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This "Specialty Testing" webinar will provide an overview of evidence-based applications of pharmacogenomics, share recent advances, and discuss the clinical utility of new panels and single-gene tests.
This "Specialty Testing" webinar will outline the benefits and limitations of genetic testing for neurologic disorders and provide a framework for interpretation of test results.
This “Specialty Testing” webinar discusses changes introduced in the 8th edition of the AJCC lung cancer staging manual.
This "Specialty Testing" webinar will discuss what ceramides are and how they link to atherosclerosis and cardiovascular disease processes.
This "Specialty Testing" webinar explains the causes of hereditary and acquired erythrocytosis, discuss methods for diagnosis, and share cases for illustration.
This "Specialty Testing" webinar will provide an overview of novel biomarker discoveries and advances being made in the study of autoimmune gliopathies.
In this "Specialty Testing" webinar, the experts at Mayo Medical Laboratories have put together knowledge, tools, and resources to assist organizations in the efforts of maintaining clinical quality and achieving value as they pursue a request for proposal (RFP) in the reference laboratory space.
This "Specialty Testing" webinar will outline the different tests to detect patients who are at risk for thiopurine-related toxicity and the advantages of each test.
This "Specialty Testing" webinar addresses complement testing. It has acquired considerable clinical popularity in recent times. An overview of the complement system, pre-analytical challenges, and modern laboratory testing will be presented.
This "Specialty Testing" webinar describes a new serum test for bile acid malabsorption. Descriptions illustrate how the test can be used as a screening test and as a tool for therapeutic action.
In this "Specialty Testing" webinar we have an educational overview of the large category of peripheral neuropathies, discussing various testing platforms and their strengths and weaknesses, with a focus on identifying hereditary neuropathies.