Zobrazeno 1 - 8
of 8
pro vyhledávání: '"R. D. Murnane"'
Publikováno v:
Veterinary Pathology. 28:332-335
Lysosom al storage diseases are caused by inherited defigangliosidos is has recentl y been characterized." A comparciencies of vario us lysosomal enzymes and result in the proati ve study oflectin bind ing pattern s was per formed on cengress ive sto
Publikováno v:
Journal of zoo and wildlife medicine : official publication of the American Association of Zoo Veterinarians. 29(2)
Nine small cats, including one bobcat (Felis rufus), one Pallas cat (F. manul), one Canada lynx (F. lynx canadensis), two fishing cats (F. viverrina), two margays (F. wiedii), and two sand cats (F. margarita), necropsied between June 1995 and March 1
Publikováno v:
Journal of zoo and wildlife medicine : official publication of the American Association of Zoo Veterinarians. 28(4)
An adult male mountain chameleon (Chameleo montium), one of 92 individuals recently caught in the wild and transported, died after a 28-day history of anorexia. Gross examination revealed marked emaciation and enteric nematodiasis. Histopathologic ex
Publikováno v:
The American journal of pathology. 139(6)
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 4(6)
Ovine GM1 gangliosidosis, an inherited disease of sheep with deficiencies of beta-galactosidase and alpha-neuraminidase, storage of GM1 ganglioside, asialo-GM1 and neutral long chain oligosaccharides in the brain, autosomal recessive inheritance, and
Publikováno v:
Equine Veterinary Journal. 19:552-555
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology. 52(2)
This study reports the quantitative changes in the pulmonary proximal acinar region following chronic exposure to diesel exhaust and following an additional 6 months in clean air. Cats (13 months of age) from a minimum disease colony were exposed to
Publikováno v:
The American journal of pathology. 134(2)
An inherited disease associated with deficiencies of beta-galactosidase and alpha-neuraminidase has been identified recently in sheep. The clinical signs, the deficiency of lysosomal enzymes, and the familial nature of the disorder suggested that the