Magnetic resonance imaging pattern recognition in sporadic Inclusion-Body Myositis
In sporadic inclusion body myositis (IBM), additional tools are needed to confirm the diagnosis, particularly in clinically atypical or pathologically unproven patients. The aims of this study were to refine the pattern of muscle MRI in IBM and to assess
Monforte, Mauro +10 more
core +1 more source
Dilated cardiomyopathy and inclusion body myositis.
Inclusion body myositis (IBM) is the most common inflammatory myopathy after 50 years of age. In contrast to polymyositis and dermatomyositis, in which cardiac involvement is relatively common, current evidences indicate that IBM is not associated with ...
MONDILLO, SERGIO +6 more
core +1 more source
Mitochondrial DNA deletions in inclusion body myositis
Skeletal muscle specimens from three patients with inclusion body myositis, aged 39, 60 and 71 years, respectively, were investigated. Enzyme histochemical staining of cytochrome c oxidase (COX), succinate dehydrogenase and myofibrillar ATPase, and in ...
Larsson, N. +3 more
core
Post‐Filler Complications: Beware of Early Warning Signs of Systemic Diseases
Journal of Cosmetic Dermatology, Volume 25, Issue 7, July 2026.
Hang Wang +4 more
wiley +1 more source
Inclusion Body Myositis in Spring Peepers (Pseudacris Crucifer)
In 2000, 2 adult captive spring peepers ( Pseudacris crucifer) from the same zoological park were humanely euthanized. Histologically, both frogs had degeneration, atrophy, and necrosis of striated myofibers of the tongue admixed with chronic ...
Tim Reichard +4 more
core +1 more source
Acquired adermatoglyphia associated with sporadic inclusion body myositis
A 70-year-old male patient with inclusion body myositis presented to dermatology clinic for evaluation of loss of fingerprints. Eight years previously, he had fingerprints taken for a government permit.
Casterline, Benjamin +8 more
core +1 more source
Proteomic profiles in inclusion body myositis and polymyositis with mitochondrial pathology
Background Idiopathic inflammatory myopathies (IIMs) are autoimmune muscle diseases with distinct clinical, histopathological, and molecular features. Among them, inclusion body myositis (IBM) is refractory to immunotherapy and characterized by combined ...
Felix Kleefeld +22 more
doaj +1 more source
Inclusion body myositis — a case based clinicopathological update
Bodoki Levente +7 more
doaj +1 more source
Myeloid dendritic cell subsets characterise muscle in patients with inclusion body myositis and correlate with the IFN-γ pathway and effector T cell markers. [PDF]
Kirou RA +18 more
europepmc +1 more source
FAIR in practice: minimum metadata schema for bioinformatics analytics by machines. [PDF]
Wijnbergen D +9 more
europepmc +1 more source

