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1 age histologically and by elevation of serum aspartate transaminase.
2 ive hepatocyte damage and elevation of serum aspartate transaminase.
6 LD activity score, steatosis, triglycerides, aspartate transaminase, alanine transaminase, and stella
7 tinine and blood urea nitrogen) and hepatic (aspartate transaminase, alanine transaminase, and total
8 significant increases in the serum levels of aspartate transaminase, alanine transaminase, blood urea
9 (P =.002), diabetes mellitus (P =.009), and aspartate transaminase/alanine transaminase (AST/ALT) ra
10 ase level greater than 30 U/L, and (3) serum aspartate transaminase/alanine transaminase level less t
13 lesterol, uric acid, and the hepatic enzymes aspartate transaminase and alanine transaminase were sig
14 al (creatinine and cystatin-C), and hepatic (aspartate transaminase and alanine transaminase) damage
15 in BCAT1 activity, but also by reductions in aspartate transaminase and glutamate dehydrogenase activ
16 ng had significantly reduced levels of serum aspartate transaminase and tumor necrosis factor-alpha,
17 rved in serum aminotransferases (alanine and aspartate transaminases) and lactate dehydrogenase level
19 with other renal injury markers (creatinine, aspartate transaminase, and heart-type fatty acid bindin
20 lower peak serum alanine transaminase (ALT), aspartate transaminase, and higher peak serum alkaline p
21 acebo, levels of gamma-glutamyl transferase, aspartate transaminase, and soluble tumor necrosis facto
22 of apoptotic hepatocytes, serum alanine and aspartate transaminases, and DNA fragments in the cytoso
23 ignificant difference in peak serum alanine, aspartate transaminases, and lactate dehydrogenase after
25 lirubin (0.9 +/- 0.1 vs. 1 +/- 0.1, P =.07), aspartate transaminase (AST) (58 +/- 5 vs. 56 +/- 6, P =
28 (-/-) mice manifested as profoundly elevated aspartate transaminase (AST) and alanine transaminase (A
29 ated by using a model enzyme pair comprising aspartate transaminase (AST) and malic dehydrogenase.
30 lammation (CLNI) associated with an elevated aspartate transaminase (AST) level and portal tract feat
31 vealed that recipient age, serum creatinine, aspartate transaminase (AST) level, presence of edema, d
32 chemia/reperfusion (IR) injury with 24 hours aspartate transaminase (AST) levels >2000 IU/L (Group A)
33 HCV infection associated with elevated serum aspartate transaminase (AST) levels predicted the develo
38 iption polymerase chain reaction) as well as aspartate transaminase (AST), alanine transaminase (ALT)
39 r greater were associated with elevated ALT, aspartate transaminase (AST), and gamma-glutamyl transpe
40 liver enzymes, alanine transaminase (ALT) or aspartate transaminase (AST), are commonly used in clini
41 une hepatitis (AIH) by lower serum levels of aspartate transaminase (AST), gamma-globulin, and immuno
42 change from baseline was found in mean ALT, aspartate transaminase (AST), GGT, bilirubin, triglyceri
45 markers of hepatic parenchymal injury (e.g., aspartate transaminase [AST], lactate dehydrogenase [LDH
46 epatic enzymes (alanine transferase, ALT and aspartate transaminase, AST) were only significantly obs
47 elevations in alanine amino transferase and aspartate transaminase at this dose level indicate that
49 nor age, steatosis, cold ischemic time, peak aspartate transaminase, day 5 bilirubin or international
53 (32%), alanine transaminase increase (20%), aspartate transaminase increase (15%), anemia and thromb
54 ount, urea, bilirubin, alanine transaminase, aspartate transaminase, international normalized ratio,
56 Time to significant fibrosis (defined as an aspartate transaminase level to platelet count ratio ind
58 on for 4 weeks significantly increased serum aspartate transaminase levels and hepatic pathology scor
62 otoxicity (grade 3 or 4 change in alanine or aspartate transaminase levels) among 568 patients receiv
68 297 +/- 56, PUGNAc: 126 +/- 21 IU, p < .05), aspartate transaminase (sham surgery: 536 +/- 110, contr
69 including either end-stage liver disease or aspartate transaminase to platelet ratio index (APRI) of
70 og creatinine, log alanine transaminase, log aspartate transaminase, UNOS status, donor gender, and w
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