About: Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures

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About: Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) im Jahr 2005 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована в листопаді 2005 (uk)
publication date	wds:Q62978214-19F0E909-D070-4804-90A8-693042C178F0
publication date	2005-01-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q62978214-15BD19F9-D704-4420-82EA-175915A47D73
exact match	https://scigraph.springernature.com/pub.10.1007/s10689-005-0658-9
cites work	wds:Q62978214-0ECC3021-99E3-4CE0-A501-269EE7E2E1DE wds:Q62978214-1CA2A28E-2BAF-440D-99C9-89125F6A0581 wds:Q62978214-230A1902-168D-431F-AEB2-81584DCB1863 wds:Q62978214-3D203251-34E1-41CF-9898-30FE0AD54B6A wds:Q62978214-48FAE398-699D-48EF-9096-1B1B4C3F0EDB wds:Q62978214-6522C287-4650-4FC7-AE49-2D5C4D7F53C5 wds:Q62978214-82D9CA0E-9447-4224-99CA-21340B2918EC wds:Q62978214-89FD6324-761F-4054-B27F-C807B0F6A578 wds:Q62978214-9E16E6FA-B730-44E8-90AC-8E1CB63015DC wds:Q62978214-B84588C8-2135-4B0A-AE67-FA6F2B11C18E wds:Q62978214-C2FF8478-8C14-49F9-B081-6E9C5AE8F96D wds:Q62978214-C79C23F3-5148-4DB0-A041-230F053B3CF3 wds:Q62978214-CC6922ED-36EA-4A72-8E7C-D467868BBC27 wds:Q62978214-EA807829-DCCB-417D-A8C5-152CFBC60ED0 wds:Q62978214-EBB6FB82-17F3-4852-9718-7590C7FF43AD wds:Q62978214-FBFC63C4-803C-408C-B826-132E78C3CF3F wds:Q62978214-FF5E7C16-AF59-4579-96AC-947056ABEDCC
cites work	Psychological and behavioral implications of abnormal mammograms. Cancer risk associated with germline DNA mismatch repair gene mutations Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Comprehension of cancer risk one and 12 months after predictive genetic testing for hereditary non-polyposis colorectal cancer Personal theories of inheritance, coping strategies, risk perception and engagement in hereditary non-polyposis colon cancer families offered genetic testing. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer Cancer risk in mutation carriers of DNA-mismatch-repair genes The outcome of endometrial carcinoma surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred. Colon cancer screening Colon cancer screening practices after genetic counseling and testing for hereditary nonpolyposis colorectal cancer. Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families. No Support for Endoscopic Surveillance for Gastric Cancer in Hereditary Non-Polyposis Colorectal Cancer
author name string	wds:Q62978214-05370C5C-14C8-4430-89BD-DD10F1576AC3 wds:Q62978214-2A8BB84E-9BD7-4C04-8C7A-719B8922C6C4 wds:Q62978214-31CEAC48-41FE-4458-B703-9812A69620A6 wds:Q62978214-8CC7F0CC-D9F0-4D92-A549-9EE7D2817B4F wds:Q62978214-92487416-5627-4C6A-99FE-7728C05499E7 wds:Q62978214-A676EC53-4564-47AD-A29D-DE37170E7641 wds:Q62978214-B8D7C7EA-F450-466E-AD51-4AC5194CFE14 wds:Q62978214-BD785A3F-C3C8-49F2-B7FF-13C5EFD9E4A4
author name string	Hanne Meijers-Heijboer Anja Wagner Carli M J Tops Conny A van der Meer Juul Th Wijnen Ingrid van Kessel Iris I H van Oostrom Mieke G Kriege
rdfs:label	Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures (en) Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures (nl)
skos:prefLabel	Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures (en) Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures (nl)
name	Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures (en) Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures (nl)
author	wds:Q62978214-6FC4A52B-66A1-4CEC-AC9F-F31BFB713EE8
author	Hans Vasen
title	wds:Q62978214-89D9E6B6-4EED-413B-8C7B-8D9936B797AE
title	Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures (en)
page(s)	wds:Q62978214-BF85B3F8-B0EF-4449-B0C2-CC3A6B7FE96D
page(s)	295-300
instance of	wds:Q62978214-A5E0DA6D-4188-4A13-A8C0-3AA1FCAD3C3B
instance of	scholarly article
main subject	wds:Q62978214-D956540D-BA22-4758-9D02-68BC69D445D3
main subject	Lynch syndrome
PubMed ID	wds:Q62978214-F4F17DEA-8B38-4D68-A70F-60F66B4585F2
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16341806
PubMed ID	16341806
published in	wds:Q62978214-058B1474-BF79-451B-86C9-30234EC6F9A7
published in	Familial Cancer
issue	wds:Q62978214-4057D73E-122F-401A-97CC-2F5E4DC23B69
volume	wds:Q62978214-29261BD2-576B-43FB-9F8D-53C0FD808F8F
issue	4
volume	4
DOI	wds:Q62978214-A6BCB594-20BC-425A-B858-61E22A6E824E
DOI	http://dx.doi.org/10.1007/S10689-005-0658-9
DOI	10.1007/S10689-005-0658-9
Dimensions Publication ID	wds:Q62978214-CA0504D7-89DE-4A48-AE73-4F1A86ED68C7
Dimensions Publication ID	1019202692
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q62978214
is cites work of	Prevalence of alterations in DNA mismatch repair genes in patients with young-onset colorectal cancer Living with hereditary non-polyposis colorectal cancer; experiences from and impact of genetic testing. Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population. Prevalence and predictors of appropriate colorectal cancer surveillance in Lynch syndrome. Sharing genetic test results in Lynch syndrome: communication with close and distant relatives EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome Development and pilot testing of two decision aids for individuals considering genetic testing for cancer risk

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