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6 risultati
Clinical Parelaphostrongylus tenuis infection in two captive American bison (Bison bison).
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METHODS
2 juvenile (17 and 19 months of age) male American bison (Bison bison) were examined because of acute bilateral hind limb weakness and ataxia; 1 animal also had urinary incontinence.
RESULTS
Given the clinical signs and rapid deterioration in the condition of these 2 animals, obtaining a
Parelaphostrongylus tenuis in captive reindeer and sable antelope.
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Parelaphostrongylus tenuis caused neurologic disease in 6 reindeer (Rangifer tarandus tarandus) and 2 sable antelope (Hippotragus niger) that were housed at the National Zoological Park Conservation and Research Center in Front Royal, Va. Progressive hindlimb ataxia and weakness were seen in all
Low-dose meningeal worm (Parelaphostrongylus tenuis) infections in moose (Alces alces).
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Parelaphostrongylosis has a rapid onset and is lethal in neonatal moose (Alces alces) when large numbers of third-stage Parelaphostrongylus tenuis larvae (L3) are given experimentally. Little is known, however, about the severity and prognosis of infections acquired naturally by accidentally
Meningeal worm in experimentally-infected bighorn and domestic sheep.
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In the first (July 1989) of two experiments, each of three bighorn sheep (Ovis canadensis) and three domestic sheep, respectively, was exposed to 25, 150, or 300 infective third-stage larvae (L3) of the meningeal worm, Parelaphostrongylus tenuis. Two bighorn sheep had temporary mild paresis and
Extracting protostrongylid nematode larvae from ungulate feces.
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A major weakness of the Baermann funnel technique for extracting nematode larvae from feces is the funnel. As many as 67% of Parelaphostrongylus tenuis first-stage larvae lodged on the sloping surface of glass Baermann funnels. The number of larvae collected after 24 hr was not significantly
A double-blind, controlled evaluation of the value of sarapin in neural blockade.
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OBJECTIVE
To demonstrate the effectiveness of Sarapin in prolonging the action of neural blockade with improved pain relief.
METHODS
Prospective, continuous, double-blind trial including 500 consecutive patients undergoing either caudal epidural injections; cervical, thoracic, lumbosacral facet
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