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

Inclusion body myositis coexisting with hypertrophic cardiomyopathy: an autopsy study.

Neuromuscular disorders : NMD - 1 Aug 2012

Inamori Yukie, Higuchi Itsuro, Inoue Teruhiko, Sakiyama Yusuke, Hashiguchi Akihiro, Higashi Keiko, Shiraishi Tadafumi, Okubo Ryuichi, Arimura Kimiyoshi, Mitsuyama Yoshio, Takashima Hiroshi

Abstract excerpt

Inclusion body myositis is an inflammatory myopathy characterized pathologically by rimmed vacuoles and the accumulation of amyloid-related proteins. Autopsy studies in these patients, including histochemical examinations of multiple skeletal muscles, have not yet been published. In this paper, we describe the autopsy findings of a patient with inclusion body myositis and hypertrophic cardiomyopathy. A...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Autopsy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cardiomyopathy, Hypertrophic

Share to Carrier Proteins

Share to Comorbidity

Share to Muscle, Skeletal

Share to Myocardium

Share to Myositis, Inclusion Body

Source

Identifiers

PMID: 22560514
DOI: 10.1016/j.nmd.2012.03.011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inclusion body myositis coexisting with hypertrophic cardiomyopathy: an autopsy study.PMID 22560514Read ↗

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

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

Molecular pathology and pathogenesis of inclusion-body myositis.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 ↗

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

A case of progressive quadriceps weakness and elevated creatine kinase level mimicking inclusion body myositis.Semantic proximity Read ↗

Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesisSemantic proximity Read ↗

Proteomic Analysis of Inclusion Body MyositisSemantic proximity Read ↗

Mitochondrial pathology in inclusion body myositisSemantic proximity Read ↗

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia.Semantic proximity Read ↗

Immune and myodegenerative pathomechanisms in inclusion body myositisSemantic proximity Read ↗

The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews.Semantic proximity Read ↗

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