Results 251 to 260 of about 1,622,130 (371)
ABSTRACT Background The diagnosis of inclusion body myositis (IBM) can be delayed because of its heterogeneous clinical presentation and the lack of specific biomarkers. Muscle imaging has gained increasing relevance over the past decade and is now included among the supportive criteria in the international diagnostic guidelines.
Eleonora Torchia +15 more
wiley +1 more source
Cardiovascular risk and lipid-lowering therapy in idiopathic inflammatory myopathies: a call for improved, disease-specific risk assessment. [PDF]
Loh K, Rose E, Tansley S.
europepmc +1 more source
Rituximab in Patients with Inflammatory Myopathies [PDF]
Seong Wook Kang
openalex +1 more source
ABSTRACT Background Low muscle oxidative capacity is an extrapulmonary manifestation of chronic obstructive pulmonary disease (COPD) with unclear aetiology. We sought to characterize locomotor muscle oxidative capacity in never smokers and ever smokers with and without COPD and determine clinical and behavioural features associated with low muscle ...
Alessandra Adami +5 more
wiley +1 more source
Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies. [PDF]
Luo YB +8 more
europepmc +1 more source
ABSTRACT Background Duchenne muscular dystrophy (DMD) is a severe, life‐limiting neuromuscular disorder (NMD) characterized by progressive muscle wasting and mitochondrial dysfunction. Although gene therapies offer promise, even those already approved by regulatory agencies, their use remains constrained by mutation specificity, delivery challenges and
Sean Y. Ng +12 more
wiley +1 more source
Immunoadsorption as a novel therapy for refractory idiopathic inflammatory myopathies: a retrospective observational study. [PDF]
Kastrati K +13 more
europepmc +1 more source
Associated Factors for the Occurrence of Rapidly Progressive Interstitial Lung Disease in Patients with Idiopathic Inflammatory Myopathies: A Systematic Review and Meta-analysis [PDF]
Weiwei Yuan +5 more
openalex +1 more source
ABSTRACT Background Skeletal muscle wasting and weakness are prominent disease features. Originally considered to arise from common transcriptional changes, recent analyses demonstrated that different stimuli induce muscle wasting via largely distinct mRNA and protein changes.
Anna Stephan +6 more
wiley +1 more source

