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1 rs, WHO performance status of 2, or elevated serum lactate dehydrogenase).
2 nced-stage disease, B symptoms, and elevated serum lactate dehydrogenase.
3 ted closely with hemolysis, as determined by serum lactate dehydrogenase.
4 s, abnormal cytogenetics, and high levels of serum lactate dehydrogenase and beta(2)-microglobulin as
5 te count, disease stage, performance status, serum lactate dehydrogenase, and number of extranodal si
6 deletion or 11q deletion by FISH, increased serum lactate dehydrogenase, and unmutated IGHV mutation
8 ow Karnofsky performance status (<80%), high serum lactate dehydrogenase (> 1.5 times upper limit of
9 thrombocytopenia (<20,000/microl), elevated serum lactate dehydrogenase (>1,500U/liter), schistocyto
10 oliferation and apoptosis markers as well as serum lactate dehydrogenase isoenzyme 1 (S-LD-1) may hav
11 opportunistic pneumonia had a higher median serum lactate dehydrogenase (LDH) concentration than did
12 these patients were median age of 56 years; serum lactate dehydrogenase (LDH) greater than 1N, 60%;
14 seen even in the elderly, in those with high serum lactate dehydrogenase (LDH) or beta2-microglobulin
15 ion after CD138 plasma cell purification and serum lactate dehydrogenase (LDH) to evaluate their prog
17 RT-PCR results were also correlated with serum lactate dehydrogenase (LDH), treatment status, and
20 uded WHO performance status (0 v 1 or 2) and serum lactate dehydrogenase (LDH; </= v > 1.5x the upper
22 riable and multivariable analysis, increased serum lactate dehydrogenase level and histology for a me
25 n had poor-risk features defined as elevated serum lactate dehydrogenase level, stage IV, and bulky m
31 e frequent in patients with normal levels of serum lactate dehydrogenase, no bone marrow involvement,
32 btype, and correlated with disease stage and serum lactate dehydrogenase (R(s) = 0.79, P < .001).
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