Zobrazeno 1 - 10
of 72
pro vyhledávání: '"C. R. Huxtable"'
Autor:
C. R. Huxtable, D. H. Slatter
Publikováno v:
Equine Veterinary Journal. 15:98-100
Publikováno v:
Australian Veterinary Journal. 77:361-366
The prevalence, mode of inheritance and urinalysis findings in Bull Terriers with polycystic kidney disease were assessed by screening 150 clinically normal dogs. The disorder was diagnosed in 39 dogs on the basis of renal ultrasound results and fami
Publikováno v:
Australian Veterinary Journal. 76:733-737
A 5-month-old female Rottweiler dog was diagnosed to have a neurodegenerative disease that has been recently report ed in Rottweilers from North America and Europe. The dog was presented with progressive signs of ataxia, tetraparesis and inspiratory
Publikováno v:
Australian Veterinary Journal. 75:20-23
Publikováno v:
Australian Veterinary Journal. 79:679-681
Focal intramural nodules were palpated in the rectal wall of a 12-year-old pony mare presented for rectal prolapse. Eosinophilic proctitis was diagnosed by examination of fine needle aspirates and biopsy of the largest rectal nodule. After treatment
Publikováno v:
Veterinary Pathology. 37:483-485
Marginal siderosis is recognized in humans as an uncommon clinicopathologic entity characterized by degeneration of neural tissue at the surface of the brain and spinal cord, in association with the accumulation of hemosiderin, and resulting from chr
Autor:
Wayne F. Robinson, M. A. B. Thomas, Jennifer Hood, L. James, C. R. Huxtable, R.J. Sutherland, W. T. Clark
Publikováno v:
Journal of Small Animal Practice. 32:241-248
A group of non‐azotaemic bull terriers from families with hereditary nephritis had significant subclinical renal disease. Of the renal function tests carried out, proteinuria, almost exclusively albumin, was a reliable and early indicator of glomer
Publikováno v:
Research in Veterinary Science. 49:177-181
Brain tissue from 33 dogs with non-suppurative encephalitis was examined for evidence of canine distemper virus (CDV) encephalitis. Sections were examined for lesions, inclusion bodies, syncytial cells and CDV antigen using a double bridge unlabelled
Publikováno v:
Scopus-Elsevier
Background. Autosomal dominant Alport syndrome is a rare inherited disease characterized clinically by haematuria, renal failure and deafness, and ultrastructurally by a lamellated glomerular basement membrane (GBM). It is usually caused by mutations