Results 21 to 30 of about 45,547 (280)
Pediatric Rheumatology Online Journal, 2017 Objective A pilot study to determine endothelial progenitor cells (EPC) number in children with Juvenile Dermatomyositis (JDM). Methods After obtaining informed consent, the EPC number from 34 fasting children with definite/probable JDM at various stages
Dong Xu +4 more
doaj +1 more source
Pediatric myositis ossificans circumscripta following traumatic hip dislocation: A case report
Radiology Case Reports, 2023 Myositis ossificans is non-neoplastic heterotopic bone forms in skeletal muscle. We recognize 3 subtypes: fibrodysplasia ossificans progressiva, myositis ossificans with no history of trauma (nontraumatic or pseudomalignant), and circumscribed or ...
Khadija Laasri, MD +5 more
doaj +1 more source
Indian Journal of Rheumatology, 2021 Proximal muscle weakness in children, as well as adults, can be the presenting feature of a wide range of diseases including but not limited to the idiopathic inflammatory myopathies, muscle dystrophies, metabolic, endocrine, and drug-induced myopathies. Certain diagnostic clues such as selective muscle involvement in inherited dystrophies, cramping on
Ganguly, Sujata +3 more
openaire +3 more sources
Current Treatment Options in Rheumatology, 2018 A growing body of evidence supports exercise as a very important part of the treatment for adult patients with idiopathic inflammatory myopathies (IIM). This review mainly focuses on exercise studies published during the last 2 years in adult myositis.During the last couple of years, new publications present further evidence for intensive endurance ...
openaire +2 more sources
eJournal of Oral Maxillofacial Research, 2019 Objectives: Heterotopic bone formation within a muscle is designated as ‘myositis ossificans’, and it is associated with multiple aetiologies, such as trauma, genetic predisposition, post-infection, or undetermined causes.
Erika Antonia dos Anjos Ramos +4 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 +2 more
doaj +1 more source
Arthritis & Rheumatism, 2006 AbstractMyositis has been reported as a rare manifestation of Lyme disease, and Lyme myositis can be an important consideration in the differential diagnosis of unusual cases, especially in patients who live in or travel to endemic areas. We report the case of a 43‐year‐old man who presented with focal myositis of the proximal lower extremity and was ...
Aaron R, Holmgren, Eric L, Matteson
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Idiopathic Orbital Myositis in a Child
, 2013 Idiopathic orbital myositis is seen very rare in children. In this article, the diagnose criteria of a pediatric case with idiopathic orbital myositis and oral non-steroid anti-inflammatory treatment’s response have been evaluated.
Burak Ulaş, Özlem Alkan, Aysel Pelit
core +1 more source
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