From CDC Information Database
This database includes general CDC public health information on specific diseases and health related topics. When available, the database displays genomic information from various CDC web pages. Users are also encouraged to conduct searches of CDC website for additional information.
- The Appropriateness and Cost of Thrombophilia Panel Testing: It’s Complicated
S Bowen et al, CDC Blog Post, December 15, 2016 - Deep Vein Thrombosis and Pulmonary Embolism (DVT/PE) are often underdiagnosed and serious, but preventable medical conditions.
- CDC Challenge Winners!
CDC champions for success in preventing healthcare-associated blood clots. - Deep vein thrombosis/pulmonary embolism are often underdiagnosed and serious, but preventable medical conditions
- Blood Clots and Travel: What You Need to Know
From CDC-Authored Genomics Publication Database
This database contains CDC-authored publications in public health genomics including infectious diseases, newborn screening, reproductive health, genetic testing, cancer, chronic diseases, birth defects and developmental disabilities, environmental and occupational health as well as laboratory, bioinformatics and statistical methods.
- Whole blood gene expression profiles distinguish clinical phenotypes of venous thromboembolism.
Lewis Deborah A et al. Thromb. Res. 2015 Apr 135(4) 659-65 - Family history of myocardial infarction is a risk factor for venous thromboembolism among whites but not among blacks.
Mili Fatima D et al. Clin. Appl. Thromb. Hemost. 19(4) 410-7 - Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks.
Bean Christopher J et al. Thromb. Res. 2012 Dec 130(6) 942-7
From Guideline Database
This database contains updated guidelines, policies and recommendations on genomic research and practice, as provided by professional organizations, federal advisory groups, expert panels and policy groups.
- Recommendations from the EGAPP Working Group: routine testing for Factor V Leiden (R506Q) and prothrombin (20210G>A) mutations in adults with a history of idiopathic venous thromboembolism and their adult family members.
Published 2012 (Evaluation of Genomic Applications in Practice and Prevention) - ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.
Published 2013 (American College of Medical Genetics and Genomics)
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