Disease: Idiopathic myopathy
- A novel grey scale and Power Doppler ultrasonographic score for idiopathic inflammatory myopathies: Siena Myositis Ultrasound Grading Scale
- A Novel Presentation of Refractory Immune Thrombocytopenia in Anti-synthetase Syndrome: A Case Report
- Activation of TLR4 induces inflammatory muscle injury via mTOR and NF-κB pathways in experimental autoimmune myositis mice
- An epidemiological investigation of an idiopathic myopathy in hunting dogs in New Zealand
- Anti-Ro52/Anti-nuclear Matrix Protein 2 Positive Clinically Amyopathic Dermatomyositis Presented Only With Interstitial Lung Disease
- Association between self-reported race and ethnicity and myositis-specific autoantibodies in a diverse cohort of patients with inflammatory myopathy
- Can vitamin D be an adjuvant therapy for juvenile rheumatic diseases?
- Classical Dermatomyositis: A Case Report
- Correlation analysis of quantitative MRI measurements of thigh muscles with histopathology in patients with idiopathic inflammatory myopathy
- COVID-19 severity and vaccine breakthrough infections in idiopathic inflammatory myopathies, other systemic autoimmune and inflammatory diseases, and healthy controls: a multicenter cross-sectional study from the COVID-19 Vaccination in Autoimmune Disease
- Dermatomyositis
- Dermatomyositis post vaccine against SARS-COV2
- Displaced Myonuclei in Cancer Cachexia Suggest Altered Innervation
- Effectiveness and safety of mycophenolate mofetil and rituximab combination therapy for immune idiopathic myopathies
- First study demonstrating speckle tracking echocardiography has prognostic value in patients with idiopathic inflammatory myopathies
- High-Dimensional Cytometry Dissects Immunological Fingerprints of Idiopathic Inflammatory Myopathies
- IFN-γ: An overlooked cytokine in dermatomyositis with anti-MDA5 antibodies
- Immunoglobulins in systemic sclerosis management. A large multicenter experience
- Impact of SARS-CoV-2 on the clinical presentation of juvenile idiopathic inflammatory myopathies
- Increased serum levels of sCD40L were associated with rapidly progressive interstitial lung disease in idiopathic inflammatory myopathies
- Interstitial lung disease with and without progressive fibrosing phenotype in patients with idiopathic inflammatory myopathies: data from a large multicentric cohort
- Leveraging Genomic and Bioinformatic Analysis to Enhance Drug Repositioning for Dermatomyositis
- Lung involvement in juvenile idiopathic inflammatory myopathy: A systematic review
- MicroRNAs in idiopathic inflammatory myopathies: state-of-the-art and future perspectives
- Myopathy in a 61-year-old Hispanic man
- Patient-Reported Health-Related Quality of Life, Anxiety and Depression in Patients with Inclusion Body Myositis: A Register-Based Cross-Sectional Study in Germany
- Plasma pentraxin 3 in idiopathic inflammatory myopathies: a possible new biomarker of disease activity
- Polymyositis following varicella and mumps infection in adults: report of two cases
- Pyomyositis Secondary to Localized Cellulitis in a Dermatomyositis Patient: A Case Report and Review of Infectious Complications in Dermatomyositis
- Retinal microvascular abnormalities, cotton wool-like lesions, and macular edema following COVID-19 in a patient previously vaccinated with AstraZeneca and idiopathic myopathy
- Severe onset of inflammatory myositis in a child: think to paraneoplastic myositis
- Spontaneous Development of Immune-Mediated Necrotizing Myopathy (IMNM) After Chronic Use of Statins: A Case Report
- Sporadic Inclusion Body Myositis: MRI Findings and Correlation With Clinical and Functional Parameters
- The Impact of Dysphagia in Myositis: A Systematic Review and Meta-Analysis
- The pattern of MHC class I expression in muscle biopsies from patients with myositis and other neuromuscular disorders
- The role and mechanism of myeloperoxidase in dermatomyositis
- Using peripheral blood immune signatures to stratify patients with adult and juvenile inflammatory myopathies
- Value of the HFA-PEFF diagnostic algorithms for heart failure with preserved ejection fraction to the inflammatory myopathy population