scholarly journals Comparison of serum creatine kinase and aspartate aminotransferase activity in dogs with Neospora meningoencephalitis and noninfectious meningoencephalitis

Author(s):  
Bethan S. Jones ◽  
Tom Harcourt‐Brown
2010 ◽  
Vol 27 (S18) ◽  
pp. 243-247 ◽  
Author(s):  
P. D. SICILIANO ◽  
L. M. LAWRENCE ◽  
KRISTIN DANIELSEN ◽  
DEBRA M. POWELL ◽  
K. N. THOMPSON

Author(s):  
A. Moolchandani ◽  
M. Sareen

This study was carried out to assess the effects of draft load on serum creatine kinase and lactated ehydorgenase activities in mule. Five adult mules of 5 to 6 years of age were subjected to loading exercise (i.e. 10% draft load for 1 to 5 days and 20% draft load from 6th to 10th day). A highly significant (P<0.01) increase in serum LDH activities in response to 10% and 20% draft load exercise was observed while significant (P<0.05) increase at 10% draft load and highly significant (P<0.01) increase at 20% draft load was observed in CK activities.


1991 ◽  
Vol 20 (6) ◽  
pp. 290-294
Author(s):  
R.E. Weller ◽  
R.L. Buschbom ◽  
S.L. Martell ◽  
J.F. Baer ◽  
C.A. Málaga ◽  
...  

Author(s):  
Maren Freigang ◽  
Claudia D. Wurster ◽  
Tim Hagenacker ◽  
Benjamin Stolte ◽  
Markus Weiler ◽  
...  

1986 ◽  
Vol 32 (10) ◽  
pp. 1901-1905 ◽  
Author(s):  
J C Koedam ◽  
G M Steentjes ◽  
S Buitenhuis ◽  
E Schmidt ◽  
R Klauke

Abstract We produced three batches of a human-serum-based enzyme reference material (ERM) enriched with human aspartate aminotransferase (EC 2.6.1.1), alanine aminotransferase (EC 2.6.1.2), creatine kinase (EC 2.7.3.2), and lactate dehydrogenase (EC 1.1.1.27). The added enzymes were not exhaustively purified; thus the final ERMs contained some enzymes as contaminants, of which only glutamate dehydrogenase activity might interfere. The stability during storage and after reconstitution was good. The commutability of the four enzymes in the three ERM batches was also good, except when German or Scandinavian methods for aminotransferases were involved. The temperature-conversion factors for the ERMs were equivalent to those for patients' sera. Reactivation after reconstitution was complete within 5 min and was independent of the temperature of the reconstitution fluid. We believe that these secondary ERMs will aid in the transfer of accuracy between well-defined reference methods and daily working methods so that clinical enzymology results will become more comparable from laboratory to laboratory.


Author(s):  
Won Tae Bae ◽  
Jae Hui Kim ◽  
Eun Sil Park ◽  
Ji Hyun Seo ◽  
Jae Young Lim ◽  
...  

1976 ◽  
Vol 9 ◽  
pp. 237-240 ◽  
Author(s):  
J.C. Crawhall ◽  
G. Tolis ◽  
D. Roy

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