Results 121 to 130 of about 15,582 (230)
Strenuous exercise induces transient, region‐specific neurochemical changes in the human brain. Dynamic proton magnetic resonance spectroscopy (1H‐MRS) and spectroscopic imaging (1H‐MRSI) revealed reductions in total creatine (tCr), and elevations in glutamate/glutamine (Glx), and lactate (Lac) in frontal and parietal brain regions.
Jedd Pratt +6 more
wiley +1 more source
Neurological complications of immune checkpoint inhibitors: what happens when you \u27take the brakes off\u27 the immune system. [PDF]
Patients with advanced malignancies treated with immune checkpoint inhibitors are at increased risk for developing immune-related neurological complications.
Dalakas, Marinos
core +1 more source
Interrelation of inflammation and APP in sIBM: IL-1 beta induces accumulation of beta-amyloid in skeletal muscle. [PDF]
Distinct interrelationships between inflammation and beta-amyloid-associated degeneration, the two major hallmarks of the skeletal muscle pathology in sporadic inclusion body myositis (sIBM), have remained elusive.
Barthel, Konstanze +5 more
core +1 more source
Capabilities of magnetic resonance imaging in the diagnosis of idiopathic inflammatory myopathies
Idiopathic inflammatory myopathies (IIM) are a group of chronic autoimmune conditions characterized by proximal muscle weakness and potentially accompanied by a range of extramuscular clinical manifestations.
A. A. Kolomeychuk
doaj +1 more source
Determining the Characteristic Vocabulary for a Specialized Dictionary using Word2vec and a Directed Crawler [PDF]
Specialized dictionaries are used to understand concepts in specific domains, especially where those concepts are not part of the general vocabulary, or having meanings that differ from ordinary languages.
Grefenstette, Gregory, Muchemi, Lawrence
core +3 more sources
Multi-omics analysis in inclusion body myositis identifies mir-16 responsible for HLA overexpression
Background Inclusion Body Myositis is an acquired muscle disease. Its pathogenesis is unclear due to the co-existence of inflammation, muscle degeneration and mitochondrial dysfunction.
Daphne Wijnbergen +9 more
doaj +1 more source
Desmin forms toxic, seeding-competent amyloid aggregates that persist in muscle fibers [PDF]
Desmin-associated myofibrillar myopathy (MFM) has pathologic similarities to neurodegeneration-associated protein aggregate diseases. Desmin is an abundant muscle-specific intermediate filament, and disease mutations lead to its aggregation in cells ...
Arhzaouy, Khalid +6 more
core +1 more source
Inclusion body myositis — a case based clinicopathological update
Bodoki Levente +7 more
doaj +1 more source

