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

CAPN3 mutations in patients with idiopathic eosinophilic myositis.

Annals of neurology - 1 Jun 2006

Krahn Martin, Lopez de Munain Adolfo, Streichenberger Nathalie, Bernard Rafaëlle, Pécheux Christophe, Testard Hervé, Pena-Segura José L, Yoldi Eugenia, Cabello Ana, Romero Norma B, Poza Juan J, Bouillot-Eimer Sandrine, Ferrer Xavier, Goicoechea Maria, Garcia-Bragado Federico, Leturcq France, Urtizberea J Andoni, Lévy Nicolas

Abstract excerpt

OBJECTIVE: Eosinophilic myositis (EM) constitutes a rare pathological entity characterized by eosinophilic infiltration of skeletal muscles, usually associated with parasite infections, systemic disorders, or the intake of drugs or L-tryptophan. The exclusion of such causes defines the spectrum of idiopathic EM. Based on a protein analysis performed in one affected patient, we identified the gene encoding...

Read the complete abstract on PubMed

Topics

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

Share to Blotting, Western
Share to Calpain

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Creatine Kinase

Share to Eosinophilia

Share to Immunohistochemistry

Share to Muscle Proteins

Share to Myositis

Source

Identifiers

PMID: 16607617
DOI: 10.1002/ana.20833

Genes

CAPN3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

CAPN3 mutations in patients with idiopathic eosinophilic myositis.PMID 16607617Read ↗

ADULTS WITH EOSINOPHILIC MYOSITIS AND CALPAIN-3 MUTATIONSSemantic proximity Read ↗

Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy?Semantic proximity Read ↗

Identification of novel pathogenic variants of Calpain-3 gene in limb girdle muscular dystrophy R1.Semantic proximity Read ↗

CAPN3: A muscle‑specific calpain with an important role in the pathogenesis of diseases (Review)Semantic proximity Read ↗

A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort.Semantic proximity Read ↗

Mutational Spectrum of CAPN3 with Genotype-Phenotype Correlations in Limb Girdle Muscular Dystrophy Type 2A/R1 (LGMD2A/LGMDR1) Patients in India.Semantic proximity Read ↗

Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations.Semantic proximity Read ↗

Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decay.Semantic proximity Read ↗

Experiences in the molecular genetic and histopathological evaluation of calpainopathies.Semantic proximity Read ↗

Calpainopathy-a survey of mutations and polymorphisms.Semantic proximity Read ↗

Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes.Semantic proximity Read ↗

Molecular diagnosis in LGMD2A: mutation analysis or protein testing?Semantic proximity Read ↗

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