Results 211 to 220 of about 20,247 (257)

Disease activity in patients with idiopathic inflammatory myopathy according to time since diagnosis and positivity to antisynthetase autoantibodies: data from the Myo-Spain registry. [PDF]

open access: yesArthritis Res Ther
Cobo-Ibáñez T   +51 more
europepmc   +1 more source

Environmental triggers for idiopathic inflammatory myopathies: unravelling the known and unknown

open access: bronze
Chiara Cardelli   +7 more
openalex   +2 more sources

[Autoantibody diagnostics in idiopathic inflammatory myopathy]. [PDF]

open access: yesZ Rheumatol
Biesen R   +3 more
europepmc   +1 more source

Muscle Tissue Transcriptome of Idiopathic Inflammatory Myopathy Reflects the Muscle Damage Process by Monocytes and Presence of Skin Lesions. [PDF]

open access: yesArthritis Rheumatol
Izuka S   +21 more
europepmc   +1 more source

The Prospective Registry Of MyositIS (PROMIS): II. Temporal shifts in causes of death among patients with idiopathic inflammatory myopathies

open access: hybrid
Yu Chen   +22 more
openalex   +1 more source

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

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