Detalhe da pesquisa
1.
Delineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndrome.
Genes Chromosomes Cancer
; 63(5): e23237, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38722212
2.
Molecular and Clinicopathologic Characterization of Mismatch Repair-Deficient Endometrial Carcinoma Not Related to MLH1 Promoter Hypermethylation.
Mod Pathol
; 37(3): 100423, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38191122
3.
Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision.
Br J Surg
; 111(5)2024 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38722804
4.
Enrichment of colibactin-associated mutational signatures in unexplained colorectal polyposis patients.
BMC Cancer
; 24(1): 104, 2024 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38238650
5.
Relation between WHO Classification and Location- and Functionality-Based Classifications of Neuroendocrine Neoplasms of the Digestive Tract.
Neuroendocrinology
; 114(2): 120-133, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-37690447
6.
Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant Carriers.
Mod Pathol
; 36(9): 100240, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37307877
7.
Universal Immunohistochemistry for Lynch Syndrome: A Systematic Review and Meta-analysis of 58,580 Colorectal Carcinomas.
Clin Gastroenterol Hepatol
; 20(3): e496-e507, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33887476
8.
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
Hered Cancer Clin Pract
; 20(1): 36, 2022 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36182917
9.
The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance.
Int J Cancer
; 148(4): 800-811, 2021 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32683684
10.
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
Genet Med
; 23(4): 705-712, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33257847
11.
The coding microsatellite mutation profile of PMS2-deficient colorectal cancer.
Exp Mol Pathol
; 122: 104668, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34302852
12.
Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer.
Genes Chromosomes Cancer
; 2020 Jul 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32615015
13.
Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy.
J Med Genet
; 56(2): 53-62, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30415209
14.
Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome-Associated Colorectal Carcinomas.
Gastroenterology
; 165(1): 271-274.e2, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-36931573
15.
Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2.
Gastroenterology
; 155(3): 844-851, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29758216
16.
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
17.
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report.
Hered Cancer Clin Pract
; 17: 28, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31636762
18.
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.
Hered Cancer Clin Pract
; 17: 8, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30858900
19.
APC mosaicism, not always isolated: two first-degree relatives with apparently distinct APC mosaicism.
Gut
; 72(11): 2186-2187, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36307181
20.
Distinct Patterns of Somatic Mosaicism in the APC Gene in Neoplasms From Patients With Unexplained Adenomatous Polyposis.
Gastroenterology
; 152(3): 546-549.e3, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27816598