Results 151 to 160 of about 45,547 (280)
, 1999 We report a case of myositis presenting as an apparently unique progressive facial weakness. The only biological abnormality after an 8-year follow-up was an immunocytoma. Molecular analyses excluded facioscapulohumeral muscular dystrophy.
Janzer, R.C. +3 more
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Muscle &Nerve, Volume 74, Issue 1, Page 131-138, July 2026.ABSTRACT Introduction/Aims Inclusion body myositis (IBM) is an inflammatory myopathy with an insidious onset, often making diagnosis challenging. Although neuroimaging has recently been included in diagnostic criteria, the role of muscle ultrasound—despite being a rapid and cost‐effective tool—in IBM has been less extensively characterized.
Giuseppe Di Pietro +11 more
wiley +1 more source
The myositis autoantibody phenotypes of the juvenile idiopathic inflammatory myopathies.
, 2013 The juvenile idiopathic inflammatory myopathies (JIIM) are systemic autoimmune diseases characterized by skeletal muscle weakness, characteristic rashes, and other systemic features.
Rider, Lisa G, LG;Shah, Mona, M;Mamyrova, Gulnara, G;Huber, Adam M, AM;Rice, Madeline Murguia, MM;Targoff, Ira N, IN;Miller, Frederick W, FW;Childhood Myositis Heterogeneity Collaborative Study Group
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Clinical Genetics, Volume 110, Issue 1, Page 15-28, July 2026.Advances in genomic, proteomic, and transcriptomic technologies are transforming the diagnosis of genetic myopathies. When integrated with traditional muscle pathology, multi‐omics approaches improve diagnostic yield, clarify disease mechanisms, and support more precise, mechanism‐based therapeutic strategies for patients with neuromuscular disorders ...
Ludmila Alem +2 more
wiley +1 more source
Immune‐Driven Expression in Inclusion Body Myositis With T‐Cell Large Granular Lymphocytic Leukemia
Annals of Clinical and Translational Neurology, Volume 13, Issue 6, Page 1196-1205, June 2026.ABSTRACT Objectives T‐cell large granular lymphocytic leukemia (T‐LGLL), reported in up to 58% of inclusion body myositis (IBM) patients, is a rare leukemia of cytotoxic or less commonly helper T cells. The range of myopathies in T‐LGLL and the impact of coexisting T‐LGLL in IBM are not well understood. Our objectives are to investigate the spectrum of
Pannathat Soontrapa +10 more
wiley +1 more source
Whole‐Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies
Annals of Clinical and Translational Neurology, Volume 13, Issue 6, Page 1129-1140, June 2026.ABSTRACT Objective To characterize whole‐body intramuscular fat distribution pattern in patients with sarcoglycanopathies and explore correlations with disease severity, duration and age at onset. Methods Retrospective, cross‐sectional, multicentric study enrolling patients with variants in one of the four sarcoglycan genes who underwent whole‐body ...
Laura Costa‐Comellas +39 more
wiley +1 more source
, 1997 Orbital myositis is a subgroup of the nonspecific inflammatory syndrome or orbital pseudotumor and is characterized by a primary inflammation of extraocular muscles.
Morganho, A +5 more
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ACR Open Rheumatology, Volume 8, Issue 6, June 2026.Objective To characterize longitudinal anti–aminoacyl–tRNA synthetase (anti‐ARS) antibody kinetics in antisynthetase syndrome (ASyS) with isolated organ involvement (IOI) and examine associations with clinical trajectories versus multiple organ involvement (MOI).
Takeshi Suzuki +3 more
wiley +1 more source
Triple-M Overlap Syndrome Associated with Immune Checkpoint Inhibitors: A FAERS Pharmacovigilance Analysis. [PDF]
Healthcare (Basel)Alshamsan B, Ng TL.
europepmc +1 more source
New Spontaneous Model of Fibrodysplasia Ossificans Progressiva
, 2008 We report the first known example of spontaneous, naturally occurring fibrodysplasia ossificans progressiva (FOP) in a mammal. The Southeast Asian mouse deer of the genus _Tragulus_ (Artiodactyla: Tragulidae) have an osseous sheath covering the lower ...
Robert Timm +2 more
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