Results 21 to 30 of about 18,649 (278)

Paraneoplastic Necrotizing Myopathy with a Mild Inflammatory Component: A Case Report and Review of the Literature

Case Reports in Oncology, 2010
Inflammatory myopathies such as dermatomyositis and polymyositis are well-recognized paraneoplastic syndromes. Little is known, however, about necrotizing myopathies in association with cancer.
Susanne Wegener, Juliane Bremer, Paul Komminoth, Hans H. Jung, Michael Weller   +4 more
doaj   +1 more source

Delayed skeletal muscle repair following inflammatory damage in simulated agent-based models of muscle regeneration.

PLoS Computational Biology, 2023
Healthy skeletal muscle undergoes repair in response to mechanically localised strains during activities such as exercise. The ability of cells to transduce the external stimuli into a cascade of cell signalling responses is important to the process of ...
Stephanie Khuu, Justin W Fernandez, Geoffrey G Handsfield   +2 more
doaj   +1 more source

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, Tatiana Cobo-Ibáñez, Iolanda Prats Caelles   +2 more
doaj   +1 more source

Polymyositis and dermatomyositis: Disease spectrum and classification

Indian Journal of Dermatology, 2012
Muscle inflammation and weakness are the key features of idiopathic inflammatory myopathies (IIMs). In addition IIMs are frequently associated with cutaneous and pulmonary involvement. In clinical practice the three common inflammatory myopathies we come
Siba P Raychaudhuri, Anupam Mitra
doaj   +1 more source

Current pharmacological treatment of idiopathic inflammatory myopathies [PDF]

, 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   +3 more sources

Nonimmune mechanisms in idiopathic inflammatory myopathies [PDF]

, 2020
This review encompasses the main novelties regarding nonimmune mechanisms implicated in the pathogenesis of idiopathic inflammatory myopathies (IIM)
Sandra Zampieri, Zampieri, Sandra, Doria, Andrea, Chiara Franco, Marta Loredo Martinez, Loredo Martinez, Marta, Franco, Chiara, Anna Ghirardello, Gatto, Mariele, Andrea Doria, Ghirardello, Anna, Mariele Gatto   +11 more
core   +1 more source

Resistin in idiopathic inflammatory myopathies [PDF]

, 2012
: INTRODUCTION: To evaluate and compare the serum levels and local expression of resistin in patients with idiopathic inflammatory myopathies to controls, and to determine the relationship between resistin levels, inflammation and disease activity ...
Filkova, Maria, Andrés Cerezo, Lucie, Vencovsky, Jiri, Hulejova, Hana, Plestilova, Lenka, Mann, Herman, Senolt, Ladislav, Kuncova, Klara, Gay, Steffen, Klein, Martin, Zamecnik, Josef   +10 more
core   +1 more source

Demographic characteristics of 103 patients with inflammatory myopathies. [PDF]

, 2023
Demographic characteristics of 103 patients with inflammatory myopathies.
Seung-Ah Lee (11177545), Byeol-A Yoon (8537949), Hyun Joon Lee (15295250), Seung Woo Kim (8671644), Bum Chun Suh (15295253), Hyung Jun Park (4922989), Ha Young Shin (8671647), Young-Chul Choi (3331461)   +7 more
core   +1 more source

Inflammatory myopathies: an update for neurologists

Arquivos de Neuro-Psiquiatria, 2022
Idiopathic inflammatory myopathies (IIM) are a heterogenous group of treatable myopathies. Patients present mainly to the rheumatologist and neurologists, complaining of acute or subacute onset of proximal weakness. Extramuscular manifestations may occur,
André Macedo Serafim Silva, Eliene Dutra Campos, Edmar Zanoteli   +2 more
doaj   +1 more source

Autoantibody testing in idiopathic inflammatory myopathies [PDF]

, 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., Engelen, B.G.M. van, Lim, J., Kooi, A. van der, Visser, M de, Benveniste, O., Pruijn, G., Rietveld, A.   +7 more
core   +1 more source