Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesis

1 Nov 1998

Abstract excerpt

We discuss the pathologic diagnostic criteria and review the major new advances related to seeking the pathogenic mechanism of sporadic inclusion-body myositis (s-IBM) and hereditary inclusion-body myopathy (h-IBM). A classification of the various h-IBM syndromes is also presented. The several forms of the h-IBMs have different genetic transmissions and probably different genetic defects. In neither s-IBM nor the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cardiomyopathy and Myosin Studies
Share to Eosinophilic Disorders and Syndromes
Share to Inflammatory Myopathies and Dermatomyositis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 9812213
DOI: 10.1097/00002281-199811000-00005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesisPMID 9812213Read ↗

Inclusion-body myositis and myopathies: different etiologies, possibly similar pathogenic mechanisms.Semantic proximity Read ↗

Inclusion-Body Myositis: Newest Concepts of Pathogenesis and Relation to Aging and Alzheimer DiseaseSemantic proximity Read ↗

Molecular pathology and pathogenesis of inclusion-body myositis.Semantic proximity Read ↗

New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathiesSemantic proximity Read ↗

Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagySemantic proximity Read ↗

Newest pathogenetic considerations in inclusion-body myositis: possible role of amyloid-beta, cholesterol, relation to aging and to Alzheimer's disease.Semantic proximity Read ↗

Inclusion-body myositis: muscle-fiber molecular pathology and possible pathogenic significance of its similarity to Alzheimer’s and Parkinson’s disease brainsSemantic proximity Read ↗

Proposed pathogenetic cascade of inclusion-body myositis: importance of amyloid-beta, misfolded proteins, predisposing genes, and aging.Semantic proximity Read ↗

Sporadic Inclusion Body Myositis at the Crossroad between Muscle Degeneration, Inflammation and AgingSemantic proximity Read ↗

Inclusion-body myositis: a myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition.Semantic proximity Read ↗

Sporadic inclusion-body myositis: a proposed key pathogenetic role of the abnormalities of the ubiquitin-proteasome system, and protein misfolding and aggregation.Semantic proximity Read ↗

Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with ExtrasSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.