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Based on ticlopidine active as an ADP receptor antagonist for inhibiting platelet aggregation in clinical test, and upon finding -1,2-substituted-7-sulfonylamide/amide-1,2,3,4-tetrahydroisoquinoline (11–31) inhibited of platelet aggregation, a series of -1-o-chlorophenyl-2-substituted-tetrahydroisoquinoline derivativesynthesizedned and synthesized.
These individuals are completely deficient in BuChE but have only minor abnormalities in clinical test results [34], [35].
Any marked abnormalities in clinical test results or vital signs were assessed for clinical significance by the investigator.
Most risk factors have been assessed in laboratory settings or in clinical test situations, and fall risk assessment tools have been developed based on these assessments [ 3– 6].
To overcome this limitation of bare BMVC staining in clinical test, it is critical to eliminate dead cells for BMVC test to prevent false positive.
Using BMVC test for the detection of malignant pleural effusions, we overcame the limitations of bare BMVC staining in clinical test and reduced the ambiguity in morphological interpretation of cytologic smear due to intra-observer or inter-observer variability.
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