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Jitender Bhandal Alan Kuzma Greg Starrak 《The Canadian veterinary journal. La revue veterinaire canadienne》2008,49(10):1002-1004
The abdominal ultrasonogram of a dog admitted for acute onset of collapse revealed an abnormally displaced left medial liver lobe with no blood flow. Surgical and histological findings confirmed the ultrasonographic diagnosis of left liver lobe torsion. Ultrasonographic findings were useful and probably sufficient for a correct diagnosis. 相似文献
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Anderson GM Lewis DD Radasch RM Marcellin-Little DJ Degna MT Cross AR 《Journal of the American Animal Hospital Association》2003,39(5):479-498
Fracture stabilization using circular external skeletal fixation was evaluated in 14 dogs with antebrachial fractures and 11 dogs with crural fractures. Most dogs were consistently weight bearing on the stabilized limb by 3 days following surgery. Although all dogs developed minor wire/pin tract inflammation and eight dogs developed major wire/pin tract inflammation, postoperative lameness was not consistently associated with wire/pin tract complications. Fractures in 23 dogs achieved radiographic union (mean +/- standard deviation [SD], 61 +/- 21 days; median, 57 days) without additional surgery; two dogs required restabilization of their fractures with linear fixators. Twenty of the 21 owners that could be contacted felt their dog had no (n=15) or only a mild (n=5) intermittent lameness at the time of final, long-term (mean +/- SD, 37 +/- 17 months; median, 42 months) assessment. 相似文献
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Transmissible spongiform encephalopathies (TSEs) or prion diseases are unique disorders that are not caused by infectious micro-organisms (bacteria or fungi), viruses or parasites, but rather seem to be the result of an infectious protein. TSEs are comprised of fatal neurodegenerative disorders affecting both human and animals. Prion diseases cause sponge-like degeneration of neuronal tissue and include (among others) Creutzfeldt–Jacob disease in humans, bovine spongiform encephalopathy (BSE) in cattle and scrapie in sheep. TSEs are characterized by the formation and accumulation of transmissible (infectious) disease-associated protease-resistant prion protein (PrPSc), mainly in tissues of the central nervous system. The exact molecular processes behind the conversion of PrPC into PrPSc are not clearly understood. Correlations between prion protein polymorphisms and disease have been found, however in what way these polymorphisms influence the conversion processes remains an enigma; is stabilization or destabilization of the prion protein the basis for a higher conversion propensity? Apart from the disease-associated polymorphisms of the prion protein, the molecular processes underlying conversion are not understood. There are some notions as to which regions of the prion protein are involved in refolding of PrPC into PrPSc and where the most drastic structural changes take place. Direct interactions between PrPC molecules and/or PrPSc are likely at the basis of conversion, however which specific amino acid domains are involved and to what extent these domains contribute to conversion resistance/sensitivity of the prion protein or the species barrier is still unknown. 相似文献
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Sainz-Sánchez Pedro Alan López-González Felipe Estrada-Flores Julieta Gertrudis Martínez-García Carlos Galdino Arriaga-Jordán Carlos Manuel 《Tropical animal health and production》2017,49(1):179-186
Tropical Animal Health and Production - The use and management of native grassland for dairy production during the rainy season was studied on two small-scale dairy farms in the highlands of... 相似文献