Results 11 to 20 of about 1,119,241 (175)

Disease Specific Autoantibodies in Idiopathic Inflammatory Myopathies [PDF]

open access: yesFrontiers in Neurology, 2019
Idiopathic inflammatory myopathies represent still a diagnostic and therapeutic challenge in different disciplines including neurology, rheumatology, and dermatology.
Bruno Stuhlmüller   +4 more
doaj   +2 more sources

DISABILITY IN PATIENTS WITH IDIOPATHIC INFLAMMATORY MYOPATHIES [PDF]

open access: yesArchives of the Balkan Medical Union, 2019
Introduction. Idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of disorders, characterized by chronic muscle weakness, low muscle endurance and by the presence of inflammatory cell infiltrates in muscle tissue, with organ damage and ...
Natalia LOGHIN-OPREA   +5 more
doaj   +3 more sources

Immunosuppressive and immunomodulatory therapies for idiopathic inflammatory myopathies [PDF]

open access: yes, 2023
Objectives: This is a protocol for a Cochrane Review (intervention). The objectives are as follows:. This protocol is for two separate reviews to assess the effects (benefits and harms) of immunosuppressant and immunomodulatory treatments for the ...
Gullick, Nj   +12 more
core   +1 more source

Adult idiopathic inflammatory myopathies [PDF]

open access: yes, 2022
The idiopathic inflammatory myopathies represent a rare group of diseases characterized by autoimmune inflammation of skeletal muscle and other organs. There has been significant recent progress in understanding pathogenesis, phenotyping disease subtypes
Chinoy, Hector; id_orcid   +2 more
core   +1 more source

A national registry for juvenile dermatomyositis and other paediatric idiopathic inflammatory myopathies: 10 years' experience; the Juvenile Dermatomyositis National (UK and Ireland) Cohort Biomarker Study and Repository for Idiopathic Inflammatory Myopathies [PDF]

open access: yes, 2010
Objectives: The paediatric idiopathic inflammatory myopathies (IIMs) are a group of rare chronic inflammatory disorders of childhood, affecting muscle, skin and other organs.
Juvenile Dermatomyositis Research Group   +15 more
core   +1 more source

Arthrogenic Alphaviruses and Inflammatory Myopathies [PDF]

open access: yes, 2011
There is increasing evidence to suggest that viruses have aetiological roles in the idiopathic inflammatory myopathies. Arthrogenic alphaviruses (such as chikungunya virus, Ross River virus and sindbis virus) are known to cause outbreaks of polyarthritis
Suresh Mahalingam   +3 more
core   +1 more source

Current pharmacological treatment of idiopathic inflammatory myopathies [PDF]

open access: yes, 2016
The idiopathic inflammatory myopathies are uncommon and heterogeneous disorders. Their classification is based on distinct clinicopathologic features.
Fasano, S, Isenberg, DA, Alves, SC
core   +2 more sources

AASLD practice guidance on drug, herbal, and dietary supplement–induced liver injury

open access: yes, 2022
Hepatology, EarlyView.
Robert J. Fontana   +6 more
wiley   +1 more source

Autoantibody testing in idiopathic inflammatory myopathies [PDF]

open access: yes, 2019
Contains fulltext : 207009.pdf (Publisher’s version ) (Open Access)The diagnosis and classification of idiopathic inflammatory myopathies are based mainly on clinical and histological features.
Saris, C.G.J.   +7 more
core   +1 more source

Case of Polymyositis Associated with Celiac Disease: A Case Report

open access: yesPakistan Armed Forces Medical Journal, 2023
Polymyositis is an important subtype of idiopathic inflammatory myopathies characterized by muscle inflammation andweakness, often associated with other systemic diseases and malignancies.
Abdul Rehman Azeem   +4 more
doaj   +1 more source

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