation in mitochondrial ...
Mitochondrial disorders (MDs) are inherited multi-organ diseases with variable phenotypes. Inclusion...
Muscle mass and function are gradually lost in age-related, degenerative neuromuscular disorders, wh...