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Electromyography varies by stage in inclusion body myositis [PDF]

open access: yesFrontiers in Neurology, 2023
IntroductionInclusion body myositis (IBM) is a chronic inflammatory muscle disease that is characterized by mixed myogenic and neurogenic electromyography (EMG) findings.
Tomoo Mano   +7 more
doaj   +2 more sources

Obturator hernia associated with inclusion body myositis: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Inclusion body myositis is a progressive muscle disease characterized by weakness, specifically in the flexor digitorum profundus and quadriceps muscles, and commonly affects men over 50 years of age.
Yuma Sato   +3 more
doaj   +2 more sources

Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with Extras [PDF]

open access: yesBiomolecules, 2019
The sporadic form of inclusion body myositis (IBM) is the most common late-onset myopathy. Its complex pathogenesis includes degenerative, inflammatory and mitochondrial aspects.
Boel De Paepe
doaj   +3 more sources

Inclusion body myositis in an older patient following a fall [PDF]

open access: yesClinical Case Reports, 2023
Key Clinical Message After experiencing a fall, an 82‐year‐old woman developed progressive loss of lower limb strength and was diagnosed with inclusion body myositis.
Haruma Saiki   +5 more
doaj   +2 more sources

Mitochondrial defects in sporadic inclusion body myositis—causes and consequences [PDF]

open access: yesFrontiers in Cell and Developmental Biology
Sporadic inclusion body myositis (sIBM) is a distinct subcategory of Idiopathic Inflammatory Myopathies (IIM), characterized by unique pathological features such as muscle inflammation, rimmed vacuoles, and protein aggregation within the myofibers ...
Elsie Chit Yu Iu, Ho So, Chi Bun Chan
doaj   +2 more sources

Multi-omics analysis in inclusion body myositis identifies mir-16 responsible for HLA overexpression [PDF]

open access: yesOrphanet Journal of Rare Diseases
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   +2 more sources

Inclusion Body Myositis [PDF]

open access: yesNeurologic Clinics, 2012
The idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of rare disorders that share many similarities. In addition to sporadic inclusion body myositis (IBM), these include dermatomyositis, polymyositis, and autoimmune necrotizing myopathy. IBM is the most common IIM after age 50 years.
Mazen M, Dimachkie, Richard J, Barohn
  +9 more sources

Inclusion body myositis [PDF]

open access: yesCurrent Opinion in Rheumatology, 2002
Inclusion body myositis (IBM) is an inflammatory myopathy with distinctive clinicopathologic features. The etiology of IBM remains elusive. The immune-mediated basis for this disease has been challenged by evidence implicating a number of divergent etiologic factors.
Rabi, Tawil, Robert C, Griggs
openaire   +4 more sources

Increasing daily duration of rehabilitation for inpatients with sporadic inclusion body myositis may contribute to improvement in activities of daily living: A nationwide database cohort study

open access: yesJournal of Rehabilitation Medicine, 2023
Objective: To analyse the association between the daily duration of rehabilitation for inpatients with sporadic inclusion body myositis and improvement in activities of daily living, using a Japanese nationwide inpatient administrative claims database ...
Takuaki Tani   +2 more
doaj   +1 more source

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