Fourfold increased detection of Lynch syndrome by raising age limit for tumour genetic testing from 50 to 70 years is cost-effective.
暂无分享,去创建一个
[1] J. Balmaña,et al. Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines. , 2013, Annals of oncology : official journal of the European Society for Medical Oncology.
[2] Marc S. Williams,et al. Impact of age cutoffs on a lynch syndrome screening program. , 2013, Journal of oncology practice.
[3] F. Nagengast,et al. Familial colorectal cancer risk assessment needs improvement for more effective cancer prevention in relatives , 2013, Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland.
[4] P. Møller,et al. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts , 2013, Gut.
[5] J. Stockman,et al. Strategies to Identify the Lynch Syndrome Among Patients With Colorectal Cancer: A Cost-Effectiveness Analysis , 2013 .
[6] J. Potter,et al. Identification of Lynch syndrome among patients with colorectal cancer. , 2012, JAMA.
[7] E. Kuipers,et al. Yield of routine molecular analyses in colorectal cancer patients ≤70 years to detect underlying Lynch syndrome , 2012, The Journal of pathology.
[8] I. Nagtegaal,et al. Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome. , 2011, European journal of cancer.
[9] Heather Hampel,et al. The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer , 2010, Genetics in Medicine.
[10] Jukka-Pekka Mecklin,et al. Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[11] H T Lynch,et al. Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications , 2009, Clinical genetics.
[12] Suet Yi Leung,et al. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1 , 2009, Nature Genetics.
[13] Heather Hampel,et al. Feasibility of screening for Lynch syndrome among patients with colorectal cancer. , 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[14] F. Radvanyi,et al. Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based Approach Versus Molecular Screening , 2008, The American Journal of Gastroenterology.
[15] M. Ligtenberg,et al. Interpretation of Immunohistochemistry for Mismatch Repair Proteins is Only Reliable in a Specialized Setting , 2008, The American journal of surgical pathology.
[16] A. W. Musschenga. Zinnige en duurzame zorg , 2007 .
[17] H. Meijers-Heijboer,et al. Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures , 2005, Familial Cancer.
[18] W. Frankel,et al. Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). , 2005, The New England journal of medicine.
[19] T. Ruers,et al. Cost effectiveness of a new strategy to identify HNPCC patients , 2004, Gut.
[20] Sudhir Srivastava,et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. , 2004, Journal of the National Cancer Institute.
[21] A. Cats,et al. Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect , 2003, Gut.
[22] W. Zoller,et al. [Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer]. , 2001, Zeitschrift fur Gastroenterologie.
[23] H T Lynch,et al. New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. , 1999, Gastroenterology.
[24] Deborah Schrag,et al. Benefits of Colonoscopic Surveillance and Prophylactic Colectomy in Patients with Hereditary Nonpolyposis Colorectal Cancer Mutations , 1998, Annals of Internal Medicine.
[25] S Srivastava,et al. A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. , 1998, Cancer research.
[26] THE HAGUE-THE NETHERLANDS , 2022 .