Results 231 to 240 of about 66,787 (287)

Long-Term Dysphagia Severity in Patients With Idiopathic Inflammatory Myopathy: A Single-Center Retrospective Study. [PDF]

Cureus
Ohmura SI, Sato K, Nishimura R, Miyamoto T.   +3 more
europepmc   +1 more source

Efficacy and Safety of Subcutaneous Abatacept Plus Standard Treatment for Active Idiopathic Inflammatory Myopathy: Phase 3 Randomized Controlled Trial. [PDF]

Arthritis Rheumatol
Aggarwal R, Lundberg IE, Song YW, Shaibani A, Werth VP, Maldonado MA.   +5 more
europepmc   +1 more source

Belimumab treatment of adult idiopathic inflammatory myopathy. [PDF]

Rheumatology (Oxford)
Marder G, Quach T, Chadha P, Nandkumar P, Tsang J, Levine T, Schiopu E, Furie R, Davidson A, Narain S.   +9 more
europepmc   +1 more source

Disease characteristics and medications use in idiopathic inflammatory myopathy: a multi-centre prospective observational study of decentralized remote vs. traditional clinic enrolment. [PDF]

Rheumatology (Oxford)
Keret S, Silva RL, Chandra T, Gkiaouraki E, Pongtarakulpanit N, Sriram S, Moghadam-Kia S, Oddis CV, Aggarwal R.   +8 more
europepmc   +1 more source

Contribution of major histocompatibility complex class II immunostaining in distinguishing idiopathic inflammatory myopathy subgroups: A histopathological cohort study. [PDF]

J Neuropathol Exp Neurol
Lessard LER, Robert M, Fenouil T, Mounier R, Landel V, Carlesimo M, Hot A, Chazaud B, Laumonier T, Streichenberger N, Gallay L.   +10 more
europepmc   +1 more source

Development of a machine learning model in prediction of the rapid progression of interstitial lung disease in patients with idiopathic inflammatory myopathy. [PDF]

Quant Imaging Med Surg
Qiang Y, Wang H, Ni Y, Wang J, Liu A, Yang H, Xi L, Ren Y, Xie B, Wang S, Liu M, Wang C, Dai H.   +12 more
europepmc   +1 more source

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Inflammatory Myopathies

Continuum, 2006
To discuss the clinical, laboratory, and histopathologic features and presumed pathogenic mechanisms of the four major categories of idiopathic inflammatory myopathy, namely dermatomyositis, polymyositis, immune-mediated necrotizing myopathy, and inclusion body myositis.Dermatomyositis, polymyositis, necrotizing myopathy, and inclusion body myositis ...
Anthony A, Amato, Steven A, Greenberg
openaire   +4 more sources

INFLAMMATORY MYOPATHIES

Acta Clinica Belgica, 2004
Primary myositis (or inflammatory myopathies) comprises three main groups of diseases, based on clinical and immunohistochemical characteristics: polymyositis (PM), dermatomyositis (DM) and inclusion body myositis. Their clinical presentation and course are disparate, but a common characteristic is immune dysfunction-related inflammation of the ...
Patrick M., Grogan, Jonathan S., Katz
openaire   +5 more sources