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Biomedical subjects

J B Tasker

Publications and source records attributed to J B Tasker.

At least 19 recordsLinked to original sources
PubMed1985

Chronic active hepatitis in 26 Doberman pinschers.

Chronic active hepatitis with increased hepatic copper concentration was diagnosed in 25 female and 1 male Doberman Pinscher dogs. Common clinical signs included polyuria/polydipsia, weight loss, anorexia, icterus, and ascites. Increased liver enzyme activities and abnormal liver function test results were the most consistent clinicopathologic changes. The dogs were assigned to 3 groups on the basis of clinical course of the disease. Group 1 dogs (n = 12) had clinical signs of advanced liver failure and died within one week. Group 2 dogs (n = 7) had less severe clinical signs of liver disease and died within one month. Group 3 dogs (n = 5) did not have clinical signs of illness or had mild clinical signs of liver disease and died 1 to 42 months after initial evaluation. One dog could not be reevaluated and another dog was alive 3 months after initial examination. Treatments consisted of supportive care for dogs in group 1, and dietary manipulations and corticosteroids for dogs in groups 2 and 3. The association of increased liver copper concentration and chronic active hepatitis is not known.

Animals↗
PubMed1979

Lymphoreticular neoplasia in a dog resembling malignant histiocytosis (histiocytic medullary reticulosis) in man.

Malignant histiocytosis was diagnosed in a 4-year-old-dog. Major clinicopathologic findings included multiple cutaneous tumors, peripheral lymphadenopathy, hepatomegaly, lytic bone lesions, anemia, thrombocytopenia, and monoclonal IgA gammopathy. Pathologic findings included multi-systemic infiltration of erythrophagocytic malignant histiocytes. Chemotherapy was unsuccessful.

Animals↗
PubMed1978

Studies on the use of Coulter Chemistry in the veterinary laboratory: day-to day reproducibility and the effects of storage, hemolysis, lipemia, hyperbilirubinemia and anticoagulants on test results.

A study was done to determine the variations in clinical chemistry test results that might be due to day-to-day changes in laboratory testing conditions or to variations in specimens submitted. Laboratory precision and specimen storage conditions had relatively little effect on the test results, except for a few specific instances. Other variables, such as the presence of anticoagulants in the specimen and sample discoloration due to hemolysis, hyperbilirubinemia or lipemia were more often responsible for inconsistencies in test results.

Alkaline Phosphatase↗
PubMed1978

Reference values for clinical chemistry using the Coulter Chemistry System.

Reference (normal) ranges were established for clinical chemistry results obtained from the Coulter Chemistry instrument on specimens from dogs, cats, horses, and cattle. These results, in general, are very similar to those reported in the current veterinary literature. The specimens obtained from horses and cows were subdivided according to age and lactation status, respectively. Significant differences were noted between the subgroups in the results of certain tests.

Animals↗
PubMed1978

Special topics in clinical pathology.

The following topics are discussed in this presentation: A. Recent advances in the use and interpretation and methodology of antibiotic susceptibility testing. B. Improvements in sample submittal to obtain accurate results from your laboratory. C. Staining blood, bone marrow, and cytology specimens in the office laboratory. D. Pathogenesis and differential diagnosis of lipemia. E. Differential diagnosis of abdominal effusions.

Alkaline Phosphatase↗
PubMed1977

Equine cerebrospinal fluid: reference values of normal horses.

Cerebrospinal fluid (CSF) samples were collected from the atlanto-occipital (AO) and lumbosacral (LS) subarachnoid spaces of 24 horses and 21 ponies that had no clinical evidence of neurologic disease. Depth of needle insertion, pressures, refractive index, rapid reagent strip test (protein, glucose, blood, pH) results, cell counts, content of protein, glucose, sodium, potassium, chloride, calcium, phosphorus, urea nitrogen, and cholesterol, and activities of creatine phosphokinase, aspartate transaminase, lactic dehydrogenase, and alkaline phosphatase were determined. The resulting clinical reference values obtained were discussed in light of the published normal values for CSF from horses, other animals, and man. White cell counts in CSF were found to be from 0 to 6/microliters. Values for protein content were distributed between wider limits than previously reported values. The LS-AO difference is proposed as a criterion for clinical evaluation of CSF protein content. Ponies were found to have more protein in their CSF than did the horses, and CSF from the LS site contained more glucose than that from the AO site. The CSF electrolyte composition was similar to that of previous reports. Enzyme activities in equine CSF are reported for the 1st time.

Animals↗