Inclusion body myositis: a distinct variety of idiopathic inflammatory myopathy.
about
Treatment for inclusion body myositisTreatment for inclusion body myositisSarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositisInflammation induced loss of skeletal muscleCylindrical spirals in human skeletal muscleCylindrical spirals in a familial neuromuscular disorderNature of "Tau" immunoreactivity in normal myonuclei and inclusion body myositis.Polymyositis/dermatomyositis: the current positionInclusion body myositis: an underdiagnosed condition?Cyclosporin in the management of polymyositis and dermatomyositisInclusion body myositis: a case with associated collagen vascular disease responding to treatmentDysphagia in inclusion body myositis.Impaired autophagy in sporadic inclusion-body myositis and in endoplasmic reticulum stress-provoked cultured human muscle fibersTheories of the pathogenesis of inclusion body myositis.Inclusion body myositis and myopathies.Safety and efficacy of strength training in patients with sporadic inclusion body myositis.An overview of polymyositis and dermatomyositis.An expanded cortical representation for hand movement after peripheral motor denervationIncreased capillaries in mitochondrial myopathy: implications for the regulation of oxygen delivery.The concomitant occurrence of Sjögren's syndrome and polymyositis.The role of quantitative electromyography in inclusion body myositisA rare association of early-onset inclusion body myositis, rheumatoid arthritis and autoimmune thyroiditis: a case report and literature review.Sporadic inclusion body myositis: pathogenic considerations.Malignancy is associated with dermatomyositis but not polymyositis in Northern New England, USA.Vascular involvement in the pathogenesis of idiopathic inflammatory myopathies.Idiopathic inflammatory myopathies: diagnostic criteria, classification and epidemiological features.Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkersIntegrated classification of inflammatory myopathies.Clinical assessment determines the diagnosis of inclusion body myositis independently of pathological features.Morphological observations in skeletal muscle from patients with a mitochondrial myopathy.Inflammatory myopathy: a review of etiologic and pathogenetic factors.Inclusion body myositis and renal cell carcinoma. Report of two cases and review of the literature.Mitochondrial genome: defects, disease, and evolution.Inclusion body myositis: the mumps virus hypothesis.Sporadic distal myopathy with early adult onset.Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis.Conspicuous accumulation of a single-stranded DNA binding protein in skeletal muscle fibers in inclusion body myositisInclusion-body myositis: clinicopathological studies and isolation of an adenovirus type 2 from muscle biopsy specimen.Subacute skeletal myopathy induced by 2,4-dichlorophenoxyacetate in rats and guinea pigs.Adult-onset autosomal dominant limb-girdle muscular dystrophy.
P2860
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P2860
Inclusion body myositis: a distinct variety of idiopathic inflammatory myopathy.
description
1978 nî lūn-bûn
@nan
1978年の論文
@ja
1978年学术文章
@wuu
1978年学术文章
@zh-cn
1978年学术文章
@zh-hans
1978年学术文章
@zh-my
1978年学术文章
@zh-sg
1978年學術文章
@yue
1978年學術文章
@zh
1978年學術文章
@zh-hant
name
Inclusion body myositis: a distinct variety of idiopathic inflammatory myopathy.
@en
type
label
Inclusion body myositis: a distinct variety of idiopathic inflammatory myopathy.
@en
prefLabel
Inclusion body myositis: a distinct variety of idiopathic inflammatory myopathy.
@en
P2093
P356
P1433
P1476
Inclusion body myositis: a distinct variety of idiopathic inflammatory myopathy.
@en
P2093
P356
10.1212/WNL.28.1.8
P407
P577
1978-01-01T00:00:00Z