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Showing search results for "algorithm" 21-30 of 314

  1. Antithrombin III Activity

    Antithrombin III Activity CPT Code(s) 85300 Methodology Chromogenic Substrate Limitations Expected impact by therapeutic levels (potential interference depends upon drug concentration): Warfarin: no effect; Heparin (UFH…... More

  2. Antiphospholipid Syndrome Diagnostic Panel

    This assay may be useful in supporting or ruling out a diagnosis of antiphospholipid syndrome.... More

  3. Cardiolipin Antibody (IgM)

    Cardiolipin antibodies (CA) are seen in a subgroup of patients with autoimmune disorders, particularly Systemic Lupus Erythematosus (SLE), who are at risk for vascular thrombosis, thrombocytopenia, cerebral infarct and/…... More

  4. Cardiolipin Antibody (IgG)

    Cardiolipin antibodies (CA) are seen in a subgroup of patients with autoimmune disorders, particularly Systemic Lupus Erythematosus (SLE), who are at risk for vascular thrombosis, thrombocytopenia, cerebral infarct and/…... More

  5. JAK2 V617F Mutation, Quantitative, Plasma-Based, Leumeta

    The JAK2 tyrosine kinase (V617F) was detected in most patients ( 80%) with polycythemia vera (PV), 30-50% of patients with either essential thrombocythemia (ET) or myelofibrosis. The Quantitative measurement of V617F …... More

  6. Antiphospholipid Syndrome Diagnostic Panel

    This assay may be useful in supporting or ruling out a diagnosis of antiphospholipid syndrome.... More

  7. Antithrombin III Antigen

    A decrease in Antithrombin III may predispose an individual to thrombosis and to failure to respond to heparin therapy. This can occur as a result of a congenital deficiency, secondary to liver transplant, DIC, …... More

  8. BCR-ABL1 Gene Rearrangement, Quantitative, PCR

    This reverse-transcription PCR-based assay detects the BCR-ABL1 transcript produced by the t(9;22) chromosomal translocation associated with chronic myelogenous leukemia (CML) and a subset of lymphoblastic leukemias. …... More

  9. Activated Protein C-Resistance

    Activated Protein C (APC) resistance is the most frequent hereditary defect associated with deep vein thrombosis. Over 95% of the APC resistance phenotype is due to the Factor V Leiden Mutation. The APC-resistance assay…... More

  10. Beta-2-Glycoprotein I Antibody (IgM)

    Beta-2-Glycoprotein 1, apolipoprotein H, is a cofactor in antiphospholipid antibody binding and is the critical antigen in the antiphospholipid antibody syndrome. Beta-2-Glycoprotein 1 Antibody is more specific than …... More

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