Results 141 to 150 of about 9,523 (188)

Idiopathic inflammatory myopathies lack neutralising autoantibodies to type- I, II and III interferons. [PDF]

RMD Open
Behere A, Mildner H, Peralta Garcia I, Pérez Bucio C, Lundberg I, Horuluoglu B, Landegren N.   +6 more
europepmc   +1 more source

IgG subclass-specific N-glycosylation differentiates HRCT subtypes in idiopathic inflammatory myopathies-associated ILD. [PDF]

Front Immunol
Wu T, Li Y, Ling Y, Luo Y, Wu Y, Zhao J, Cheng L, Tan C, Zhang Y, Liu Y.   +9 more
europepmc   +1 more source

Evaluating the Diagnostic Potential of Myxovirus Resistance Protein 1 (MX1) and Myxovirus Resistance Protein 2 (MX2) As Biomarkers in Idiopathic Inflammatory Myopathies. [PDF]

Cureus
Neupane R, Haider M, Smith P, Kesselman MM.   +3 more
europepmc   +1 more source

Barriers and facilitators to exercise in people with idiopathic inflammatory myopathies: a qualitative study. [PDF]

BMC Rheumatol
Li N, Frade S, Roper L, Parker MJ, Youssef P, Nikpour M.   +5 more
europepmc   +1 more source

Idiopathic inflammatory myopathies [PDF]

Nature Reviews Disease Primers, 2021
Idiopathic inflammatory myopathies (IIM), also known as myositis, are a heterogeneous group of autoimmune disorders with varying clinical manifestations, treatment responses and prognoses. Muscle weakness is usually the classical clinical manifestation but other organs can be affected, including the skin, joints, lungs, heart and gastrointestinal tract,
Íngrid E Lundberg, Manabu Fujimoto, J Vencovsky   +2 more
exaly   +6 more sources

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Idiopathic Inflammatory Myopathies

Indian Journal of Pediatrics, 2023
Idiopathic inflammatory myopathies (IIMs) are a diverse group of diseases characterized by proximal muscle weakness and inflammation in skeletal muscle. Phenotypically, the subtypes include dermatomyositis, polymyositis, inclusion body myositis, and amyopathic dermatomyositis. The most common IIM in children is juvenile dermatomyositis (JDM).
Suma Balan, Sumanth Madan
openaire   +3 more sources

Epidemiology of the idiopathic inflammatory myopathies

Nature Reviews Rheumatology, 2023
The idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of systemic autoimmune diseases that affect the skeletal muscles and can also involve the skin, joints, lungs and heart. The epidemiology of IIM is obscured by changing classification criteria and the inherent shortcomings of case identification using healthcare record diagnostic ...
Thomas Khoo, James B Lilleker, Bernard Yu-Hor Thong   +2 more
exaly   +4 more sources

Idiopathic inflammatory myopathies

Best Practice & Research Clinical Rheumatology, 2012
Inflammatory myopathies are chronic, immune-mediated diseases characterised by progressive proximal muscle weakness. They encompass a variety of syndromes with protean manifestations. The diagnosis is based on Bohan and Peter's classification criteria, which nowadays seem to be obsolete.
Melinda, Vincze, Katalin, Danko
openaire   +2 more sources

Idiopathic Inflammatory Myopathies

Rheumatic Disease Clinics of North America, 1990
The idiopathic inflammatory myopathies are a heterogeneous group of uncommon diseases. The incidence rate of IIM is approximately 5 cases per million population, but there appears to be an increase in the rate over the last two decades, particularly in black females.
M E, Cronin, P H, Plotz
openaire   +2 more sources

Idiopathic Inflammatory Myopathies

DeckerMed Neurology, 2002
The idiopathic inflammatory myopathies (IIMs), also known as myositis syndromes, are a collection of heterogeneous disorders that share the common feature of chronic muscle inflammation of unknown cause. These disorders may occur in adults or children and are sometimes associated with other connective tissue disorders and a variety of cancers.
openaire   +2 more sources