Results 51 to 60 of about 45,547 (280)

Immune-Mediated Necrotizing Myopathy Associated With Myelodysplastic Syndrome

open access: yesAnnals of Internal Medicine: Clinical Cases, 2023
Autoimmune diseases can often be diagnosed in patients with myelodysplastic syndrome (MDS). Here, we review the emerging literature linking MDS and rare presentations of autoimmunity, including myositis.
Katherine M. Sheu   +3 more
doaj   +1 more source

The diagnostic utility of myositis autoantibody testing for predicting the risk of cancer-associated myositis [PDF]

open access: yes, 2007
Objectives: There is a known association between myositis and cancer. The risk is greater in dermatomyositis (DM) than polymyositis (PM), although reliable methods to predict cancer risk in specific patients with myositis are not presently available ...
Fertig, Noreen   +4 more
core   +1 more source

Discordance Between Patient and Physician Global Assessments in Early Systemic Sclerosis

open access: yesArthritis Care &Research, EarlyView.
Objective This study aims to identify factors associated with patient global assessment (PtGA) and physician global assessment (PhGA) and discordance between them in systemic sclerosis (SSc). Methods Data from adults with early SSc (<5 years) from the Collaborative National Quality and Efficacy Registry were included.
Ellen Romich   +35 more
wiley   +1 more source

Baricitinib could improve the prognosis of anti-MDA5 antibody positive dermatomyositis associated interstitial lung disease

open access: yesArthritis Research & Therapy
Background and objective Currently, there are only a few effective treatments for anti-melanoma differentiation-associated gene 5 antibody (anti-MDA5) positive dermatomyositis (DM)-associated interstitial lung disease (ILD).
Shuai Zhu   +7 more
doaj   +1 more source

Idiopathic inflammatory myopathy: From muscle biopsy to serology

open access: yesIndian Journal of Rheumatology, 2020
Idiopathic inflammatory myopathies (IIMs) are heterogeneous group of muscle disorders characterized by variable degree of muscle weakness and muscle inflammation. Various classification systems have been proposed for myositis.
Ritu Verma, Vimal Kumar Paliwal
doaj   +1 more source

Discordance Between Systemic Lupus Erythematosus Disease Activity Index Domain Weights and Their Association With Organ Damage Accrual

open access: yesArthritis Care &Research, EarlyView.
Objective Studies of damage accrual in patients with systemic lupus erythematosus (SLE) show associations with disease activity measured by the SLE Disease Activity Index 2000 (SLEDAI‐2K), but these associations are imperfect. SLEDAI scores are powerfully influenced by weightings (1–8) assigned to each domain.
Kevin Zhang   +8 more
wiley   +1 more source

Tongue myositis in dermatomyositis with anti-PM-Scl 75 antibody: two case reports

open access: yesBMC Musculoskeletal Disorders
Background Dermatomyositis (DM) is a heterogeneous disease characterized by skin rash and muscle weakness. Although tongue disorders have been documented in idiopathic inflammatory myopathies (IIM), biopsy-confirmed tongue myositis remains exceedingly ...
Chao Sun   +4 more
doaj   +1 more source

Predictive value of myositis antibodies: role of semiquantitative classification and positivity for more than one autoantibody

open access: yesRMD Open
Objectives We assessed the positive predictive value (PPV) of 17 myositis antibodies for having a diagnosis of myositis and other myositis-spectrum conditions (interstitial lung disease (ILD), connective tissue diseases (CTD), malignancy) and evaluated ...
Anne M Kerola   +4 more
doaj   +1 more source

Clinical types of lung disease in polymyositis and dermatomyositis

open access: yesКлинический разбор в общей медицине, 2021
The idiopathic inflammatory myopathies are a group of rare, heterogeneous connective tissue disorders characterized by skeletal muscle inflammation. The four main forms of idiopathic inflammatory myopathies are dermatomyositis, polymyositis, inclusion ...
Inna B. Bondarenko   +2 more
doaj   +1 more source

Myositis in the course of the systemic form juvenile idiopathic arthritis

open access: yes, 2014
The systemic juvenile idiopathic arthritis (SJIA) represents approximately 10% of all cases of JIA, there is no difference in onset rate between boys and girls.
Barbara Lisowska   +2 more
core   +1 more source

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