Cardiovascular manifestations in idiopathic inflammatory myopathies [PDF]
, 2023 Cardiovascular involvement in idiopathic inflammatory myopathies (IIM) is an understudied area which is gaining increasing recognition in recent times.
Shah, Meera +7 more
core +1 more source
High-Dimensional Cytometry Dissects Immunological Fingerprints of Idiopathic Inflammatory Myopathies
Cells, 2022 Chronic inflammation of skeletal muscle is the common feature of idiopathic inflammatory myopathies (IIM). Given the rarity of the disease and potential difficulty of routinely obtaining target tissue, i.e., standardized skeletal muscle, our ...
Christopher Nelke +14 more
doaj +1 more source
Top ten discoveries of the year: Neuromuscular disease
Free Neuropathology, 2020 This review highlights ten important advances in the neuromuscular disease field that either were first reported in 2019, or have reached a broad consensus during that year.
Marta Margeta
doaj +1 more source
Long term functional outcome of idiopathic inflammatory myopathies
Reumatismo, 2001 The idiopathic inflammatory myopathies (IIM) comprise a group of diseases characterized by chronic inflammation of the skeletal muscles. The definition of the long-term outcome of IIM, has been limited by the difficulty in objectively evaluating the rate
R. Neri +5 more
doaj +1 more source
Survival and cancer risk in an unselected and complete Norwegian idiopathic inflammatory myopathy cohort [PDF]
, 2015 Objective To utilise an exposed/unexposed cohort strategy for mortality and cancer analyses across unselected and complete cohorts of patients with idiopathic inflammatory myopathy (IIM) resident in south-east Norway (denominator population 2.6 million),
Gran, Jan Tore +4 more
core +1 more source
Respiratory disorders in patients with polymyositis/dermatomyositis
Современная ревматология, 2014 Idiopathic inflammatory myopathies (IIM) are rare disorders characterized by inflammatory lesions in skeletal muscles. These diseases include polymyositis (PM), dermatomyositis (DM), and inclusion body myositis, which exhibit clinicoimmunological ...
Olga Alekseyevna Antelava +3 more
doaj +1 more source
Patient global assessment and inflammatory markers in patients with idiopathic inflammatory myopathies – A longitudinal study [PDF]
Aim: To explore if patient global assessment (PGA) is associated with inflammation over time and if associations are explained by other measures of disease activity and function in patients with idiopathic inflammatory myopathies (IIM).Methods: PGA and ...
Mercado m．, Vazquez-Del +39 more
core +1 more source
Muscle biopsy features of idiopathic inflammatory myopathies and differential diagnosis [PDF]
, 2014 The gold standard to characterize idiopathic inflammatory myopathies is the morphological, immunohistochemical and immunopathological analysis of muscle biopsy.
VATTEMI, Gaetano Nicola +6 more
core +1 more source
Necrotizing Autoimmune Myopathy: A Rare Variant of Idiopathic Inflammatory Myopathies [PDF]
, 2017 Idiopathic inflammatory myopathies are an unusual group of myopathies with annual incidence of 1 in 100 000 people in the United States. Necrotizing autoimmune myopathy comprises only 16% of this group.
Samer Makhoul MD +4 more
core +3 more sources
A rare case of juvenile dermatomyositis and review of literature
Indian Journal of Paediatric Dermatology, 2017 Idiopathic inflammatory myopathies are rare group of systemic connective tissue diseases. The hallmark of these disorders is symmetrical chronic inflammation and weakness of proximal muscles. Juvenile dermatomyositis (JDM) is the most common inflammatory
Anjali T Bharani +3 more
doaj +1 more source