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

Epidemiological and genetic study of exertional rhabdomyolysis in a Warmblood horse family in Switzerland.

Equine veterinary journal - 1 Mar 2011

Johlig L, Valberg S J, Mickelson J R, Klukowska J, Reusser H R, Straub R, Gerber V

Abstract excerpt

REASONS FOR PERFORMING STUDY: Exertional rhabdomyolysis (ER) and its familial basis in Warmblood horses is incompletely understood. OBJECTIVES: To describe the case details, clinical signs and management of ER-affected Warmblood horses from a family with a high prevalence of ER, to determine if histopathological signs of polysaccharide storage myopathy (PSSM) and the glycogen synthase (GYS1) mutation are...

Read the complete abstract on PubMed

Topics

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

Share to Gene Expression Regulation, Enzymologic
Share to Glycogen Synthase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Horse Diseases

Share to Horses

Share to Multivariate Analysis

Share to Physical Conditioning, Animal

Share to Rhabdomyolysis

Share to Switzerland

Source

Identifiers

PMID: 21592222
DOI: 10.1111/j.2042-3306.2010.00161.x

Genes

GYS1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Epidemiological and genetic study of exertional rhabdomyolysis in a Warmblood horse family in Switzerland.PMID 21592222Read ↗

A glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breeds.Semantic proximity Read ↗

Epidemiology of exertional rhabdomyolysis susceptibility in standardbred horses reveals associated risk factors and underlying enhanced performance.Semantic proximity Read ↗

Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breeds.Semantic proximity Read ↗

Polysaccharide storage myopathy phenotype in quarter horse-related breeds is modified by the presence of an RYR1 mutation.Semantic proximity Read ↗

Glycogen synthase 1 (GYS1) mutation in diverse breeds with polysaccharide storage myopathy.Semantic proximity Read ↗

Estimated prevalence of the GYS-1 mutation in healthy Austrian Haflingers.Semantic proximity Read ↗

A GYS1 gene mutation is highly associated with polysaccharide storage myopathy in Cob Normand draught horses.Semantic proximity Read ↗

Presence of the glycogen synthase 1 (GYS1) mutation causing type 1 polysaccharide storage myopathy in continental European draught horse breeds.Semantic proximity Read ↗

Genetic background of the Transylvanian endemic equine recurrent rhabdomyolysis.Semantic proximity Read ↗

Association between population structure and allele frequencies of the glycogen synthase 1 mutation in the Austrian Noriker draft horse.Semantic proximity Read ↗

Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis.Semantic proximity Read ↗

Allele copy number and underlying pathology are associated with subclinical severity in equine type 1 polysaccharide storage myopathy (PSSM1).Semantic proximity Read ↗

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