Results 171 to 180 of about 18,065 (215)

Contribution of major histocompatibility complex class II immunostaining in distinguishing idiopathic inflammatory myopathy subgroups: A histopathological cohort study. [PDF]

J Neuropathol Exp Neurol
Lessard LER, Robert M, Fenouil T, Mounier R, Landel V, Carlesimo M, Hot A, Chazaud B, Laumonier T, Streichenberger N, Gallay L.   +10 more
europepmc   +1 more source

Disease characteristics and medications use in idiopathic inflammatory myopathy: a multi-centre prospective observational study of decentralized remote vs. traditional clinic enrolment. [PDF]

Rheumatology (Oxford)
Keret S, Silva RL, Chandra T, Gkiaouraki E, Pongtarakulpanit N, Sriram S, Moghadam-Kia S, Oddis CV, Aggarwal R.   +8 more
europepmc   +1 more source

Atherosclerotic cardiovascular disease following a diagnosis of idiopathic inflammatory myopathy: analysis from a retrospective cohort in the TriNetX registry. [PDF]

Clin Rheumatol
Allenzara A, Jicha K, Álvarez C, Nelson A, Foulke G.   +4 more
europepmc   +1 more source

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Idiopathic inflammatory myopathies

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,
Ingrid E. Lundberg, Manabu Fujimoto, Jiri Vencovsky, Rohit Aggarwal, Marie Holmqvist, Lisa Christopher-Stine, Andrew L. Mammen, Frederick W. Miller   +7 more
exaly   +9 more sources

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
  +5 more sources

IDIOPATHIC INFLAMMATORY MYOPATHIES

Neurologic Clinics, 1997
Dermatomyositis, polymyositis, and inclusion body myositis are the major categories of idiopathic inflammatory myopathy. These inflammatory myopathies are distinct clinically, histologically, and pathogenically. Features of dermatomyositis and polymyositis can overlap with those of other autoimmune connective tissue diseases.
A A, Amato, R J, Barohn
openaire   +4 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.
  +5 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

Rheumatic Disease Clinics of North America, 2019
Major advances have been made in the field of idiopathic inflammatory myopathies (IIM), or myositis, that are likely to facilitate development of new therapeutic strategies that have not yet been applied in this group of diseases. These advances include new classification criteria to better identify the patients with IIM, detection of several new ...
Jiří, Vencovský, Helene, Alexanderson, Ingrid E, Lundberg   +2 more
openaire   +2 more sources

Idiopathic Inflammatory Myopathies

2008
Major pathology consists of focal inhomogeneous infl ammation with injury, death, and repair of muscle cells. Each subgroup of myositis has characteristic changes on microscopy and immunochemistry. ■ Etiology is still unclear but selected environmental exposures in genetically predisposed hosts have been found.
Lisa G. Rider, Frederick W. Miller
  +5 more sources