Results 211 to 220 of about 1,587,143 (318)
Muscle fibre type shift in COPD: Adaptive, maladaptive or a bit of both?
Experimental Physiology, EarlyView.
Jacob Peter Hartmann +2 more
wiley +1 more source
ABSTRACT Objective This study aimed to determine the outcomes of patients that have refractory anti‐melanoma differentiation‐associated gene 5 (MDA5) antibody‐positive clinically amyopathic dermatomyositis with rapidly progressive interstitial pneumonia treated with tacrolimus trough concentration‐escalating bipartite therapy (glucocorticoids combined ...
Anji Xiong +10 more
wiley +1 more source
Recent advances in immunological mechanisms and murine disease models of idiopathic inflammatory myopathies. [PDF]
Nishidate A +3 more
europepmc +1 more source
Chimeric Antigen Receptor T‐Cell Therapy and Autoimmune Diseases in the Nervous System
ABSTRACT Introduction Chimeric antigen receptor T‐cell (CAR‐T) therapy, a revolutionary immunotherapy originally developed for hematologic malignancies, has recently gained attention for its potential in treating autoimmune diseases. Increasing evidence suggests that CAR‐T cells can precisely target pathogenic immune populations, offering durable ...
Shun‐yu Yao +11 more
wiley +1 more source
The changed transcriptome of muscular dystrophy and inflammatory myopathy : contributions of non-coding RNAs to muscle damage and recovery [PDF]
De Paepe, Boel
core +1 more source
THU0365 INCREASED HSP90 IN MUSCLE TISSUE AND PLASMA ASSOCIATES WITH DISEASE ACTIVITY AND SKELETAL MUSCLE INVOLVEMENT IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES [PDF]
Hana Štorkánová +11 more
openalex +1 more source
ABSTRACT Meningiomas (MGMs) are the most prevalent benign intracranial tumors in adults, with incidence markedly increasing with age, underscoring the need to explore aging‐associated molecular mechanisms. In this study, we integrated transcriptomic datasets (GSE43290, GSE54934, GSE77259, and GSE183655) from the GEO database and aging‐related genes ...
Guangyu Du +7 more
wiley +1 more source
ABSTRACT Phosphomannomutase deficiency (PMM2‐CDG) is the most common congenital disorder of glycosylation, characterized by variable early‐onset neurological (hypotonia, cerebellar syndrome, developmental delay) and multi‐organ manifestations. Although several clinical trials are ongoing, current biomarkers lack prognostic or monitoring utility ...
Florencia Epifani +14 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

