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Blomqvist, L., & Rieger, I. (1978). Snow leopard references. International Pedigree Book of Snow Leopards, , 153–160.
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Blomqvist, L. (1979). The 1978 register for the captive population of snow leopards, Panthera uncia. International Zoo News, 26(7-8), 17–23.
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Blomqvist, L., & Nystrom, V. (1980). On identifying snow leopards, Panthera uncia, by their facial markings. International Pedigree Book of Snow Leopards, , 159–167.
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Blomqvist, L. (1995). The snow leopard in captivity in 1992. International Zoo News, 42(3), 152–159.
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Bower, J. N. (1983). Shy, elusive, struggling to survive: the snow leopard. The Explorer, , 9–11.
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Brown, J. L., Wasser, S. K., Wildt, D. E., & Graham, L. H. (1994). Steroid Metabolism and the Effectiveness of Fecal Assays for Assessing Reproductive Status in Felids. Biology of Reproduction, 50(suppl 1), 185.
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Chalise, M. K., & Shakya, P. R. (2002). EDITORIAL: Snow Leopard Investigation in Langtang. Nahson Bulletin, 12-13(2002-2003), 1.
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Desch, C. (1993). A new species of hair follicle mite (Acari: Demodecidae) from the snow leopard, Panthera uncia (Schreber, 1775) (Felidae). International Journal of Acarology, 19(1), 63–67.
Abstract: A new species of Demodex is described, in all instars, from the rare and endangered snow leopard, Panthera uncia. This represents only the second demodecid from the family Felidae and the first from a wild cat species. The mite specimens were taken from juvenile hosts raised in captivity. Demodex uncii sp. nov. closely resembles Demodex cati.
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Dexel, B. (2001). Snow leopard conservation: a NABU project in Kyrgyzstan. Oryx, 35(4), 354–355.
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Fix, A. S., Riordan, D. P., Hill, H. T., Gill, M. A., & Evans, M. B. (1989). Feline panleukopena virus and subsequent canine-distemper virus infection in two snow leopards (Panthera uncia). Journal of Zoo and Wildlife Medicine, 20(3), 273–281.
Abstract: Two adult snow leopards (Panthera uncia), male and female, both with vaccinations current, became infected with feline panleukopenia virus (FPV) at the Blank Park Zoo, Des Moines, Iowa, in late 1988. Clinical signs included weakness, hemorrhagic feces, fever, seizures, and nasal discharge. Blood analysis revealed severe lymphopenia and mild anemia. A positive enzyme-linked immunosorbent assay (ELISA) test for FPV on fecal contents from the male leopard confirmed the diagnosis. In spite of intensive therapy, both animals died. Necropsy of the female, which survived for 1 wk after onset of signs, revealed intestinal crypt necrosis, pulmonary consolidation, necrotizing laryngitis, and diffuse lymphoid depletion. The male leopard, which lived 3 wk after onset of illness, had similar enteric and lymphoid lesions. In addition, there was a severe interstitial pneumonia, with syncytial cells containing eosinophilic intracytoplasmic inclusion bodies. Ultrastructural characteristics of these inclusions featured tubular structures consistent with a paramyxovirus. Although repeated virus isolation attempts from the affected lung were negative, polyclonal and monoclonal fluorescent antibody tests were strongly positive for canine distemper virus (CDV). Frozen paired sera from each leopard demonstrated very high acute and convalescing titers to FPV; both animals also seroconverted to CDV, with titers in the male leopard higher than those in the female. Additional tests for toxoplasmosis, feline infectious peritonitis, feline rhinotracheitis, feline calicivirus, feline leukemia, canine parainfluenza, and bovine respiratory syncytial virus were all negative. The neurologic signs present in these leopards remained unexplained, but may have been attributable to CDV infection. A feral cat trapped on zoo property had feces positive for FPV by ELISA. Although the specific contributions of FPV and CDV toward the development of this case are unknown, it is likely that initial FPV-induced immunosuppression allowed the subsequent development of CDV in these snow leopards. The likelihood that initial FPV infection came from feral cats underscores the importance of feral animal control on zoo premises.
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