Highsmith, Jr. / Highsmith / Jr. Molecular Diagnostics

12 Tests That Changed Everything
1. Auflage 2013
ISBN: 978-1-4614-8127-0
Verlag: Springer US
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, 257 Seiten, eBook

Reihe: Molecular and Translational Medicine

Molecular Diagnostics: 12 Tests That Changed Everything focuses on specific laboratory tests and emphasizes how the availability of these tests has altered how clinicians treat their patients.  Presented as a standard outline, each chapter focuses on a specific molecular test  and provides background on the test and its clinical applications. Continuing with some discussion on how the test is done, interpreted, and used clinically, each chapter then concludes with a discussion of how that test has changed the way medicine is practiced with respect to the disease or condition in question.Authored by renowned experts in the field, Molecular Diagnostics: 12 Tests That Changed Everything is a valuable resource for pathologists, pathology residents, laboratory directors, development personnel, lab medicine fellows and those working in the broad area of oncology, infectious disease and genetics.

Zielgruppe

Professional/practitioner

Autoren/Hrsg.

Jr.,

Highsmith, Jr., W. Edward

Highsmith, Jr.

Inhaltsverzeichnis

Clinical FISH Testing for the Diagnosis of Solid Tumors.- Epidermal Growth Factor Receptor Testing in Lung Adenocarcinoma.- The Human Epidermal Growth Factor Receptor 2 (HER2).- Tamoxifen and Irinotecan Pharmacogenomics.- Hepatitis C Virus Testing.- Laboratory Testing for HIV Infection: Advances after 27 years.- Detection of Herpes Simplex Virus in Cerebrospinal Fluid using Real-time PCR.- Toward a Safer Blood Supply: The Impact of Molecular Testing.- Chromosomal Microarrays.- BRCA1 and BRCA2 Testing in Inherited Breast Cancer.- Cystic Fibrosis: Carrier Testing, Newborn Screening, and Diagnostic Testing.- Newborn Screening by Tandem Mass Spectrometry and Molecular Confirmation.- Next Generation Clinical Diagnostics: The Sequence of Events.

Über Autor(innen)

W. Edward Highsmith, Jr., PhD Mayo Clinic College of Medicine, Department of Laboratory Medicine and Pathology, Molecular Genetics Laboratory, Rochester, MN, USA