Spatial transcriptomics reveals mechanism of autoimmunity driven by internalized autoantibodies

Phosphodiesterase 4 (PDE 4) Inhibition Reduces Ischemia-Reperfusion-Induced Leucocyte Infiltration, Apoptosis and Mitochondrial Fission Markers in Mice Skeletal Muscles Four Hours After Ischemia Onset

Acute Severe Hypoxia Decreases Mitochondrial Chain Complex II Respiration in Human Peripheral Blood Mononuclear Cells

Early anticoagulant resumption after atypical intracerebral hemorrhage: beyond atrial fibrillation analysis of two clinical cases admitted to the University Hospital of Pisa

Impaired Peripheral Blood Mononuclear Cell (PBMC) Mitochondrial Respiration Is Associated with Mortality and Long COVID Syndrome Severity in COVID-19 Patients

The role of multicriteria decision analysis in the development of candidate classification criteria for antisynthetase syndrome: analysis from the CLASS project

Enhanced proteasome activity in perifascicular myofibres is a hallmark of dermatomyositis and its inhibition is efficient in preclinical models

Aquaporin-4 downregulation in dysphagic patients with idiopathic inflammatory myopathies: myofiber vulnerability and inflammation drivers

Revisiting the link between oropharyngeal dysphagia and cancer in autoimmune myositis: a descriptive study

Response to: 'Lipid droplets at center stage in IMNM? - An ultrastructural 2D large scale quantification' by Focks et al. New insights into pathology, serology, and pathophysiology highlight IMNM as a heterogeneous group of inflammatory myopathies

Appendicular Lean Mass Index Using Dual-Energy X-Ray Absorptiometry (DEXA) in Professional Football: A Pilot Study of a New Method for Improved Inter-Operator Reproducibility and Analysis of Pelvi-Trochanteric Muscles

In immune-mediated necrotising myopathy, anti-HMGCR antibodies inhibit HMGCR activity, leading to the sarcoplasmic accumulation of lipid droplets and myofibres necrosis

Experimental myositis: an optimised version of C-protein-induced myositis

The classification of myositis: setting the stage for a universal terminology

Anti-SAE dermatomyositis: clinical and histologic characteristics from a monocentric Italian cohort

Clinical, histologic and prognostic features of clinically amyopathic dermatomyositis

Comment on: Inaugural dropped head syndrome and camptocormia in inflammatory myopathies: a retrospective study

Cannabis (THC) Aggravates the Deleterious Effects of Alcohol (EtOH) on Skeletal Muscles' Mitochondrial Respiration: Modulation by Age and Metabolic Phenotypes

Sarcopenia assessed by DXA and hand-grip dynamometer: a potential marker of damage, disability and myokines imbalance in inflammatory myopathies

IFNγ causes mitochondrial dysfunction and oxidative stress in myositis

Targeting Mitochondrial Dynamics during Lower-Limb Ischemia Reperfusion in Young and Old Mice: Effect of Mitochondrial Fission Inhibitor-1 (mDivi-1)

Agreement between local and central anti-synthetase antibodies detection: results from the Classification Criteria of Anti-Synthetase Syndrome project biobank

In inflammatory myopathies, dropped head/bent spine syndrome is associated with scleromyositis: an international case-control study

Perivascular and endomysial macrophages expressing VEGF and CXCL12 promote angiogenesis in anti-HMGCR immune-mediated necrotizing myopathy

Long Term Follow-Up of Sarcopenia and Malnutrition after Hospitalization for COVID-19 in Conventional or Intensive Care Units

Clinical spectrum time course in non-Asian patients positive for anti-MDA5 antibodies

Capillary pathology with prominent basement membrane reduplication is the hallmark histopathological feature of scleromyositis

Scleromyositis: A distinct novel entity within the systemic sclerosis and autoimmune myositis spectrum. Implications for care and pathogenesis

Resolution of Inflammation after Skeletal Muscle Ischemia-Reperfusion Injury: A Focus on the Lipid Mediators Lipoxins, Resolvins, Protectins and Maresins

Long-term efficacy of adding intravenous immunoglobulins as treatment of refractory dysphagia related to myositis: a retrospective analysis

Severe muscle damage with myofiber necrosis and macrophage infiltrates characterize anti-Mi2 positive dermatomyositis

Similarities between COVID-19 and anti-MDA5 syndrome: what can we learn for better care?

Influence of Antisynthetase Antibodies Specificities on Antisynthetase Syndrome Clinical Spectrum Time Course

Nailfold Capillaroscopy Characteristics of Antisynthetase Syndrome and Possible Clinical Associations: Results of a Multicenter International Study

Autophagy markers LC3 and p62 accumulate in immune-mediated necrotizing myopathy

Timing of onset affects arthritis presentation pattern in antisyntethase syndrome

Clinical follow-up predictors of disease pattern change in anti-Jo1 positive anti-synthetase syndrome: Results from a multicenter, international and retrospective study

A New Immunodot Assay for Multiplex Detection of Autoantibodies in a Cohort of Italian Patients With Idiopathic Inflammatory Myopathies

Prevalence and Clinical Correlates of Sarcopenia and Malnutrition in Lung Transplant Recipients Using EWGSOP2 and GLIM Criteria

Current classification criteria underestimate the incidence of idiopathic inflammatory myopathies by ignoring subgroups

Refining Incidence and Characteristics of Inflammatory Myopathies: A Quadruple-Source Capture-Recapture Survey Using the 2017 European League Against Rheumatism/American College of Rheumatology Classification Criteria

Incidence and predictors of COVID-19 and flares in patients with rare autoimmune diseases: a systematic survey and serological study at a national reference center in France

Inclusion body myositis and Sjögren's syndrome: the association works both ways

Significance of Sjögren's syndrome and anti-cN1A antibody in myositis patients

Comment on: Refining myositis associated with primary Sjögren's syndrome: data from the prospective cohort ASSESS: Reply

Refining myositis associated with primary Sjögren's syndrome: data from the prospective cohort ASSESS

Histopathological features of systemic sclerosis-associated myopathy: A scoping review

Sarcopenia and peripheral arterial disease: a systematic review

Serum Jo-1 Autoantibody and Isolated Arthritis in the Antisynthetase Syndrome: Review of the Literature and Report of the Experience of AENEAS Collaborative Group

[Increased circulating level of fatty acid-binding protein 3 (FABP3): a potential biomarker of muscle damage in inflammatory myopathies patients]

Thrombocytopenia in idiopathic inflammatory myopathies: a case series analysis

Sarcopenia and peripheral arterial disease: a systematic review