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

MODERN ASPECTS OF ETIOPATHOGENESIS, DIAGNOSIS, CLINICAL COURSE AND TREATMENT OF SPORADIC INCLUSION BODY MYOSITIS.

Georgian medical news - 1 Jan 2020

Shakarishvili R, Kvirkvelia N, Nikolaishvili I, Nebadze E

Abstract excerpt

While it is the most common inflammatory myopathy among middle-aged and elderly people, sporadic inclusion body myositis (IBM) presents as the most challenging disease to diagnose. The prevalence of IBM varies greatly depending on geographical, ethnic and age factors. Frequency of the disease incidence among the general population ranges from 1:1,000,000 to 1:14,000. Over the past 50 years, it has tripled. The...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Aged
Share to Algorithms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Muscle, Skeletal

Share to Myositis, Inclusion Body

Source

Identifiers

PMID: 32141855

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

MODERN ASPECTS OF ETIOPATHOGENESIS, DIAGNOSIS, CLINICAL COURSE AND TREATMENT OF SPORADIC INCLUSION BODY MYOSITIS.PMID 32141855Read ↗

Inclusion body myositis: A review of clinical and genetic aspects, diagnostic criteria and therapeutic approachesSemantic proximity Read ↗

Sporadic inclusion body myositis: the genetic contributions to the pathogenesisSemantic proximity Read ↗

Idiopathic inflammatory myopathies: current trends in pathogenesis, clinical features, and up-to-date treatment recommendations.Semantic proximity Read ↗

Inclusion body myositis: from genetics to clinical trialsSemantic proximity Read ↗

Deciphering the clinical presentations, pathogenesis, and treatment of the idiopathic inflammatory myopathies.Semantic proximity Read ↗

Clinical heterogeneity based on race and sex within a large cohort of inclusion body myositis patientsSemantic proximity Read ↗

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

Juvenile idiopathic inflammatory myositis: an update on pathophysiology and clinical care.Semantic proximity Read ↗

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

Idiopathic inflammatory myopathies: epidemiology, classification, and diagnostic criteriaSemantic proximity Read ↗

Inclusion Body MyositisSemantic proximity Read ↗

Idiopathic inflammatory myopathies: diagnostic criteria, classification and epidemiological features.Semantic proximity Read ↗

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