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Abstract

This article discussed the clinical aspects, prevalence, and risk factors of brachycephalic obstructive airway syndrome (BOAS) in brachycephalic dog breeds and highlights the two different methods to assess airway function in these breeds, a functional grading system which is based on listening to...

Author(s)
Ladlow, J.; Liu NaiChieh; Kalmar, L.; Sargan, D.
Publisher
BMJ Publishing Group, London, UK
Citation
Veterinary Record, 2018, 182, 13, pp 375-378
Abstract

Background: The merle colour in dogs (merle: blackbird) is caused by a retrotransposon insertion in the SILV gene, resulting in malfunction in the eumelanin producing pigment cells. In homozygous (MM) individuals congenital auditory and ophthalmologic disorders are common, therefore the mating of...

Author(s)
Pelles, Z.; Maróti-Agóts, Á.; Gáspárdy, A.; Zöldág, L.; Zenke, P.
Publisher
Herman Ottó Institute Nonprofit Ltd., Budapest, Hungary
Citation
Magyar Állatorvosok Lapja, 2018, 140, 2, pp 121-127
Abstract

Author(s)
Gough, A.
Publisher
Veterinary Business Development Ltd, Peterborough, UK
Citation
Veterinary Times, 2017, 47, 21, pp 23
Abstract

Genetic diseases occur in breeds used for law enforcement. As important team members, dogs are expected to operate at peak performance for several years and are significant investments for both the initial purchase and extensive, specialized training. Previous studies have not focused on causes for ...

Author(s)
Shaffer, L. G.; Ramirez, C. J.; Phelps, P.; Aviram, M.; Walczak, M.; Bar-Gal, G. K.; Ballif, B. C.
Publisher
S Karger AG, Basel, Switzerland
Citation
Cytogenetic and Genome Research, 2017, 153, 4, pp 198-204
Abstract

A 3-year-old, female Greater Swiss Mountain dog developed a hemoperitoneum following an exploratory laparotomy and ovariohysterectomy. Platelet count, PT, APTT, and plasma von Willebrand factor antigen concentration were within RIs. A buccal mucosal bleeding time (BMBT) was prolonged. Given the...

Author(s)
Flores, R. S.; Boudreaux, M. K.; Vasquez, B.; Bristow, P.; Aronson, L. R.; Santoro-Beer, K.; Callan, M. B.
Publisher
Wiley, Boston, USA
Citation
Veterinary Clinical Pathology, 2017, 46, 4, pp 569-574
Abstract

Background: Molecular genetics has made significant advances in the analysis of hereditary dermatoses during the last several years. Objectives: To provide an update on currently available genetic tests for skin diseases of dogs, cats and horses, and to aid the veterinary clinician in the...

Author(s)
Leeb, T.; Müller, E. J.; Roosje, P.; Welle, M.
Publisher
Wiley, Oxford, UK
Citation
Veterinary Dermatology, 2017, 28, 1, pp e1
Abstract

Animals that have inherited a mutant gene from their parents (father and/or mother) may acquire hereditary diseases. Most mutations are autosomal recessive. Usually, hereditary diseases go unnoticed until symptoms arise. The objective of this study is to screen four canine hereditary diseases in...

Author(s)
Kuo RueiJia; Liu ChenHsuan; Hsieh ChinFong; Jiang JiaWei; Liao TaiChing [Liao, T. C. A. ]
Publisher
Chinese Society of Veterinary Science, Taipei, Taiwan
Citation
Taiwan Veterinary Journal, 2017, 43, 4, pp 277-284
Abstract

Objective: To develop a method to rapidly screen candidate genes for association with recessively inherited progressive retinal atrophy (PRA) in pedigrees of dog in which a causative mutation has not been identified. Animal studied: Thirteen PRA-affected dogs were used in this study. Procedures:...

Author(s)
Winkler, P. A.; Davis, J. A.; Petersen-Jones, S. M.; Venta, P. J.; Bartoe, J. T.
Publisher
Wiley, Boston, USA
Citation
Veterinary Ophthalmology, 2017, 20, 4, pp 372-376
Abstract

Background: Spinocerebellar ataxia also referred to as hereditary ataxia comprises different forms of progressive neurodegenerative diseases. A complex mode of inheritance was most likely in Parson Russell Terriers (PRT) and in Jack Russell Terriers (JRT). Recently, the missense mutation ...

Author(s)
Gast, A. C.; Metzger, J.; Tipold, A.; Distl, O.
Publisher
BioMed Central Ltd, London, UK
Citation
BMC Veterinary Research, 2016, 12, 225, pp (10 October 2016)
Abstract

Identification of genetic mutations causing disease is helpful in breeding programmes aimed at enhancing the qualities of a breed. The ceský fousek (CF), also known as the Bohemian wirehaired pointing griffon, is a versatile hunting dog that dates back to the 14th century. Because no genetic...

Author(s)
Shaffer, L. G.; Ramirez, C. J.; Sundin, K.; Connell, L. B.; Ballif, B. C.
Publisher
BMJ Publishing Group, London, UK
Citation
Veterinary Record Case Reports, 2016, 4, 2, pp e000346

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