Detalhe da pesquisa
1.
Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group.
J Med Genet
; 59(4): 318-327, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33622763
2.
Risk assessment and genetic counseling for Lynch syndrome - Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
J Genet Couns
; 31(3): 568-583, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35001450
3.
Prevalence of Germline Mutations in Polyposis and Colorectal Cancer-Associated Genes in Patients With Multiple Colorectal Polyps.
Clin Gastroenterol Hepatol
; 17(10): 2008-2015.e3, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30557735
4.
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome.
Genet Med
; 21(12): 2706-2712, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31204389
5.
Somatic TP53 variants frequently confound germ-line testing results.
Genet Med
; 20(8): 809-816, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29189820
6.
Gastrointestinal Polyposis in Cowden Syndrome.
J Clin Gastroenterol
; 51(7): e60-e67, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27661969
7.
Effect of Sulindac and Erlotinib vs Placebo on Duodenal Neoplasia in Familial Adenomatous Polyposis: A Randomized Clinical Trial.
JAMA
; 315(12): 1266-75, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27002448
8.
Colorectal Cancer Screening, Version 1.2015.
J Natl Compr Canc Netw
; 13(8): 959-68; quiz 968, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26285241
9.
Esophageal and esophagogastric junction cancers, version 1.2015.
J Natl Compr Canc Netw
; 13(2): 194-227, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25691612
10.
Hereditary and common familial colorectal cancer: evidence for colorectal screening.
Dig Dis Sci
; 60(3): 734-47, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25501924
11.
Creation of a network to promote universal screening for Lynch syndrome: the LynchSyndrome Screening Network.
J Genet Couns
; 24(3): 421-7, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25220566
12.
Colon Pathology Characteristics in Li-Fraumeni Syndrome.
Clin Gastroenterol Hepatol
; 16(1): 140-141, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28624650
13.
Colorectal cancer screening.
J Natl Compr Canc Netw
; 11(12): 1538-75, 2013 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24335688
14.
Serrated polyposis: colonic phenotype, extracolonic features, and familial risk in a large cohort.
Dis Colon Rectum
; 56(11): 1211-6, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24104994
15.
Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting.
Genet Med
; 14(1): 152-62, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22237445
16.
Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline.
J Genet Couns
; 21(4): 484-93, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22167527
17.
Universal Germline Panel Testing for Individuals With Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield.
J Clin Endocrinol Metab
; 107(5): e1917-e1923, 2022 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35026032
18.
Hereditary and familial colon cancer.
Gastroenterology
; 138(6): 2044-58, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20420945
19.
Letter to the editor: mistaken inheritance.
Int J Colorectal Dis
; 31(3): 711-2, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25847823
20.
Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer.
Fam Cancer
; 18(1): 105-108, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29785566