A lysosomal storage disease of Romney sheep that resembles human type 3 GM1 gangliosidosis

Acta Neuropathologica

Volumn 101, Issue 3, 2001, Pages 225-228

  Ryder, S J ^a   Simmons, M M ^a  

^a VETERINARY LABORATORIES AGENCY   (United Kingdom)

Author keywords

Gangliosidosis GM1; Ovine lysosomal storage disease

Indexed keywords

GLYCOLIPID;

ANIMAL DISEASE; ANIMAL TISSUE; ANIMAL WELFARE; ARTICLE; BRAIN NERVE CELL; BRAIN TISSUE; CELL GRANULE; CELL ULTRASTRUCTURE; CONTROLLED STUDY; CORPUS STRIATUM; EOSINOPHILIA; FEMALE; GM1 GANGLIOSIDOSIS; HEALTH SURVEY; LYSOSOME STORAGE DISEASE; NERVE CELL MEMBRANE; NEUROPATHOLOGY; NONHUMAN; PERIKARYON; PRIORITY JOURNAL; SCRAPIE; SHEEP;

EID: 0035109239     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004010000267     Document Type: Article

References (13)

1. M1 gangliosidosis presenting as dystonia. I. Clinical and pathological features
2. Observations on diseases of the central nervous system of sheep in New Zealand
3. Lysosomal storage diseases in livestock
4. Inherited lysosomal storage diseases: An essay in comparative medicine
5. Lysosomal and peroxisomal disorders
6. M1-gangliosidosis
7. Lectin histochemistry of an ovine lysosomal storage disease with deficiencies of β-galactosidase and α-neuraminidase
8. The lesions of an ovine lysosomal storage disease: Initial characterization
9. Ovine GM1 gangliosidosis
10. Chronic GM1 Gangliosidosis presenting as dystonia: Clinical and biochemical studies in a new case
11. M1-gangliosidosis
12. Veterinary Neuropathology
13. Type 3 GM1 gangliosidosis: Characteristic MRI findings correlated with dystonia