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Showing search results for "algorithm" 91-100 of 312

  1. ANA Screen,IFA, with Reflex to Titer and Pattern/Systemic Sclerosis Panel 1

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

  2. Gaucher Disease, DNA Mutation Analysis

    Gaucher Disease is an autosomal recessive lysosomal storage disease that leads to the accumulation of glucocerebroside in tissues. Approximately 1 in 10 individuals of Ashkenazi Jewish heritage is a carrier. Treatment …... More

  3. GlycoMark

    GlycoMark CPT Code(s) 84378 Methodology Colorimetric (C) Enzymatic Reference Range(s) 1 Year Not established 2-17 Years Male 15.0-38.0 mcg/mL 2-17 Years Female 11.2-35.7 mcg/mL 18 Years Male…... More

  4. Acute Myeloid Leukemia Prognostic Panel (Normal Karyotype)

    This testing, consisting of FLT3, NPM-1, and CEBPA, is recommended in the NCCN guidelines for determination of AML risk status in patients with cytogenetically normal AML. The presence of CEBPA gene mutations is …... More

  5. B-Type Natriuretic Peptide (BNP)

    BNP is increased in congestive heart failure, left ventricular hypertrophy, acute myocardial infarction, coronary angioplasty, and hypertension. Elevations are also observed in pulmonary hypertension (indicating right …... More

  6. BRCAvantage, Comprehensive

    This test detects mutations in the BRCA1 and BRCA2 genes which are the most common causes of hereditary breast and ovarian cancers.... More

  7. BRCAvantage, Ashkenazi Jewish Screen w/Reflex BRCAvantage, Comprehensive

    This reflexive test screens for 3 mutations within BRCA1 and BRCA2 that are commonly found in the Ashkenazi Jewish population. If the results are negative, the test will reflex to comprehensive testing of the BRCA1 and …... More

  8. 11-Deoxycortisol, LC/MS/MS

    11-Deoxycortisol (Compound S) is useful in diagnosing patients with 11-beta-hydroxylase deficiency (second leading cause of congenital adrenal hyperplasia) and primary (adrenal failure) or secondary (hypothalamic-…... More

  9. Babesia microti DNA, Real-Time PCR

    Babesia microti DNA PCR is a highly specific and sensitive method to detect the presence of B. microti DNA in clinical specimens; DNA sequences from the closely related canine pathogen B. gibsoni are not detected …... More

  10. BRAF Mutation Analysis

    BRAF encodes a serine/threonin protein kinase downstream of the epidermal growth factor receptor (EGFR) and the RAS family of small G-proteins (KRAS, HRAS and NRAS) in the MAPK pathway. BRAF is mutated in approximately …... More

* The tests listed by specialist are a select group of tests offered. For a complete list of Quest Diagnostics tests, please refer to our Directory of Services.