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

Hemolysis, myopathy, and cardiac disease associated with hereditary phosphofructokinase deficiency in two Whippets.

Veterinary clinical pathology - 1 Mar 2009

Gerber Karen, Harvey John W, D'Agorne Sara, Wood Jonathan, Giger Urs

Abstract excerpt

Two male castrated Whippet littermates were presented at 1 year of age for pallor, tachycardia, systolic heart murmur, dark yellow to orange feces, intermittent lethargy, pigmenturia, and muscle shivering or cramping after exercise. Persistent macrocytic hypochromic anemia with marked reticulocytosis and metarubricytosis was found when CBC results were compared with reference values for Whippets. Increased serum...

Read the complete abstract on PubMed

Topics

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

Share to Dog Diseases
Share to Dogs
Share to Erythrocytes

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Heart Diseases

Share to Hemolysis

Share to Muscular Diseases

Source

Open in PubMed Open full text

Identifiers

PMID: 19228357
DOI: 10.1111/j.1939-165X.2008.00089.x
PMCID: PMC2692053

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hemolysis, myopathy, and cardiac disease associated with hereditary phosphofructokinase deficiency in two Whippets.PMID 19228357Read ↗

Hereditary phosphofructokinase deficiency in wachtelhunds.Semantic proximity Read ↗

Inherited phosphofructokinase deficiency in an American cocker spaniel.Semantic proximity Read ↗

Clinical, metabolic, and molecular genetic characterization of hereditary methemoglobinemia caused by cytochrome b5 reductase deficiency in 30 dogs.Semantic proximity Read ↗

Myotonia congenita in a Jack Russell terrier.Semantic proximity Read ↗

Erythrocytic pyruvate kinase mutations causing hemolytic anemia, osteosclerosis, and secondary hemochromatosis in dogs.Semantic proximity Read ↗

Other erythrocyte enzyme deficiencies associated with non-haematological symptoms: phosphoglycerate kinase and phosphofructokinase deficiency.Semantic proximity Read ↗

Idiopathic Asymptomatic Thrombocytopenia in Cavalier King Charles Spaniels Is an Autosomal Recessive TraitSemantic proximity Read ↗

Transient hyperlipidemia in a litter of kittens.Semantic proximity Read ↗

Systemic calcinosis in a Quarter Horse gelding homozygous for a myosin heavy chain 1 mutation.Semantic proximity Read ↗

Idiopathic Asymptomatic Thrombocytopenia in Cavalier King Charles Spaniels Is an Autosomal Recessive TraitSemantic proximity Read ↗

Haemostatic, fibrinolytic and inflammatory profiles in West Highland white terriers with canine idiopathic pulmonary fibrosis and controls.Semantic proximity Read ↗

Clinical and biochemical signs in Fleckvieh cattle with genetically confirmed Fanconi-Bickel syndrome (cattle homozygous for Fleckvieh haplotype 2).Semantic proximity Read ↗

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