Results 31 to 40 of about 62,398 (280)
Cutaneous manifestations in idiopathic inflammatory myopathies
Journal of IMIDs, 2022 Idiopathic inflammatory myopathies (IIMs), also known as autoimmune myositis, are a rare group of autoimmune disorders with a heterogenoeous spectrum of muscular and extramuscular involvement. IIM can be classified into several subgroups: dermatomyositis
Juan Sanz-Correa +2 more
doaj +1 more source
Nuclear matrix protein 2 antibody-positive adult dermatomyositis: a case report and review of the literature [PDF]
, 2020 Dermatomyositis is a clinically heterogenous inflammatory myopathy with unique cutaneous features. Myositis-specific antibodies can aid in diagnosis and anticipation of patient prognosis.
Cartron, Alexander M +3 more
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Inclusion body myositis: therapeutic approaches. [PDF]
, 2012 The idiopathic inflammatory myopathies are a heterogeneous group of diseases that include dermatomyositis (DM), polymyositis (PM), inclusion body myositis (IBM) and other less common myopathies.
Aggarwal, Rohit, Oddis, Chester V
core +1 more source
Focal Myositis in paediatric age. [PDF]
, 2015 BACKGROUND: Focal Myositis is a rare pseudotumor of unknown aetiology that is often difficult to diagnose and treat. Typically afflicting people in adulthood, it has occasionally been reported also among children.
Alaggio, Rita, Corradin, M, Gigante, C
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Review of presentations at the 6th European Lupus Meeting 3-5 March 2005. [PDF]
, 2005 The 6th European Lupus Meeting was held at the Royal College of Physicians of London and was attended by 450 delegates. The conference brought together leading speakers from Europe and North America who reviewed current knowledge and exciting new ...
Bowman, SJ +3 more
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An Outbreak of Acute Viral Myositis with Different Outcomes: A Case Series
Journal of Integrated Health Sciences, 2019 Viral myositis is induced by direct muscle invasion, molecular mimicry, production of immune complexes, immune dysregulation, and various other mechanisms. The pathogenesis of this entity is still unclear.
Divya Goel, Arvind Vyas, Naveen Seervi
doaj +1 more source
Rhabdomyolysis in an HIV cohort: epidemiology, causes and outcomes. [PDF]
, 2017 BackgroundThe Literature on rhabdomyolysis in the HIV-positive population is sparse and limited. We aimed to explore the incidence, patient characteristics, etiologies and outcomes of rhabdomyolysis in a cohort of HIV-positive patients identified through
Atta, Mohamed G +6 more
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Dermatomyositis and Immune-Mediated Necrotizing Myopathies: A Window on Autoimmunity and Cancer
Frontiers in Immunology, 2017 Autoimmune myopathies (myositides) are strongly associated with malignancy. The link between myositis and cancer, originally noticed by Bohan and Peter in their classification in 1975 (1), has been evidenced by large population-based cohort studies and a
Audrey Aussy +3 more
doaj +1 more source
Cancer Treatment and Research Communications, 2020 Background: Lung cancer is the second most common cancer in both men and women and the leading cause of cancer death worldwide. The development of novel tyrosine kinase inhibitors (TKIs) represented a paradigm shift in the management of lung cancer and ...
Pawel Parafianowicz +4 more
doaj +1 more source
Concomitant occurrence of FXTAS and clinically defined sporadic inclusion body myositis: report of two cases. [PDF]
, 2017 This report describes unique presentations of inclusion body myositis (IBM) in two unrelated patients, one male and one female, with genetically and histologically confirmed fragile X-associated tremor/ataxia syndrome (FXTAS).
Bolitho, Samuel J +11 more
core +2 more sources