Results 11 to 20 of about 18,649 (278)

Current essentials in inflammatory myopathies [PDF]

open access: yesEuropean Medical Journal Neurology, 2013
Inflammatory myopathies are a heterogeneous group of acquired systemic diseases, which include dermatomyositis (DM), polymyositis (PM), necrotising myopathy (NM) and inclusion body myositis (IBM).
Maren Breithaupt, Jens Schmidt
doaj   +6 more sources

Idiopathic Inflammatory Myopathies [PDF]

open access: yesNeurologic Clinics, 2014
The idiopathic inflammatory myopathies (IIM) consist of rare heterogeneous autoimmune disorders that present with marked proximal and symmetric muscle weakness, except for distal and asymmetric weakness in inclusion body myositis. Despite many similarities, the IIM are fairly heterogeneous from the histopathologic and pathogenetic standpoints, and also
Mazen M, Dimachkie   +2 more
core   +7 more sources

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   +3 more sources

Gene Expression Profiles of Inflammatory Myopathies [PDF]

open access: yesPediatric Neurology Briefs, 2002
The simultaneous expression of 10,000 genes was measured, using Affymetrix GeneChip microarrays, in muscle specimens from 45 patients with various myopathies (dystrophy, congenital myopathy, and inflammatory myopathy) examined at Brigham and Women’s ...
J Gordon Millichap
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

Inflammatory myopathies in the elderly [PDF]

open access: yesEinstein (São Paulo), 2008
Infl ammatory myopathies were analysed according to its differentpresentations, which include dermatomyositis, polymyositis andinclusion body myopathies, especially related to old age.
Edgard Torres dos Reis Neto   +1 more
doaj   +2 more sources

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

Serum levels of matrix metalloproteinases-2 and-9 and their tissue inhibitors in inflammatory neuromuscular disorders [PDF]

open access: yes, 2006
We monitored serum levels of matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) before and during intravenously applied immunoglobulin (IVIG) therapy in 33 patients with chronic immune-mediated neuropathies and myopathies and 15 ...
Mueller-Felber, W.   +3 more
core   +1 more source

The Role of Muscle Biopsy in the Diagnosis of Inflammatory Myopathy [PDF]

open access: yes, 2009
Muscle biopsies of patients with immune-mediated inflammatory myopathies are characterized by a combination of chronic inflammatory infiltrates and muscle fiber necrosis.
Gultekin, Sakir Humayun   +1 more
core   +1 more source

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